@article {2550, title = {Association Between Contraceptive Use and Pap Smear Findings in PKK Women in Bendul Merisi Surabaya}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {September 2025}, pages = {642-643}, type = {Original Article}, chapter = {642}, abstract = {

Background: Cervical cancer remains a major health burden for women worldwide. Pap smear is a widely used screening tool, while contraceptive use, particularly hormonal methods, has been debated as a potential risk factor for cervical lesions. Objective: This study aimed to investigate the association between contraceptive use and Pap smear findings among members of the Family Welfare Movement (PKK) in Bendul Merisi, Surabaya. Methods: A cross-sectional study was conducted involving 64 respondents selected through purposive sampling. Data were collected using questionnaires and Pap smear results. Statistical analysis was performed using contingency coefficient tests. Results: The study revealed a significant association between contraceptive use and Pap smear results (p = 0.001). Different types and duration of contraceptive use were significantly related to cytological outcomes, with hormonal methods showing a stronger association with abnormal findings such as LSIL (Low-grade Squamous Intraepithelial Lesion). Conclusions: Contraceptive use, especially hormonal methods with longer duration, influences Pap smear findings, highlighting the need for regular cervical cancer screening among women using hormonal contraception

}, keywords = {Cervical cancer, Contraceptives, Cytology, Pap Smear, Uterine Cervix}, doi = {10.5530/pj.2025.17.80}, author = {Nefertiti EP and Sudiarta KE and Redemptus Y and Biutifasari V} } @article {2490, title = {Chemical Composition and Nutritional Value of Edible Moroccan Truffles}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {April 2025}, pages = {211-216}, type = {Original Article}, chapter = {211}, abstract = {

Background and objectives: Truffles have a unique nutritional profile and are known to play an important role in terrestrial ecosystems. Mediterranean countries, including Morocco, are the location of an abundant harvest of truffles. This study investigated the chemical composition and the nutritional value of edible Moroccan truffles. Materials and methods: We studied the nutritional profile, and we performed a phytochemical screening of Tirmania pinoyi, Terfezia claveryi, Terfezia oligosperma, Terfezia rosea, and Terfezia arenaria collected from different areas from Morocco. Results and conclusions: The results showed that the truffles that we analyzed are a good source of carbohydrates, lipids and dietary fibers. The phytochemical screening that we performed afterwards revealed that these Moroccan truffles contain numerous secondary metabolites such as saponins, alkaloids, sterols, coumarins, and tannins. These results demonstrate the nutritional value of these truffles that can support a healthy and well-balanced diet. The secondary metabolites that we detected in our samples can make an important pharmacological contribution that could be the subject of future investigations for therapeutic purposes.

}, keywords = {Fungi, Morocco, Nutritional Value, Phytochemical screening, Truffles}, doi = {10.5530/pj.2025.17.26}, author = {Lamyae Yachi and Soukaina Bennis and Madiha Alami Chentoufi and Mohamed Yafout and Brahim Mojemmi and Amal Ait Haj Said and Mustapha Bouatia} } @article {2573, title = {Preclinical Safety Assessment of a Polyherbal Formulation: Acute, Subchronic, and Mutagenic Evaluation}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {December 2025}, pages = {322-328}, type = {Original Article}, chapter = {322}, abstract = {

Introduction: Before market approval, novel herbal medicines and bioactive compounds require rigorous genotoxicity and safety evaluations. A polyherbal formulation derived from Dasiphora fruticosa, Cynara scolymus, and Rosa acicularis has previously demonstrated antioxidant and nephroprotective properties. However, comprehensive toxicological and mutagenicity evaluations are needed to support its clinical development. In this study, we aimed to evaluate the acute and subchronic toxicities and mutagenic potential of this polyherbal formulation. Methods: Acute oral toxicity was assessed in C57BL/6 mice using a two-phase protocol based on Lorke{\textquoteright}s method. Subchronic toxicity was evaluated in Wistar rats following OECD guideline 407, with daily oral administration of the polyherbal formulation at doses of 500 and 1,000 mg/kg for 28 days. Mutagenicity was assessed using the Muta-Chromoplate (Ames test) kit according to OECD guideline 471. Results: Acute toxicity evaluation determined that the median lethal dose (LD50) of the polyherbal formulation exceeds 5,000 mg/kg, categorising it as practically nontoxic. The subchronic toxicity assessment revealed that doses of 500 and 1,000 mg/kg had no significant effects on body and organ weight, haematological and biochemical parameters, and histopathological features compared with the controls. Furthermore, the Ames test confirmed that the polyherbal formulation had no mutagenic activity. Conclusions: The polyherbal formulation exhibited no acute toxicity at doses up to 5,000 mg/kg, and no adverse effects were observed in a 28-day subchronic toxicity study. Furthermore, its favourable safety profile was further confirmed by its lack of mutagenic potential. Collectively, these findings provide a robust foundation for continued preclinical and clinical development of the polyherbal formulation

}, keywords = {acute toxicity; mutagenicity; phytochemicals; polyherbal formulation; safety evaluation; subchronic toxicity}, doi = {10.5530/pj.2025.17.102}, author = {Enkhmaa Gonchig and Chimgee Tserendash and Maral-Erdene Gerelt-Od and Batdavaa Batbayar and Mend-Amar Batbaatar and Perleidulam Bunddulam and Enerel Yeruult and Narankhajid Myadagsuren and Otgonbat Altangerel and Yeruult Chultemsuren} } @article {2442, title = {Acute Chemical Eye Injury as Result of an Assault: Clinical and Forensic Approach}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {December 2024}, pages = {1408-1410}, type = {Research Article}, chapter = {1408}, abstract = {

Introduction: Chemical injuries represent a significant health concern, characterized by trauma inflicted by corrosive substances, including both acidic and alkaline agents. Chemical trauma to the eye is particularly critical due to its potential for high morbidity and irreversible blindness, necessitating immediate medical intervention. Understanding clinical aspect of chemical eye injury is crucial, as it not only impacts clinical outcomes but also informs forensic management strategies. Method: Case reports on chemical eye injury case causing by an assault. In-depth study about the case based on clinical aspect of the disease and its management in forensic. Results: Presented male; 56 years old suffered from chemical burns on both eyes causing by suspected acid liquid. The acid was poured on the victim by his biological son. Examination shows limbal ischemia was 270o accompanied by corneal erosion in the right eye. Visual acuity test shows a decrease in vision for both eyes. Litmus examination of the right eye showed a pH of 6 {\textendash} 7. Case management involves collaboration between clinical management by the eye department and legal management correlated to the assault by the forensic department. Conclusion: In a case of chemical assaults to the eyes, clinical management and prognosis of the injury suffered by patient will determine the severity of injury. This in turn, will be one of the considerations for the judges to decide

}, keywords = {Case management, Chemical burns, Eye injury, Forensic medicine}, doi = {10.5530/pj.2024.16.226}, author = {Tia Maya Affrita and Ahmad Yudianto and Syahroni} } @article {2260, title = {Anxiety Levels, Cortisol, Blood Gluc Ose and Sodium Levels in Working Wives: Comparison Between Husbands Who Were Hospitalized and Husbands Who Were Not Hospitalized}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {April 2024}, pages = {382-387}, type = {Research Article}, chapter = {382}, abstract = {

Background:\ Anxiety affects balance and physiological changes in the body. The research aims to investigate the comparison of anxiety levels, blood cortisol levels, blood glucose levels and blood sodium levels between working wives of husbands who are hospitalized and working wives of husbands who are not hospitalized. Methods: The research design uses statistical group comparison. The research subjects were 40 people divided into 2 groups, namely 20 subjects, working wives, husbands who were hospitalized, 20 subjects, working wives, husbands, who were not hospitalized. Data was collected using the HARS (Hamilton Anxiety Rating Scale) questionnaire instrument, laboratory examination of blood cortisol levels, blood glucose levels and blood sodium levels. Results: Unpaired t test with a significant value of p \< 0.05 if the data is normally distributed or Mann Whitney U Test with a significant value of p \< 0.05 if the data is not normally distributed was carried out to analyze the comparison of anxiety levels, blood cortisol levels, sugar levels blood and blood sodium levels. Data processing with the help of statistical software. The results of the analysis showed that there were differences in anxiety levels (p\<0.05), blood cortisol levels (p\<0.05) and blood glucose levels (p\<0.05) but there were no differences in blood sodium levels (p\>0.05). between working wives whose husbands are hospitalized and working wives whose husbands are not hospitalized. Conclusion: blood cortisol levels and blood sugar levels in working wives of husbands who were hospitalized were higher than working wives of husbands who were not hospitalized and based on statistical tests, significant differences were found in HARS values, blood cortisol levels and blood sugar levels between the group of working wives whose husbands were hospitalized. hospitalized and the wife works, the husband is not hospitalized.

}, keywords = {Anxiety, blood cortisol levels, blood glucose levels, blood sodium levels, HARS, working wife}, doi = {10.5530/pj.2024.16.59}, author = {Rudi Mahruzar and I Nyoman Ehrich Lister and OK Yulizal and Hamzah Shatri and Gusbakti Rusip} } @article {2449, title = {Cerebral Vessel Rupture Leading to Sudden Death: Implications for Pharmacognosy}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {December 2024}, pages = {1442-1446}, type = {Case Report}, chapter = {1442}, abstract = {

Sudden death is one of the situations that necessitates immediate treatment from a forensic doctor. The WHO defines sudden death as death occurring within 24 hours of the beginning of symptoms. There are three sorts of sudden death: unexpected, unwitnessed, and spontaneous. Diseases of the Central Nervous System are the third most common cause of sudden death. Ischemic stroke (blockage) and hemorrhagic stroke (bleeding) are examples of central nervous system illnesses. Hypertension (cardiovascular disease) and smoking are known risk factors for hemorrhagic stroke.In 2019, the global incidence of intracerebral hemorrhage (ICH) and subarachnoid hemorrhage (SAH) was 14.46 per 100,000 people. The case discussed in our paper is about the sudden death of a European (Ukrainian) ship captain who happened to be anchored in the waters of Gresik, East Java, who died of hemorrhagic stroke.

}, keywords = {Cardiovascular Disease, ICH, SAH, Stroke, sudden death}, doi = {10.5530/pj.2024.16.233}, author = {Farhad Moegis and Ahmad Yudianto and Renny Sumino} } @article {2396, title = {Effective Dose of Cocoa as a Preemptive Analgesic and Anti- Inflammatory Agent Assessed through Pain Scale and Tumor Necrosis Factor Alpha (TNF-α) in an Acute Pain Animal Model}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {October 2024}, pages = {1134-1137}, type = {Research Article}, chapter = {1134}, abstract = {

Background: Pain is a significant issue for 40-50\% of hospital patients, with 10-50\% of acute pain cases potentially progressing to chronic pain. Pain-associated inflammation often involves the release of mediators, including Tumor Necrosis Factor Alpha (TNF-α). Cocoa beans contain polyphenols, catechins, anthocyanidins, and proanthocyanidins, compounds believed to possess analgesic properties. This study aims to assess cocoa{\textquoteright}s potential as an oral preemptive analgesic agent in an acute pain mouse model, with an emphasis on its impact on inflammation through TNF-α levels. Methods: This true experimental study involved 24 male white mice split into four groups: a control group (K0) receiving a placebo, a treatment group receiving 15 mg/kg BW oral paracetamol (Kpct), a treatment group receiving 0.5 mg/g BW cocoa (K1), and a treatment group receiving 1 mg/g BW cocoa (K2). Pain response was measured using TNF-α levels and the von Frey test. The Kruskal-Wallis test and One-Way ANOVA were employed for statistical analysis. Results: Cocoa at doses of 0.5 mg/g BW and 1 mg/g BW substantially reduced TNF-α levels (75.82 {\textpm} 7.77 and 70.79 {\textpm} 11.50, respectively) compared to the control and paracetamol groups (98.22 {\textpm} 14.74 and 92.81 {\textpm} 2.64). On the first day, compared to the control group{\textquoteright}s 1.82 {\textpm} 0.78 von Frey values, the cocoa-treated groups{\textquoteright} values (6.20 {\textpm} 2.72 and 7.63 {\textpm} 4.11) were notably higher. There were no notable variations in von Frey values across the groups on the second day. However, a correlation was found between von Frey values on the first and second days. Conclusion: Cocoa can potentially serve as an effective preemptive analgesic agent, reducing pain and inflammation primarily by reducing TNF-α levels. These results provide validity to the use of cocoa as an alternative therapy in acute pain management.

}, keywords = {Cocoa, Pain, Pain Degree Analgesia, TNF-α}, doi = {10.5530/pj.2024.16.185}, author = {Herry Cahya Fathani and Herdiani Sulistyo Putri and Prananda Surya Airlangga and Christrijogo Sumartono Waloejo and Ira Sari Yudaniayanti and Pudji Lestari} } @article {2389, title = {Hepato-restorative Activity of Methanolic Extracts of Coccinia grandis L. Voigt. in CCl4 - Intoxicated Rats}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {October 2024}, pages = {1096-1102}, type = {Research Article}, chapter = {1096}, abstract = {

Background: Coccinia grandis has pharmacological activities such as antioxidant, anti-ulcer, antiinflammatory, anti-hypersensitive, anti-hyperglycaemic, anti-cancer and hepatoprotective. Objective: This work is aimed to investigate an alternative low-cost green drug with hepatoprotective potential from methanolic extract of the leaf, stem and their corresponding calli of Coccinia grandis. Materials and Methods: Using 42 Albino Wistar rats divided into seven groups each group containing 6 rats. 1.5ml/kg bw of CCl4 diluted in olive oil was orally injected for fourteen days and methanolic extracts of parent plant parts, callus and silymarin, and on the last day of treatment, experimental rats were anesthetized, blood and organ removed for the biochemical and histopathological analysis. Results: This work is aimed to investigate an alternative low-cost green drug with hepatoprotective potential. Liver damage was induced by CCl4 (1.5 ml/kg body weight) in Wistar albino rats and recovery was noted by treating with Silymarin (100mg/kg bw), a known standard herbal drug and by treating with crude methanolic extract of leaf and stem parts of Coccinia grandis and their corresponding calli (leaf callus and stem callus at 180mg/kg bw) in terms of marked decrease in CCl4- increased SGOT (Serum glutamic oxaloacetic transaminase), SGPT (Serum glutamic pyruvic transaminase), ALP (Alkaline phosphatase), TB (Total bilirubin) and rise in TP (Total protein) compared to untreated control group. Histopathological studies of hepatocytes provide evidence of the centrilobular vacuolar degeneration and recovery by Silymarin or treatment with plant and callus extracts. Conclusion: Biochemical and histopathological examination proved the hepatoprotective potential of calli and parent plant parts (leaf, stem) of Coccinia grandis.

}, keywords = {Callus, CCl4, Coccinia grandis, GC-MS, Liver, Silymarin}, doi = {10.5530/pj.2024.16.178}, author = {Vimala Yerramilli and Mahendra Singh and Ishwar Singh and Laxman Nagar and Jitendra Singh} } @article {2441, title = {Identification of Murder Victims{\textquoteright} Cranial Bone Mutilation Using Forensic Medicine, Anthropology, and Genotype DNA Approaches}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {December 2024}, pages = {1404-1407}, type = {Research Article}, chapter = {1404}, abstract = {

The objective of forensic identification is to aid investigators in ascertaining an individual{\textquoteright}s identity. Reliability in identifying human remains from natural catastrophes, man-made disasters, and situations involving missing individuals has significantly advanced. Anthropological examination and forensic genetic profiling are particularly beneficial when traditional identification procedures, such as fingerprinting or ocular recognition, are not feasible. Even in cases where only skeletal remains are present, anthropological inquiries and forensic genetic examination of the remaining body parts can ascertain the identity and familial connection of the surviving individual. We have found a decapitated skull that is missing its lower jaw and comprises several cervical bones. Investigators think that the decapitated head is a component of a victim who was previously interred. We conducted an autopsy, an anthropological analysis and report the process of identifying skull bone mutilations in murder victims using forensic medicine, anthropology, and DNA genotyping approaches. We performed autopsy and anthropological investigations to collect data from the skeletal remains and a genetic analysis by collecting tooth and blood samples from victims{\textquoteright} parents. These samples were then utilized for DNA extraction, calculation of DNA rate and purity, amplification, and identification of genotype. After investigation, we discovered a single cranial bone and four cervical bones. Under macroscopic examination, the bones exhibit a striking resemblance to the structure of a human head and neck. The presence of tissue still attached to the bones indicates that the time of death exceeds 10 days. The complete destruction of the cranial bones indicates that they belong to individuals aged between 21 and 39 years. The presence of shovel-shaped teeth, a rounded palatal form, straight palatal sutures, and molar teeth with four cusps provide strong identification of the deceased individual as belonging to the Mongoloid race. The assessment of height is challenging due to the absence lengthy bones

}, keywords = {Antrophology, Autopsy, Genetic Profiling, Identification, Skeletal Remains}, doi = {10.5530/pj.2024.16.225}, author = {Setya Aji Priyatna and Satria Perwira and Vernando Parlindungan Simanjuntak and Sari Nur Indahty Purnamaningsih and I Ketut Heru Suryanegara and Desy Martha Panjaitan and Ahmad Yudianto} } @article {2439, title = {Impact of Natural Products and Mindfulness Practices on Serum Serotonin Levels, Clinical Symptoms, and Mindfulness in Adolescents with ADHD Symptoms}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {December 2024}, pages = {1389-1395}, type = {Research Article}, chapter = {1389}, abstract = {

Introduction: Attention Deficit Hyperactivity Disorder (ADHD) is a neurodevelopmental condition marked by impulsivity, hyperactivity, and impaired attention (inattention). Pharmacological treatments are often effective but have limitations, necessitating the exploration of alternative therapies. Interventions based on mindfulness (MBIs) have demonstrated effectiveness in alleviating symptoms of ADHD, but their effects on clinical symptoms, serotonin levels, and mindfulness in adolescents have not been thoroughly studied in Indonesia. This study aimed to evaluate the effectiveness of mindfulness-based interventions on the improvement of clinical symptoms, changes in serum serotonin levels, and mindfulness levels in adolescents with ADHD symptoms. Methods: A true-experimental design with a randomized controlled trial was employed. ADHD symptoms were screened using the Abbreviated Conners{\textquoteright} Teacher Rating Scale (ACTRS) among adolescent students in grades 7 through 9 of junior high school (n = 1067). After meeting all inclusion and exclusion criteria, the study included 28 adolescents aged 12{\textendash}16 years diagnosed with ADHD, divided into treatment (mindfulness) and control groups. Clinical symptoms were assessed using the SPPAHI questionnaire, mindfulness levels were measured with the CAMM scale, and serum serotonin levels were analyzed pre- and post-intervention. Results: The mindfulness group demonstrated notable reductions in clinical symptoms and mindfulness levels in comparison to the control group. There was no notable difference in serum serotonin levels between the two groups. Conclusions: MBIs effectively reduced ADHD symptoms and increased mindfulness levels in adolescents. No substantial changes were observed in serotonin levels, indicating that mindfulness impacts behavioral and cognitive aspects more than biochemical markers. These findings suggest that mindfulness may be a valuable complementary therapy for ADHD management in adolescents.

}, keywords = {CAMM, mindfulness, serotonin serum, SPPAHI}, doi = {10.5530/pj.2024.16.223}, author = {Dianasari and Yunias Setiawati and Royke Tony Kalalo and Atika and Farida Anwari and ASM Morshed and Auliya Yudia Yasyfin} } @article {2430, title = {Plants with Antidiabetic Efficacy among the Dayak Bidayuh Community, Sanggau Regency, West Kalimantan, Indonesia}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {December 2024}, pages = {1342-1348}, type = {Research Article}, chapter = {1342}, abstract = {

Introduction: The use of medicinal plants for diabetes mellitus has been practiced for generations by the Dayak communities in West Kalimantan, Indonesia. The aim of this study is to inventory and describe the utilization of medicinal plants for diabetes mellitus by the Dayak Bidayuh Kerambay, Dayak Golik, and Dayak Sinangkan{\textquoteright}t communities in Sekayam, Beduai, and Entikong Districts, Sanggau Regency, West Kalimantan, Indonesia. Method: This research is a qualitative descriptive study using triangulation method combining interview, observation, and documentation techniques of anti-diabetic mellitus medicinal plants among the Dayak communities. Results: The plants used as anti-diabetic mellitus include Physalis angulata L., Ageratum conyzoides L., Piper betle L., Dillenia suffruticosa (Griff.) Martelli, Syzygium polyanthum (Wight) Walp. Stenochlaena palustris (Burm.f.) Bedd, Gynura procumbens (Lour.) Merr, Curcuma domestica Valeton, Zingiber officinale Rosc., Eleutherine palmifolia (L.) Merr, Curcuma zedoaria (Christm.) Roscoe, Orthosiphon stamineus B., Nepenthes sp., Solanum torvum Swartz, Garcinia mangostana L. The plant parts most commonly used, in sequence, are leaves, rhizomes, roots, fruits, fruit peels, and sometimes the entire plant. The method of preparation for each type of plant is the same, which involves boiling and consuming the boiled decoction. Summary: There are 15 types of plants used by the Dayak tribe community to address diabetes mellitus. Among these 15 types of plants, different parts are utilized, while the processing method remains the same, which is boiling.

}, keywords = {Dayak Bidayuh Tribe, Diabetes mellitus, Medicinal plants}, doi = {10.5530/pj.2024.16.216}, author = {Ruqiah Ganda Putri Panjaitan and Titin and Yohanes Gatot Sutapa Yuliana and Siti Khotimah} } @article {2359, title = {Positive NS1 Antigen in Non-Dengue Virus Infection Serum: Possible Reasons for the Discrepancy with DENV PCR Results}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {August 2024}, pages = {923-926}, type = {Original Article}, chapter = {923}, abstract = {

Background and Objective: A specific examination is required to distinguish between DVI and viral, bacterial, and parasitic illnesses because their clinical manifestations are nearly identical. Leukopenia and lymphocytosis are examples of non-specific tests that might be used to get a diagnosis. Non-structural protein 1 (NS1) antigen, anti-DENV antibody, or DENV-specific nucleic acid detection are more specific assays. Methods: Virus isolation or molecular analysis of the detection of DENV nucleic acid ribonucleic acid (RNA) using RT-PCR was used to make the conclusive diagnosis of DVI. The sensitivity of the DENV RT-PCR method ranges from 28.8 to 99\%. NS1 antigen is used as an initial diagnostic option in primary health care because it has a high specificity value (100\%). Researchers want to analyze the positivity in non-DVI samples that have been confirmed by real-time RT-PCR examination with semi-quantitative NS1 antigen examination. Patient population aged 1-65 years with acute fever \<5 days. A total of 130 samples of non-DVI confirmed patients by RT-PCR were examined for NS1Antigen ELISA. Results: With a proportion of 3.08\% of the total sample, the results showed that 4 NS1Antigen ELISA samples were positive. A negative DENV RT-PCR result could indicate either a true negative or a false negative. Conclusion: The type of PCR technology, the primer used, the existence or absence of a DENV mutation, the DENV serotype, and the presence of mismatched nucleotides can all affect variations in DENV PCR sensitivity.

}, keywords = {Dengue Virus Infection., NS1Ag, RT-PCR DENV}, doi = {10.5530/pj.2024.16.149}, author = {I Gusti Agung Ayu Eka Putri Sunari and Aryati Aryati and Faradila Khoirun Nisa Hakim and May Fanny Tanzilia and Ida Parwati and Rismawati Yaswir and Budi Mulyono} } @article {2306, title = {A Quasi-Experimental One Group Pre-Post Test Design in Air Traffic Controller in Indonesia: Progressive Muscle Relaxation}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {June 2024}, pages = {638-643}, type = {Research Article}, chapter = {638}, abstract = {

Objectives: The effectiveness of progressive muscle relaxation (PMR) in assessing the general health of air traffic controllers (ATC) is still insufficient, specifically when examining the psychological conditions of workers who use questionnaire instruments. Therefore, this research aimed to evaluate the use of PMR program in ATC by developing a model using biomarkers (saliva) tested on the cocorometer stress diagnostic tool and validity, including observing related determinants in the work environment. Methods: A quasi-experimental method was used, focusing on one group pre-post-test design for 92 respondents across six research areas in Indonesia. All respondents had received training in PMR methods conducted by psychologists. Subsequently, ongoing assistance was provided in implementing relaxation by a trained reminder team for eight weeks to maintain the precision and effectiveness of the intervention. Further analysis was conducted using the Wilcoxon signed rank test to evaluate the success of the intervention. Results: The implementation of PMR program in ATC reduced the incidence of stress levels after the observation. Statistically, the feeling of fatigue was a significant variable that decreased in mean value after the implementation of the relaxation program on the data review. The main benefit of PMR program in improving psychological health conditions (stress) was found in Surabaya branch ATC. Conclusions: The relaxation program was proven to reduce stress levels in ATC, showing an improvement in conditions before and after the implementation of PMR.

}, doi = {10.5530/pj.2024.16.100}, author = {Lalu Muhammad Saleh and Syamsiar S. Russeng and Istiana Tadjuddin and Iva Hardi Yanti and Nurul Mawaddah Syafitri and Yulianah Rahmadani and Mahfuddin Yusbud and Anwar Mallongi} } @article {2401, title = {Testing the Effectiveness of Anti-Aging Cream Preparations with Snakefish Extract (Channa Striata)}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {October 2024}, pages = {1164-1169}, type = {Research Article}, chapter = {1164}, abstract = {

Background: Skin aging is caused by dry, rough, scaly, less elastic skin with wrinkles and fold lines. Snakehead fish extract has high antioxidant activity so it can be used as an active ingredient in antiaging cosmetics. Objective: The aim of this research was to see the effectiveness of snakehead fish extract cream as an anti-aging agent. Methods: This research method includes formulating snakehead fish extract cream preparations with various concentrations including: 2.5\% (F1), 5\% (F2), 7.5\% (F3), 10\% (F4), evaluating the physical preparations in the form of: organoleptic test, homogeneity test, pH test, stability test, irritation test on volunteer skin, and anti-aging effectiveness test on volunteer skin for 4 weeks with 3 parameter tests, namely water content, pores and wrinkles. Results: The results of the study showed that there were changes that occurred in the volunteers as seen in the measurements of water content, pores and wrinkles on the volunteers{\textquoteright} faces. A good increase in changes was found in the F4 formula (10\%) in the wrinkle parameter test, namely 26.80\%. The number of wrinkles in volunteers from some wrinkles to few wrinkles. The conclusion of this research shows that snakehead fish extract ( Channa striata ) can be formulated in the form of a homogeneous cream dosage with a pH of 5.8 {\textendash} 6.7, and is stable when stored for 12 weeks at room temperature and does not cause skin irritation. Conclusions: There are differences in the results of each concentration of snakehead fish extract cream in influencing anti-aging effectiveness. The best concentration of 10\% snakehead fish extract showed better results compared to other creams in reducing the number of wrinkles on volunteers{\textquoteright} facial skin.

}, keywords = {Anti-Aging Cream, Formula, Snakehead Fish Extract}, doi = {10.5530/pj.2024.16.190}, author = {Cory Linda Futri Harahap and Hakim Soleh Harahap and Susi Yanti and Elmi Sariani and Anto J. Hadi and Nefonavratilova Ritonga and Haslinah Ahmad and Hapiz Arlanda Sani and Anwar Mallongi} } @article {2259, title = {An Ulcerative Cutaneous Plasmacytosis of the Scalp}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {April 2024}, pages = {378-381}, type = {Research Article}, chapter = {378}, abstract = {

Introduction: Cutaneous plasmacytosis (CP) is a rare benign disorder characterized by polyclonal proliferation of plasma cells of unknown etiology, with potential for malignant transformation. Clinical manifestations include reddish-brown macules, papules, plaques, or nodules, and, infrequently, ulcerative lesions resembling cutaneous squamous cell carcinoma (SCC) or similar cutaneous neoplasms. Case: Herein we reported a case of ulcerative CP which was initially suspected as SCC in a 77{\textendash}year{\textendash}old male. Physical examination revealed an ulcer with well{\textendash}defined borders, and flat edges, with a granulation tissue base on the scalp which was suggested as SCC. Histopathological features showed infiltration of mature plasma cells in the perivascular area, polyclonal plasma cell population on kappa and lambda chain immunohistochemistry, and hypergammaglobulinemia on protein electrophoresis that supported the diagnosis of CP. Discussion: Cutaneous plasmacytosis requires a comprehensive diagnostic evaluation, which typically includes clinical examination, histopathological analysis, immunohistochemistry, ancillary tests such as protein electrophoresis, and negative results from a diagnostic workup for systemic disease. Conclusion: The complexity of CP manifestations necessitates a rigorous diagnostic approach, enabling the differentiation of this benign condition from malignancies with similar presentations.

}, keywords = {Cutaneous plasmacytosis, Hypergammaglobulinemia, Plasma cell}, doi = {10.5530/pj.2024.16.58}, author = {Eva Krishna Sutedja and Eva Yustiana and Yogi Faldian and Hermin Aminah Usman} } @article {2091, title = {Community Empowerment with Independent Larva Monitor in Reducing the Dengue Hemorrhagic Fever Incidence, in Sidrap Regency}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {622-625}, type = {Research Article}, chapter = {622}, abstract = {

Objective: This study aims to determine the effectiveness of developing a community empowerment model through independent larva monitor with an overlap in controlling dengue disease incidence in Sidrap Regency. Methods: This study used a mix-method conducted in Tanete Village. The number of samples for quantitative data was 70 respondents, and the qualitative data was 12 informants. Data collection was carried out through Focus Group Discussions, observations, and interviews. The data were analyzed using the McNemar test. Results: The results showed that the behavior of the people affected by dengue fever is people who do not maintain the cleanliness of their environment, litter, and people{\textquoteright}s habits do not routinely drain water tanks, and drinking places for livestock become mosquito shelters. The results of dengue counseling showed a significant difference between people{\textquoteright}s behavior related to dengue fever disease before and after counseling. Most people stated that explanations related to how to make and the process of making ovitrap were easy to do. They were interested in making their own because they used materials that were easy to find at home. In addition, the community has been obedient in implementing independent romantic programs. The results of overlap observations show that simple overlap can trap mosquitoes. Conclusion: The development of empowerment models through independent larva monitor can be used to prevent and control dengue disease.

}, keywords = {Community Empowerment, Dengue fever, Independent Larva Monitor, Ovitrap}, doi = {10.5530/pj.2023.15.129}, author = {A. Arsunan Arsin and Ridwan Amiruddin and Dian Saputra Marzuki and Rezki Elisafitri and Basir and Anwar Mallongi and Aisyah and Ahmad Yani} } @article {2108, title = {Decreased Expression of Endocrine Glands Vascular Endothelial Growth Factor (EG-VEGF) in Rat Endometrial After Stimulation with Recombinants FSH Can be Reduce Implantation Rates}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {707-713}, type = {Original Article}, chapter = {707}, abstract = {

Background: Decreased expression of EG-VEGF in human endometrium after administration of ovarian stimulators has been reported to adversely affect endometrial receptivity and low implantation rates. Objective: To determine the effect of recombinant FSH administration on EG-VEGF protein in the endometrium of rats taken in the secretory phase and how it relates to endometrial receptivity. Design: A total of 36 female wistar rats with normal estrous cycles were randomly assigned to the natural cycle group (NC) and two stimulation groups (SC) which were injected with recombinant FSH at 12.5 IU and 25 IU intraperitoneally. Uterine necropsy and blood collection were performed on day 1, day 2, and day 3 after hCG administration. A total of 3 female rats from each group were mated with male rats (two males and three females in one cage). A successful marriage is indicated by the presence of a vaginal plug the next day. The level of EG-VEGF protein expression was assessed by immunohistochemical technique and steroid hormone levels were measured by the Elisa technique. Results: ANOVA test, that the expression of EG-VEGF in the endometrial glands showed a significant decrease from the normal cycle group to the stimulated cycle group 1 (SC 1) and SC2 (P = 0.00), as well as the expression of EG-VEGF in the endometrial stroma. (P = 000). Steroid hormone levels did not show a significant decrease between the normal cycle group and the stimulated cycle group (P = 0.48 and P = 0.13). Conclusion: Decreased EG-VEGF expression in rat endometrium after administration of recombinant FSH is associated with decreased endometrial receptivity which can reduce pregnancy rates.

}, keywords = {EG-VEGF, Endometrial receptivity, rFSH, Secretory phase.}, doi = {10.5530/pj.2023.15.141}, author = {Raden Muharam and Nurhuda Sahar and Kusmardi Kusmardi and Luluk Yunaini and Risqa Novita and Rosalina Thuffi and Conny Riana Tjampakasari and Ponco Birowo and Diyah Kristanty} } @article {2041, title = {Description of Ciplukan Toxicity (Physalis angulata L.)}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {June 2023}, pages = {357-367}, type = {Research Article}, chapter = {357}, abstract = {

Introduction: Ciplukan (Physalis angulata L.) is a plant used by Indonesian people as traditional medicine. Drug sanitization needs to be carried out to guarantee the use and availability of scientifically safe traditional medicines. This study aims to provide information and enrich knowledge about the safety of consuming ciplukan roots and stems. Methods: This study used 8 male mice as test animals, divided randomly into 4 treatment groups, namely mice treated with a dose of 0.56 mg/20 g body weight; mice treated with a dose of 5.6 mg/20 g body weight; mice treated with 56 mg/20 g body weight; and mice treated with 560 mg/20 g body weight. Treatment was given once and then observed for 24 hours to observe the number of deaths of the test animals. Then follow-up observations were carried out in 3 days on individuals who were still alive. Results: Within 24 hours all individuals at the treatment dose of 0.56 mg/20 g body weight survived, whereas all individuals at the treatment dose of 5.6; 56; and 560 mg/20 g body weight died. The observations on individuals treated at a dose of 0.56 mg/20 g body weight showed that the animals were in good condition, with sleeping and eating activities, moving a lot, having clean and nice fur, and not showing toxic symptoms such as disturbances in physical activity, impaired balance, and refusal to eat. Conclusions: The administration of the test extract below is less or equal to 0.56 mg/20 g body weight is relatively safe.

}, keywords = {Acute toxicity, Ciplukan, Condition, Dosage, Traditional medicine.}, doi = {10.5530/pj.2023.15.85}, author = {Ruqiah Ganda Putri Panjaitan and Titin and Yohanes Gatot Sutapa Yuliana} } @article {2074, title = {Diversity of Types of Medicinal Plants and Local Wisdom of the Kaili Tribe in Processing Medicinal Plants Around the Forest Areas of Central Sulawesi, Indonesia}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {535-540}, type = {Original Article }, chapter = {535}, abstract = {

The forest area in Sigi Regency, Central Sulawesi, is a habitat for various medicinal plant species. Forest areas must be managed appropriately for the local community and society{\textquoteright}s welfare and sustainable use. One of the local people living around the forest is the Kaili tribe. The local wisdom of the Kaili tribe, who inhabit forest areas in Central Sulawesi, in managing forests and forest products, especially using plants as medicine, must be documented in research. This study aimed to identify the species, habitat, habitus, and ways of using the plant as medicine by the Kaili people in the Sigi Regency. Prior to data collection, a literature study was conducted to obtain information regarding the condition of the research location around the forest area and the ethnic/ethnic groups who live permanently around and within the forest area. This stage was then followed by interviews and field surveys. The interviews were conducted by combining purposive sampling and snowball methods. The results showed the high potency of medicinal plants around forest areas used by the Kaili tribe, with the discovery of 113 species in 51 families. Herbs are the most common habitus of medicinal plants. The habitat of medicinal plants is mainly found in the yard. The most used plant part is the leaves, which can be boiled in water and drunk directly.

}, keywords = {Kaili tribe, Local knowledge, Medicinal plants, Species diversity.}, doi = {10.5530/pj.2023.15.115}, author = {Abdul Hapid and Ariyanti Ariyanti and Erniwati Erniwati and Ni Made Dharma Shantini Suena and Ketut Agus Adrianta and Karnita Yuniarti and Muthmainnah Muthmainnah} } @article {1994, title = {The Effect of Sapodilla Leaf Extract (Manilkara zapota L.) on Lipid Profiles of Alloxan-Induced Diabetic Mice}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {April 2023}, pages = {286-289}, type = {Original Article }, chapter = {286}, abstract = {

The aim of this study is to examine the effect of sapodilla leaf extract on lipid profiles of alloxan-induced diabetic mice. This research method are 30 male mice were used as experimental animals, which were randomly divided into five groups, each group consisting of 6 mice. The division of the group is as follows: Treatment of non-diabetic mice, diabetic mice, diabetic mice by administering pioglitazone at a dose of 2 mg/kg BW, extracts of manila sapodilla leaf (M. zapota L.) dose 100 mg/kg BW and 300 mg/kg BW. Observations were made on the 14th day, after administration of sapodilla leaf extract, mice were given light anesthesia and serum lipid profiles Total Cholesterol (TC), triglycerides (TG), High-Density Lipoprotein (HDL), and Low-Density Lipoprotein (LDL) were measured using diagnostic kits (Pars Azmoon Kit) and automatic analyzer (Abbot, model Alcyon 300). The results of this study are in TC, there was a significant difference in pioglitazone and 100 mg leaf extract against all treatment groups. In TG, there was a significant difference in pioglitazone and 300 mg leaf extract against all treatment groups. In LDL, there were significant differences in the 100 mg, 300 mg leaf extract and pioglitazone, against negative control, and diabetes control. In HDL, there was a significant difference in negative control and 300 mg leaf extract, against 100 mg leaf extract, pioglitazone, and diabetes control. The conclusions of this study exhibited the ethanol extract of M. zapota leaves contains several phytochemical compounds including alkaloids, flavonoids, saponins, polyphenols, tannins, quinones, and steroids. M. zapota leaves extract (100 mg/kg and 300 mg/kg) exhibited a significant effect on improvement in lipid protein.

}, keywords = {Alloxan, Diabetes, Lipid Protein, Manilkara zapota}, doi = {10.5530/pj.2023.15.40}, author = {Tridiganita Intan Solikhah and Tania Anggreani Wijaya and Salsabila and Daffa Alice Pavita and Ragil Kusnandar Miftakhurrozaq and Hartanto Mulyo Raharjo and Maya Nurwartanti Yunita and Faisal Fikri} } @article {2034, title = {Effect of Single-Bulb Garlic (Allium sativum Var. Solo Garlic) Extract on The Hematological Profile In E-Cigarette-Induced Male Sprague Dawley Rats}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {June 2023}, pages = {296-300}, type = {Original Article }, chapter = {296}, abstract = {

Garlic and its derivative preparations have long been used in traditional medicine for good health. Garlic is known to act as an antioxidant, antitumor, antibacterial, and antifungal. The antioxidant compound in singlebulb garlic is considered to be better than the antioxidant content in other species of garlic. This research aimed to study the effect of hematological profile in oral administration of single-bulb garlic extract in e-cigarette-induced male Sprague Dawley rats. The method used in this study was randomized post-test only control group design. Twenty-four rats were randomly distributed into six groups. The group consisted of C (-) as normal rats{\textquoteright} control; C (+) only exposed to e-cigarette smoke; T1 exposed to e-cigarette smoke and treated with vitamin C; T2 exposed to e-cigarette and treated with single-bulb garlic extract 75 mg/kg BW; T3 exposed to e-cigarette and treated with single-bulb garlic extract 100 mg/kg BW; and T4 exposed to e-cigarette and treated with single-bulb garlic extract 125 mg/kg BW. Exposure to e-cigarette smoke is conducted by evaporating the liquid into a gas chamber with a nicotine dose of 3.6 mg/ml. All treatments were given for 14 days. On the 15th day, the rats were sacrificed. Blood samples were collected by the cardiac puncture method and were examined using a hematology analyzer. Data obtained were white blood count (WBC), platelets, hemoglobin, hematocrit, and erythrocytes that were analyzed with one-way ANOVA. The result of this study is that garlic extract may boost immunity in the body. However, higher doses can be toxic to erythrocytes.

}, keywords = {Antioxidant, E-cigarette, Good health, Hematology profile}, doi = {10.5530/pj.2023.15.78}, author = {Maya Nurwartanti Yunita and Julia Calvina Fauzi and Zahra Defitra Rahmania and Bella Safinda and Tridiganita Intan Sholikhah and Bodhi Agustono and M. Gandul Atik Yuliani and Shekhar Chhetri and Reina Puspita Rahmaniar} } @article {2029, title = {The Effect Supplementation of Microbiota Inoculant in the Early Laying Hens Feed on High Density Lipoprotein (HDL) and Low- Density Lipoprotein (LDL) in Egg Yolk}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {June 2023}, pages = {270-273}, type = {Original Article }, chapter = {270}, abstract = {

Laying hens (Gallus gallus) are one of the poultries kept for their eggs. Eggs produced by chickens are used as a source of human food that contains a lot of nutrition and is affordable. Eggs also contain high levels of cholesterol in the yolk, so if consumed in large quantities, they will pose a risk of disease. This study aims to determine the effect of giving probiotics in the early layer laying hen feed on the levels of high-density lipoprotein and low-density lipoprotein in egg yolks. This study has four treatments, namely P1 = control, P2 = feed + AGP, and P3 and P4 = feed + probiotics. The probiotic used is a combination of three bacteria, namely Lactobacillus plantarum, Lactobacillus acidophilus, and Bifidobacterium sp. The sample used in this study was egg yolk, which was collected in the last week of the study. Testing for HDL and LDL levels in egg yolks was carried out using the Quantitative Colorimetric/Fluorometric Determination of HDL and LDL/VLDL method. Testing HDL and LDL levels in this study showed that the administration of probiotics had an effect in the form of increasing HDL levels but did not have an effect in the form of a significant decrease in egg yolk LDL levels during the four-week treatment period in laying hens in the early layer phase, aged 18{\textendash}22 weeks. The best probiotic dose used among the three probiotic doses is 3 ml/kg of feed.

}, keywords = {High Density Lipoprotein, Laying hens, Low Density Lipoprotein, Probiotics.}, doi = {10.5530/pj.2023.15.73}, author = {Bodhi Agustono and Rini Apriliawati and Sunaryo Hadi Warsito and Maya Nurwartanti Yunita and Widya Paramita Lokapirnasari and Sri Hidanah and Emy Koestanti Sabdoningrum and Mohammad Anam Al-Arif and Mirni Lamid and Gandul Atik Yuliani and Shekhar Chhetri and Sarasati Windria} } @article {2171, title = {Extract of Torbangun (Coleus amboinicus Lour) Leaves Inhibits the Expression of PEPCK and G6Pase in Streptozotocin-Induced Diabetic Rats}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1116-1120}, type = {Research Article}, chapter = {1116}, abstract = {

Objective: This study aimed to analyze the anti-hyperglycemic activity of Torbangun leaf extract (TLE) in hyperglycemic rats by observing its effect on blood glucose levels and PEPCK and G6Pase gene expression. Method: This post-test-controlled group design study used a completely randomized design (CRD). Seven rats were separated as a normal group (N) and other rats were injected with streptozotocin (STZ). Hyperglycemia was characterized by fasting blood glucose (FBG) \>126 mg/dl. Hyperglycemic rats were divided into three groups: H-IM (control drug metformin hydrochloride dose 62.5 mg/kg BW), H-IT (TLE dose 620mg/kg BB), and NG (negative control, hyperglycemic rats). Rats were given intervention for 14 days. Result: The results showed a significant difference between initial and final FBG of the HI-IM group (p = 0.002, α = 0.01) and the H-IT group (p = 0.005, α = 0.01) and effect on the key gene expression of gluconeogenesis in the liver. The H-IT group showed a decrease in PEPCK gene expression 0.80 times and decreased G6Pase gene expression by 0.65 times compared to NG group. Conclusion: The findings suggested the administration of TLE in STZ-induced hyperglycemic rats was able to reduce blood sugar levels and was involved in inhibiting the expression of PEPCK and G6Pase expression genes in the liver.

}, keywords = {G6Pase, hyperglycemia, PEPCK, Rats, Torbangun}, doi = {10.5530/pj.2023.15.203}, author = {Meilla Dwi Andrestian and Rizal Damanik and Faisal Anwar and Nancy Dewi Yuliana and Anwar Mallongi} } @article {2105, title = {Hepatitis E Inhibited by Rosmarinic Acid Extract from Clove Plant (Syzygium Aromaricum) through Computational Analysis}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {518-523}, type = {Original Article }, chapter = {518}, abstract = {

This study aims to evaluate the potential of Rosmarinic Acid as an inhibitor against Hepatitis E by interacting with the active site of the Tyrosine FYN protein. Computational approaches were employed to predict the molecular interactions between Rosmarinic Acid and Tyrosine FYN. The research methodology involved the use of software such as Pymol, Pyrex, Protein Plus, and the Lepinski Rule. Docking analysis was conducted using Pymol to obtain information about the binding energy between Rosmarinic Acid and Tyrosine FYN. The results of the analysis showed that Rosmarinic Acid exhibited a Binding Affinity of -8.3, -8, and -7.9, indicating a strong affinity towards the target protein. Additionally, Root Mean Square Deviation (RMSD) values of 0, 15.905, and 17.014 were used to assess the stability of the formed protein-ligand complex. Analysis using Protein Plus revealed interactions between Rosmarinic Acid and Tyrosine FYN. Furthermore, analysis using the Lepinski Rule to examine the physicochemical properties of Rosmarinic Acid indicated that the molecule had a mass of 360, 5 hydrogen bond donors, 8 hydrogen bond acceptors, a log P value of 1.76, and a molar reactivity of 89.8. These findings highlight the potential of Rosmarinic Acid as an inhibitor of Hepatitis E through its interaction with the Tyrosine FYN protein, providing a basis for the development of potential new therapies in the treatment of this disease.

}, keywords = {Hepatitis E, Molecular Docking., Rosmarinic acid, Syzygium aromaricum, Tyrosine FYN}, doi = {10.5530/pj.2023.15.112}, author = {Sunadi and Saddam Al Aziz and Fadhilah Fitri and Devni Prima Sari and Muhammad Raffi Ghifari and Rismi Verawati and Nita Yessirita and Oski Illiandri and Riso Sari Mandeli and Devi Purnamasari and Putri Azhari and Rahadian Zainul and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2104, title = {In Silico Study of Rhamnocitrin Extract from Clove Syzygium Aromaricum in Inhibiting Adenosine A1 Adenylate Cyclase Interaction}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {512-517}, type = {Original Article }, chapter = {512}, abstract = {

This study aims to analyze the potential of Rhamnocitrin, a compound found in clove extract (Syzygium aromaticum), as an inhibitor of Adenylate Cyclase through an in-silico approach. The research method involves the use of software such as Pymol, PyRx, Protein Plus, and Lipinski Rule for molecular interaction analysis and physicochemical characterization of Rhamnocitrin. The analysis results show that Rhamnocitrin has significant affinity towards Adenosine A1 with Binding Affinity values of -6.1, -5.8, and -5.7. RMSD analysis indicates good stability of the formed protein-ligand complexes, with RMSD values of 0, 3.129, and 3.696. Analysis using Protein Plus software reveals the interaction between Rhamnocitrin and Adenosine A1, while the lipinski analysis shows physicochemical characteristics of Rhamnocitrin that meet important criteria, such as a mass of 300, 3 hydrogen bond donors, 6 hydrogen bond acceptors, log P of 2.6, and molar reactivity of 77.27. These findings provide new insights into the development of potential therapies involving clove extract and Rhamnocitrin as inhibitors of Adenylate Cyclase, and further research is needed to validate their effectiveness and safety.

}, keywords = {Adenosine A1, Adenylate Cyclase inhibition, Molecular Docking., Rhamnocitrin, Syzygium aromaricum}, doi = {10.5530/pj.2023.15.111}, author = {Nita Yessirita and Rismi Verawati and Devi Purnamasari and Rollando Rollando and Riso Sari Mandeli and Muhammad Thoriq Albari and Putri Azhari and Rahadian Zainul and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2063, title = {Interaction of Masilinic Acid from Clove Plant (Syzygium aromaticum) with CD81 Antigen in Inhibiting HIV Virus Regulation In Silico}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {484-488}, type = {Original Article }, chapter = {484}, abstract = {

This research explores the interaction of Masilinic Acid from the clove plant (Syzygium aromaticum) with the CD81 antigen to inhibit HIV virus regulation in silico. Using computational methods such as Pymol, Pyrex, and Protein Plus, we demonstrate that Masilinic Acid can significantly interact with the CD81 antigen. The obtained data shows binding affinities of -6.4, -6.2, and -5.7, and RMSD values of 0, 1.885, and 1.952. Further detailed interaction analysis with Protein Plus strengthens these findings, providing evidence of a strong interaction between Masilinic Acid and the CD81 antigen. This study also includes the testing of the Lepinski Rule of Five to assess the potential of Masilinic Acid as a drug candidate, with results indicating a mass of 472, three hydrogen bond donors, four hydrogen bond acceptors, a log P value of 6.2, and a molar reactivity of 134. These results indicate that Masilinic Acid has the potential as an inhibitor of the CD81-HIV interaction, which can be utilized as an effective antiviral strategy. Key words: Masilinic Acid, Clove plant, CD81 antigen, HIV virus, In silico.

}, keywords = {CD81 antigen, Clove plant, HIV virus, In Silico., Masilinic Acid}, doi = {10.5530/pj.2023.15.106}, author = {Rahadian Zainul and Elsa Yanuarti and Siti Amiroch and Muhammad Thoriq Albari and Rismi Verawati and Amalia Putri Lubis and AAA Murtadlo} } @article {2155, title = {Qualitative Study on Adolescent Marriage and The Risk of Stunting in South Kalimantan}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1016-1023}, type = {Original Article}, chapter = {1016}, abstract = {

Objective: An exploratory qualitative investigation to determine the causes of adolescent marriage, analyze the effect of early marriage on stunting, and analyze the food patterns of toddlers in adolescent marriage in South Kalimantan, Indonesia. Method: The method used is phenomenology using the FGD system and in-depth interviews. Participants include the FGD informants from the Family Planning Regional Apparatus Organization, the Office of Women{\textquoteright}s Empowerment and Child Protection and the Office of Religious Affairs from 13 Regencies/ Cities in South Kalimantan. In-depth interview informants were adolescent marriage offenders and their parents, adolescent pregnant women, midwives, integrated health service post cadres, and community leaders each taken from three Regencies/ Cities. Results: There are not many formal adolescent marriages because they have to get a recommendation from the Religious Courts. Adolescent marriages mostly occur through informal marriages. The high rate of early marriage in South Kalimantan Province is caused by culture and weak enforcement of the rules. The incidence of adolescent marriage is caused by promiscuity and information. Meanwhile, adolescent marriage is mostly due to economic motives and limited education facilities in rural areas. Adolescent marriage is not closely related to the incidence of stunting, but low education can be a factor in the inability of parents to provide good parenting, especially feeding pratice. Conclusions: Adolescent marriages appear to be triggered by economic motives and teenagers{\textquoteright} desires, as well as driven by economic conditions, social influences, and a lack of encouragement to complete formal education. It was observed that stunting is more common among toddlers with adolescent mothers than toddlers with adult mothers. There is a poor feeding parenting pattern of toddlers with adolescent parents.

}, keywords = {Adolescent marriage, Qualitative investigation, Stunting, Toddler feeding pattern}, doi = {10.5530/pj.2023.15.187}, author = {Meilla Dwi Andrestian and Meitria Syahadatina Noor and Resa Ana Dina and Ayunina Rizky Ferdina and Zulfiana Dewi and Niken Widyastuti Hariati and Purnawati Hustina Rachman and Muhammad Irwan Setiawan and Windy Tri Yuana and Ali Khomsan} } @article {1971, title = {Sun Protection Factor Activity of Jamblang Leaves Serum Extract (Syzygium cumini)}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {March 2023}, pages = {134-140}, type = {Research Article}, chapter = {134}, abstract = {

Background: The development of serum preparations containing natural ingredients for sun protection is growing rapidly. Jamblang (Syzygium cumini) leaves are rich in phenolic compounds that can inhibit free radicals causing premature aging. Therefore, this study aims to determine the potential of S. cumini serum extract as sun protection. Methods: The extract was prepared and included in the serum base. The formulations were evaluated for rheological, pH, dispersion coefficient, and stability examinations. Furthermore, Sun Protection Factor was tested using a UV-Vis spectrophotometer. Results: The test of phytochemical compounds showed the presence of alkaloids, flavonoids, polyphenols, tannins, saponins, quinones, monoterpenoids, sesquiterpenoids, triterpenoids, and steroids. The result also showed that all serum formulations met the predetermined requirements. Furthermore, the extract has protective activity against ultraviolet rays, which was indicated by the SPF value. The higher the dose of S. cumini extracts in the serum formulation, the higher the value obtained. Formulations 1, 2, and 3 have SPF of 9.35{\textpm}0.11, 13.26{\textpm}0.16, and 26.05{\textpm}0.31, respectively. This indicates that they all met the Indonesian National Standard, that a sun protection preparation must have a minimum protection factor of 4. Conclusion: S. cumini extract serum has the potential to be developed as a new sun protection agent against ultraviolet radiation. However, further studies are still needed to determine the mechanism of its constituent active compounds.

}, keywords = {Serum, Sun protection factor, Syzygium cumini, Ultraviolet.}, doi = {10.5530/pj.2023.15.18}, author = {Himyatul Hidayah and Surya Amal and Nia Yuniarsih and Farhamzah and Anggun Hari Kusumawati and Neni Sri Gunarti and Ermi Abriyani and Iin Lidia Putama Mursal and Adinda Khansa Sundara and Maulana Yusuf Alkandahri} } @article {1880, title = {Analysis Protein APOB and TroponinT in Obese Mice (Musmusculus) Induced by Static Magnetic Field as a Marker of Coronary Heart}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {627-631}, type = {Research Article}, chapter = {627}, abstract = {

Obesity is closely related to cardiovascular disease. APOB protein was a better predictor of LDL particle count. Increased troponin T protein is also indicated as an indication of the risk of CHD disease. Static Magnetic Field (SMF) is an electromagnetic applied in therapy because only a simple magnetic disk is used to generate it both in vitro and in vivo. The use of SMF is considered to affect the biological state of cells so that it can affect weight loss in mice. The method used was male c57bl/6j mice with groups of Obes0, Obes2, Obes7, Obes 14, and Obes21 fed high-fat diet and then exposed to SMF with an intensity of 2mT for 1 hour. The results obtained were that there was a significant difference p=0.015 (p\<0.05) in the protein concentration of APOB and there was no significant difference in the concentration of cTnT taken from the blood serum of mice. The increase in APOB protein levels in each control group was not found to have an increase in cTnT protein so that the two proteins did not have a linear correlation between the two proteins 0.598 (p\>0.05). Most of the protein concentrations of APOB and cTnT decreased in concentration at longer days. It can be seen morphologically in the heart there is a decrease in the number of adipose cells.

}, keywords = {Cardiovaskular, Electromagnetic, Obesity, Protein.}, doi = {10.5530/pj.2022.14.145}, author = {Puji Sari and Luluk Yunaini and Dwi Anita Suryandari and Widia Bela Oktaviani and Rahma Nur Istiqomah and Umiatin} } @article {1758, title = {Antimalaria Activities of Several Active Compounds from Medicinal Plants}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {February 2022}, pages = {245-252}, type = { Review Article}, chapter = {245}, abstract = {

The growth and spread of resistance to all first-line antimalarial drugs used in the treatment of malaria today has caused many problems in eradicating malaria in various countries in the world. Researchers have begun to look for candidates for new antimalarial drug compounds derived from natural products that have been scientifically proven to have antimalarial activity. This is done to replace antimalarial drugs that are currently experiencing resistance. Some active compounds that have been successfully isolated from various plants, including curcumin, kaempferol, piperine, andrographolide, α-mangostin, catechin, luteolin and betulinic acid, have been scientifically tested to have antimalarial activity with different mechanisms of action.

Key words: Malaria, Antimalarial, Curcumin, Kaempferol, Piperine, Andrographolide, α-Mangostin, Catechin, Luteolin, Betulinic acid.

}, doi = {10.5530/pj.2022.14.30}, author = {Maulana Yusuf Alkandahri and Nia Yuniarsih and Afiat Berbudi and Anas Subarnas} } @article {1913, title = {Correlation of the Presence of Non Structural-1 (NS1) Antigen Dengue Virus with Severity of Dengue Infection}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {813-816}, type = {Research Article }, chapter = {813}, abstract = {

Dengue is a major public health threat worldwide, affecting approximately 3 billion people. More than 100 countries in the world located in tropical and subtropical areas, there are at least 100 to 400 million people infected with the dengue virus which causes dengue hemorrhagic fever (DHF). Soluble Non Structural Protein (sNS1) DENV is a soluble NS1 protein that is secreted and found in the serum of patients during acute infection. Because of its presence early in infection, sNS1 is used as a diagnostic indicator of acute dengue infection. NS1 can directly activate platelets through TLR4 and can further increase platelet aggregation, endothelial cell adhesion, and phagocytosis by macrophages that can cause thrombocytopenia so that high sNS1 levels are associated with disease severity. From the results of the study showed p \<0.05. This indicates that there is a correlation between the presence of NS1 and the severity of dengue infection.

}, keywords = {Dengue virus, NS1 antigen, Thrombocytopenia}, doi = {10.5530/pj.2022.14.172}, author = {Ichwan Baihaki and Beti Ernawati Dewi and Viol Dhea Kharisma and Ahmad Affan Ali Murtadlo and Muhammad Badrut Tamam and Devi Purnamasari and Nunuk Hariani Soekamto and ANM Ansori and Kuswati and Riso Sari Mandeli and Kawther Ameen Muhammed Saeed Aledresi and Nur Farhana Mohd Yusof and Vikash Jakhmola and Maksim Rebezov and Pavel Burkov and Marina Derkho and Pavel Scherbakov and Rahadian Zainul and Muhammad Raffi Ghifari and Asmi Citra Malina AR Tasakka and Tengku Siti Hajar Haryuna} } @article {1827, title = {Description of Acute Toxicity of Ketepeng Root Extract (Senna alata (L.) Roxb.)}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {August 2022}, pages = {393-401}, type = {Research Article}, chapter = {393}, abstract = {

Introduction: People in Indonesia, especially in the West Kalimantan region often use the root of ketepeng as a medicine to treat jaundice, but they lack knowledge regarding the appropriate dosage. Therefore, this study aims to determine the acute toxicity of ketepeng root extract. Methods: The sample population consists of 8 male mice, which were randomly divided into 4 treatment groups, namely P1, P2, P3, and P4 with dosages of 0.56 mg, 5.6 mg, 56 mg, and 560 mg/20 g body weight, respectively. The extract was administered once, after which the samples were observed for 24 hours to record the number of deaths. Follow-up observations were then carried out for 3 days on the mice that survived the test. Results: The results showed that within 24 hours of administration, the samples in P1 were alive, while all animals in the other groups died. Furthermore, the follow-up observations on animals that survived showed that they were in good condition with no toxic symptoms, such as balance disorders, refusal to eat, and lack of physical activity. Conclusion: Based on the results, the administration of 0.56 mg/20 g body weight of the extract was relatively safe, while higher doses can cause death. However, further testing must be carried out to complete the toxicity information as well as to determine the exact dosage range to avoid mortality during the treatment.

}, keywords = {Acute toxicity, Fabaceae, Roots of Senna alata (L.) Roxb}, doi = {10.5530/pj.2022.14.113}, author = {Ruqiah Ganda Putri Panjaitan and Titin and Yohanes Gatot Sutapa Yuliana} } @article {1925, title = {Differences in interleukin-6 and interleukin-17 expression in covid-19 post-mortem lung tissue biopsy compared with noncovid- 19}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {January 2023}, pages = {887-892}, type = {Original Article }, chapter = {887}, abstract = {

Background: COVID-19 has spread rapidly around the world. It is necessary to study lung tissue of postmortem COVID19 patients to determine the molecular alteration particularly the role of IL-6 and IL-17 in causing fatality. Objective: This study aims to determine the differences in the expressions of IL-6 and IL-17 in lung tissue of post-mortem COVID-19 patients compared to non-COVID-19 patients. This study also aimed to analyze the correlation between the expressions of IL-6 and IL-17 in lung tissue of post-mortem COVID-19 patients. Methods: This research is an observational analytic study with crosssectional approach. The samples were 15 paraffin blocks of post-mortem lung tissue biopsy of COVID-19 patients, and 15 paraffin blocks of inflammatory lung tissue biopsy or surgery of non-COVID-19 patients. IL-6 and IL-17 expressions were evaluated by immunohistochemical procedure. Result: There was a significant difference in the expression of IL-6 in the COVID-19 group and the non-COVID-19 group with a p-value = 0.001 (p \< 0.05). There was a significant difference in the expression of IL-17 in the COVID-19 group and the non-COVID-19 group with p-value = 0.001 (p \< 0.05). There was a significant correlation between the expressions of IL-6 and IL-17 in the COVID-19 group, with the Spearman coefficient value (rs) of 0.548 with p = 0.034 (p \< 0.05). Conclusion: There are differences in the expression of IL-6 and IL-17 between COVID-19 and non-COVID-19 lung tissue. There is a significant correlation between the expressions of IL-6 and IL-17 in post-mortem lung tissue of COVID-19 patients.

}, keywords = {Biopsy, COVID-19, IL-17, IL-6, Post mortem lung tissue.}, doi = {10.5530/pj.2022.14.184}, author = {Etty Hary Kusumastuti and Priangga Adi Wiratama and Grace Ariani and Stephanie Natasha Djuanda and Alphania Rahniayu and Nila Kurniasari and Dyah Fauziah and Anny Setijo Rahaju and Isnin Anang Marhana and Alfian Nur Rosyid and Dwi Wahyu and Gilang Muhammad Setyo Nugroho and Adhitri Anggoro and I Komang Rusgi Yandi and Bambang Pujo Semedi and Jilientasia Godrace Lilihata and Ummi Maimunah and Supriadi and Achmad Lefi and Lalu Galih Pratama Rinjani and Edi Suyanto and Ricardo Ardian Nugraha} } @article {1834, title = {Effects of Golden Sea Cucumber Extract (Stichopus hermanni) on Hyphae, Neutrophils and TNF-α in BALB/c Mice Inoculated with C. albicans Intravaginally}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {August 2022}, pages = {278-285}, type = {Original Article }, chapter = {278}, abstract = {

Introduction: Candidal vaginitis is an inflammatory disease that caused mainly by Candida albicans. Yeast transitions to filamentous hyphae considered the most important virulence factor. Neutrophils are the first line of defense of the immune system, but in patients with Candidal vaginitis the recruitment of neutrophils into the vaginal lumen is positively correlated with symptoms of the disease. This is supported by the release of proinflammatory cytokines such as TNF-α. Standard treatment is considered less effective in relieving symptoms, so other alternative/adjunctive treatments are needed. Golden sea cucumber (Stichopus hermanni) extract has been widely studied, especially for anti-fungal and anti-inflammatory. This study aims to analyze the mechanism of decreasing number of hyphae and neutrophils, and proinflammatory cytokine TNF-α in BALB/c mice inoculated intravaginally with C. albicans after administration of golden sea cucumber extract (S. hermanni). Methods: Experimental research uses a post-test only control group design. The experimental unit consisted of 36 BALB/c mice that were inoculated intravaginally with C. albicans and divided into 4 groups, group that did not receive treatment (K-), group that received standard treatment fluconazole (K+), group that received treatment with golden sea cucumber extract (S. hermanni) (P1) and group that received standard treatment with fluconazole plus extract of golden sea cucumber (S. hermanni) (P2). The hyphae and neutrophils number were seen microscopically on vaginal mucosal tissue. Cytokine levels of TNF-α were seen from the ELISA blood samples. Results: Results showed from the vaginal mucosal tissue of mice, there was significant difference in the number of hyphae (p = 0.001) between groups and no significant difference in the number of neutrophils (p = 0.070) between groups. From the blood serum of mice, there were significant differences in TNF-α levels (p=0.001) between groups. From the path analysis obtained a significant relationship from the number of hyphae to the number of neutrophils (p = 0.034) and the number of neutrophils to TNF-α levels (p = 0.021). The strength of the pathway from number of hyphae to number of neutrophils (β= 0.354) and number of neutrophils to TNF-α levels (β= 0.382) with positive interactions all. Conclusion: In summary, the administration of S. hermanni extract was able to reduce the number of hyphae, neutrophils and TNF-α levels through the hyphae, neutrophil and TNF-α pathway.

}, keywords = {Candida vaginitis, Hyphae, Neutrophils, Stichopus hermanni extract, TNF-α}, doi = {10.5530/pj.2022.14.97}, author = {Varidianto Yudo and Widjiati and Harianto Notopuro and Yulianto Listiawan and Budi Utomo and Purwo Sri Rejeki and Prawesty Diah Utami and Aryati} } @article {1873, title = {In Silico Screening of Bioactive Compounds from Garcinia mangostana L. Against SARS-CoV-2 via Tetra Inhibitors}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {575-579}, type = {Research Article}, chapter = {575}, abstract = {

The global COVID-19 pandemic caused by SARS-CoV-2 has been the resulted of massive human deaths since early 2020. The purpose of this study was to determine the potential of mangosteen (Garcinia mangostana L.) as an inhibitor of RBD spike, helicase, Mpro, and RdRp activity of SARS-CoV-2 with an in silico approach. The samples were obtained from PubChem and RCSB PDB. Analysis of the similarity of the drug was carried out with the Swiss ADME on the basis of Lipinski rule of five. Prediction of antivirus probabilities was carried out using PASS Online. Molecular screening was performed using PyRx through molecular docking. Discovery Studio was used for visualization. The bioactive compounds with the highest antiviral potential were indicated with the lowest binding affinity to the targeted proteins RBD spike, helicase, Mpro, and RdRp of SARS-CoV-2. The results indicated that mangiferin has the greatest potential as a potential antiviral. However, more research is required to validate the results of these computational predictions.

}, keywords = {Antiviral agent, Garcinia mangostana L., in silico, SARS-CoV-2}, doi = {10.5530/pj.2022.14.138}, author = {Nur Sofiatul Aini and Viol Dhea Kharisma and Muhammad Hermawan Widyananda and Ahmad Affan Ali Murtadlo and Rasyadan Taufiq Probojati and Dora Dayu Rahma Turista and Muhammad Badrut Tamam and Vikash Jakhmola and Elsa Yuniarti and Saddam Al Aziz and Muhammad Raffi Ghifari and Muhammad Thoriq Albari and Riso Sari Mandeli and Muhammad Arya Ghifari and Devi Purnamasari and Budhi Oktavia and Amalia Putri Lubis and Fajriah Azra and Fadhilah Fitri and ANM Ansori and Maksim Rebezov and Rahadian Zainul} } @article {1741, title = {In Silico Studies of Sesquiterpene Lactones from Vernonia amygdalina Delile on the Expression of EGFR and VEGFR as a New Anticancer Potential}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {February 2022}, pages = {91-97}, type = {Original Article}, chapter = {91}, abstract = {

Objective: To assess the inhibition activity of sesquiterpene lactones from Vernonia amygdalina Delile as a new anticancer potential on the expression of cancer therapeutic target-proteins, namely: epidermal growth factor receptor (EGFR), and vascular endothelial growth factor receptor (VEGFR). Methods: The in silico screening, target-based approach (docking) was performed by the Prediction of Activity Spectra for Substances (PASS) website and AutoDock Vina program. The therapeutic cancer target proteins model of EGFR and VEGFR were downloaded from Research Collaboratory for Structural Bioinformatics (RCSB) protein data bank (PDB) with 5HG7 and 4AG8 as their respective codes. Results: The test compounds have anticancer activity as predicted by the Prediction of Activity Spectra for Substances (PASS) website and AutoDock Vina program. The molecular docking analysis of the test compounds showed strong interactions and good inhibition activity with the targeted proteins with a low docking score value predicted by the AutoDock Vina program. Conclusion: The test compounds have the potential to be used in anticancer drugs through the inhibitory qualities of EGFR and VEGFR.

Key words: In silico, Sesquiterpene lactones, EGFR, VEGFR, Vernonia amygdalina Delile.

}, doi = {10.5530/pj.2022.14.13}, author = {N Nerdy and P Lestari and F Fahdi and EDL Putra and SAB Amir and F Yusuf and TK Bakri} } @article {1912, title = {In Silico Study of the Potential of Endemic Sumatra Wild Turmeric Rhizomes (Curcuma Sumatrana: Zingiberaceae) As Anti-Cancer}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {806-812}, type = {Research Article }, chapter = {806}, abstract = {

Cancer is one of the diseases that is the highest cause of death in humans. Most human cancer cells are formed as a result of over-expression of anti-apoptotic proteins. Thus, the activation of these proteins can inhibit pro-apoptotic proteins, then apoptosis will be inhibited so that other apoptotic pathways need to be activated to prevent cancer cells from developing. Current cancer treatments, such as chemotherapy using synthetic compounds, have various side effects, so research on natural based therapies can be used as an alternative in cancer treatment. Curcuma sumatrana is one of the plants of the Zingiberaceae family which is an endemic plant from Sumatra which is found along the Bukit Barisan. The research was carried out in silico by analyzing the potential bioactivity of the compounds, testing the bioavailability, toxicity, and molecular docking of the bioactive compounds from the ethanol extract of the rhizome of C. sumatrana which had been previously identified through gas chromatography-mass spectroscopy (GCMS) analysis. The results obtained that the compound 9-Acetyl-S-octahydrophenanthrene and 3-Oxoandrosta- 1,4-dien-17.beta.-spiro-2{\textquoteright}-3{\textquoteright}-oxo-oxetanecontained in C. sumatrana has the potential to be developed as an anticancer where the compound has good bioavailability value and is not toxic and potentially can trigger apoptosis. However, the results of this study need to be analyzed further with an in vitro or in vivo approach.

}, keywords = {Anticancer, C. sumatrana, in silico}, doi = {10.5530/pj.2022.14.171}, author = {Aldi Tamara Rahman and Rafia and Aiken Jethro and Putra Santoso and Viol Dhea Kharisma and Ahmad Affan Ali Murtadlo and Devi Purnamasari and Nunuk Hariani Soekamto and ANM Ansori and Kuswati and Riso Sari Mandeli and Kawther Ameen Muhammed Saeed Aledresi and Nur Farhana Mohd Yusof and Vikash Jakhmola and Maksim Rebezov and Maksim Rebezov and Rahadian Zainul and Kiran Dobhal and Tarun Parashar and Muhammad Arya Ghifari and Deffi Ayu Puspito Sari} } @article {1939, title = {Job fulfilment and its related variables among pharmacy certificate holders in Jordan: A Cross-sectional Study}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {January 2023}, pages = {983-988}, type = {Research Article }, chapter = {983}, abstract = {

Background: The feeling of contentment one has with their job is referred to as job satisfaction. The quality of health care, processes, and services are directly impacted by pharmacists{\textquoteright} job satisfaction, which is a key factor in influencing their motivation. Nevertheless, there hasn{\textquoteright}t been much research done to evaluate the employment satisfaction of Jordanian pharmacists working in various professions and locations. This study assessed the job satisfaction level among all pharmacy certificate carriers (Doctor of pharmacy, pharmacists, clinical pharmacists, industrial pharmacists, academic pharmacists, and assistant pharmacists) in Jordan and the elements that influence their level of job satisfaction which finally affect their job performance and employee turnover. Methods: This cross-sectional inquiry comprised Jordanian pharmacy certificate holders. Online national surveys on job satisfaction were conducted using a reputable, well-designed questionnaire. The questionnaire has 22 criteria for measuring job satisfaction. Logic regression analyses were utilized in order to examine the relationship between sociodemographic variables, work satisfaction indicators, and overall job satisfaction levels. Results: The study received responses from 236 pharmacy certificate holders. The mean introducing age was middle age (30-39yrs) (52.6\%), with the majority being females (87.5\%). The overall job satisfaction level reported by participants had a mean score of 2.97, with 14.4\% of them being satisfied with their jobs. Salary and a lack of promotion opportunities were found to be significantly related to overall job satisfaction (p = 0.001, p=0.011 respectively). Conclusion: The majority of Jordanian pharmacy certificate holders were dissatisfied with their jobs. Increasing salary and advancement opportunities would increase job satisfaction among pharmacy certificate holders in the country. There is a need for effective human resource management and policy revision in the pharmacy sector in Jordan.

}, keywords = {Employee turnover., Job satisfaction, Pharmacy certificate holders}, doi = {10.5530/pj.2022.14.200}, author = {Noha Abd Alkareem Younis Younis} } @article {1869, title = {Pathophysiological Electrolyte Changes Connoted via Antagonism of Serotonin Receptor in Experimental Animals}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {548-552}, type = {Research Article}, chapter = {548}, abstract = {

Background: Atypical antipsychotics are a subclass of antipsychotics that have emerged primarily since the 1970s for the treatment of psychiatric disorders. They are sometimes referred to as second-generation antipsychotics (SGAs). Several atypical antipsychotics have received regulatory approval for the treatment of disorders such as bipolar disorder, schizophrenia, irritability in autism, and as adjunctive treatment for major depressive disorders. Objectives: The purpose of the following study was to evaluate the effect of two widely known atypical antipsychotics, aripiprazole, and risperidone, on pathophysiological fluctuations in electrolytes. Several other studies were based on the following ideas, which brought a variety of different perspectives. As can be seen in the following evaluation, although atypical antipsychotics reduce the chance of extrapyramidal symptoms, it leads to impairment of renal function and destruction of renal histo-morphology. Materials and Methods: Thirty rats (10 per group) were used for this study, control group received normal saline, aripiprazole group received 10mg/kg//day, and risperidone group received 20mg/kg//day. The duration of therapy was long up to 3 months. Results: the results confirmed that both drugs reduced plasma sodium and chloride concentration with no effects on plasma potassium and calcium concentration. Moreover, the histomorphology at microscopic level shown no defects after 3 months of therapy. Conclusion: the outcome confirmed no deleterious defects associated with aripiprazole and risperidone when used for 3 months.

}, keywords = {Aripiprazole, Calcium, Chloride, Electrolyte, Potassium, Risperidone, Sodium}, doi = {10.5530/pj.2022.14.134}, author = {Mohammed D Mahmood and Mohammed A. Younes and Mohammed Saarti} } @article {1791, title = {Phytochemical Evaluation and Antioxidant Activity of Virginia tobacco Leaves (Nicotiana tabacum L. var virginia) Fractions with DPPH and FTC Methods}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {544-548}, type = {Original Article}, chapter = {544}, abstract = {

Introduction: Virginia tobacco (Nicotiana tabacum var. Virginia) is one of the most extensive varieties of tobacco plants. Nicotiana tabacum var. Virginia leaves known to contain alkaloids, saponins, tannins, phenol, flavonoids, triterpenoids and glycosides. In addition to cigarette raw materials, tobacco is also able to be efficacious as an antibacterial, antifungal and bioinsecticide. Objective: The aim of this study to determine the total phenol and total flavonoids and also antioxidant activity of Virginia tobacco leaves fractions. The fraction with the largest compound content was evaluated further for its antioxidant activity. Methods: Virginia tobacco leaves was fractioned into dichloromethane (DCM), ethyl acetate, butanol and water fractions. Phenol levels were determined with Follin-Ciocalteu reagent using the UV-Vis spectrophotometer method measured at 743.50 nm and gallic acid as a reference compound. Total flavonoid levels were determined with AlCl3 reagent using the UV-Vis spectrophotometer method measured at 434.50 nm and quercetin as a reference compound. Antioxidant activity was evaluated with DPPH and Ferric Thiocyanate (FTC) method and the standard used was quercetin. Results: Total phenol levels in Virginia tobacco leaves of DCM, ethyl acetate, butanol and water fractions respectively were 191.2386 mgGAE/g, 201.2913 mgGAE/g, 180.5714 mgGAE/g, 212.8692 mgGAE/g. Total Flavonoid levels respectively were 6.0927 mgQE/g, 6.9659 mgQE/g, 5.1112 mgQE/g, 8.3346 mgQE/g. Antioxidant of water fraction was evaluated further using DPPH and FTC method with IC50 respectively were 75.9148μg/ml and 67.8972 μg/ml. Conclusion: Overview of total phenol and flavonoid levels fractions and antioxidant can be used as an additional initial reference for Virginia tobacco leaves development as source of medicinal substances.

}, keywords = {Atherosclerosis, Hylocereus polyrhizus, LDL cholesterol levels, Red dragon fruit peel}, doi = {10.5530/pj.2022.14.69}, author = {Kori Yati and Misri Gozan and Mardiastuti and Vivi Anggia and Rini Prastiwi and Mahdi Jufri} } @article {1911, title = {The Potential of Antivirus Compounds in Gletang (Tridax procumbens Linn.) in Inhibiting 3CLpro Receptor of SARS-CoV-2 Virus by In Silico}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {796-805}, type = {Research Article }, chapter = {796}, abstract = {

SARS-CoV-2 virus has caused pandemic disease since the end of 2019. Virus transmission occurs through droplet and infects the host{\textquoteright}s respiratory tract rapidly. Viral propagation occurs through translation process of genome +ssRNA, then it being replicated forming some new body parts of virus and assemblied into virions that ready to infect. During the replication process, the translated viral genome in the form of polyprotein will be cut into smaller components by proteases, which one is 3CLpro. The presence of the 3CLpro receptor is used in drug development through in-silico molecular docking process to minimize failures before laboratory test. The antivirus compounds that used to inhibit the 3CLpro receptor are from gletang plant (Tridax procumbens Linn.). This study aim is to determine the value of binding affinity, the interaction between compounds and receptor, and the effect of drug components. The research was conducted by in-silico through the molecular docking process of 3CLpro receptor and antivirus compounds of gletang (Tridax procumbens Linn.), including betulinic acid, kaempferol and lignan. The results showed that the binding affinity of betulinic acid was -6.6 kcal/mol, kaempferol was -5.6 kcal/ mol and lignan was -5.4 kcal/mol. The interaction form of compounds and receptor was hydrogen bond, electrostatic, hydrophobic, and van der Waals. Compared to baicalein compound as a positive control with the value of binding affinity was -6.7 kcal/mol and its interaction with 3CLpro receptor, showed betulinic acid, kaempferol and lignan have smaller ability but they have the potential to inhibit the 3CLpro receptor.

}, keywords = {3CLpro receptor, Antivirus, Gletang, In-silico, SARS-CoV-2.}, doi = {10.5530/pj.2022.14.170}, author = {Yuna Islamiati and Yani Suryani and Ayuni Adawiyah and Opik Taufiqurrohman and Viol Dhea Kharisma and Devi Purnamasari and Nunuk Hariani Soekamto and Anny Setijo Rahaju and Kuswati and Riso Sari Mandeli and Kawther Ameen Muhammed Saeed Aledresi and Nur Farhana Mohd Yusof and Maksim Rebezov and Shimanovskaya Yanina and Belyakova Natalia and Dmitriy Kulikov and Gulnara Mullagulova and Rahadian Zainul and Muhammad Thoriq Albari} } @article {1886, title = {Survey on Aromatherapy Among Healthcare Professionals in Morocco}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {666-670}, type = {Research Article}, chapter = {666}, abstract = {

Background: Herbal remedies and more particularly essential oils are increasingly used throughout the world. In Morocco, the practice of aromatherapy is becoming more and more important, but the knowledge, attitudes, and expectations of healthcare professionals towards essential oils have never been studied. Aim: To assess the attitudes, knowledge, and expectations towards essential oils and aromatherapy of Moroccan healthcare professionals. Methods: We conducted a survey among 205 Moroccan healthcare professionals from different categories using an anonymous electronic questionnaire. Results: The participants to our survey have a good general knowledge and 47.8\% of the them have already prescribed or advised essential oils. However, only 10.2\% of them considered essential oils as widely available. Moreover, only 3.9\% of the respondents judged their theoretical knowledge of essential oils and aromatherapy as perfect, 36.6\% considered the lack of information in this field as the limiting factor in prescribing and advising essential oils, and 88.3\% were in favor of integrating aromatherapy into their basic training course. The prescription or advice of essential oils are statistically correlated with age, profession, factors mentioned as limiting the prescription and advice of essential oils, and the theoretical knowledge. Conclusion: Empowering healthcare professionals{\textquoteright} capacities could help them overcome their fears and enable them to offer aromatherapy advice to their patients with confidence. This could also help to expand the use of essential oils in Moroccan healthcare facilities.

}, keywords = {Aromatherapy, Essential oils, Healthcare professionals, Morocco, Survey}, doi = {10.5530/pj.2022.14.151}, author = {Asmae Alaoui Belghiti and Mohamed Yafout and Soukaina Bennis and Amal Ait Haj Said} } @article {1334, title = {Antidepressant-Like Behavioral and Spatial Memory Effects in Peruvian Red Maca (Lepidium meyenii)-Treated Rats}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {81-88}, type = {Original Article}, chapter = {81}, abstract = {

Introduction: Lepidium meyenii, known with the vernacular name of {\textquotedblleft}Maca{\textquotedblright}, is a Brassicaceae family that has been widely used by Peruvian traditional medicine in cases of sexual dysfunction, memory loss, and several other diseases and pathologies. Objetive: The aim of the study was to test the potential effects of aqueous extract of Red Maca (AQ-RM) on antidepressant-like behavioral in male rats and spatial memory in ovariectomized (OVX) rats. Methods: Forced swimming test was used to examine the potential antidepressant AQ-RM activity in male rats. Fluoxetine and amitryptiline were included as reference drugs. Morris Water Maze test was employed to examine the effect of AQ-RM on spatial memory in ovariectomized (OVX) rats. Such effects were compared to exogenous estradiol administration. The potential role of oxidative stress on spatial memory loss was assessed by measuring malondialdehyde (MDA) levels in rats brain homogenates. Results: AQ-RM enhances swimming and climbing activities while reducing the time of immobility in male rats. Meanwhile, it prevents the decrease in the time spent in the target quadrant and displays higher values in the number of crossings in OVX-rats as compared to OVX-control rats. MDA levels in brain homogenates were decreased in OVX-rats receiving AQ-RM. Conclusion: Oral administration of AQ-RM has anti-depressive application in male rats; and increases the ability of learning and memory in OVX rats.

}, keywords = {Antidepressant activity, Forced swimming test, Lepidium meyenii, Morris water maze test, Red Maca, Spatial memory}, doi = {10.5530/pj.2021.13.12}, author = {Roberto O Yba{\~n}ez-Julca and Ivan M Quispe-D{\'\i}az and Daniel Asunci{\'o}n-Alvarez and Kelly S{\'a}nchez-Mu{\~n}oz and Albert Vargas-Go{\~n}as and Jazminy Morote-Guzman and Ronald Yaro-Marcelo and Edmundo A Venegas-Casanova and Rafael Jara-Aguilar and Pedro Buc Calderon and Julio Benites} } @article {1716, title = {Antidiabetic Activity of Extract and Fractions of Castanopsis costata Leaves on Alloxan-induced Diabetic Mice}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1589-1593}, type = {Original Article}, chapter = {1589}, abstract = {

Background: In North Sumatra, Castanopsis costata is commonly used by traditional practitioners for the treatment of diabetes mellitus, however, no studies have been carried out to substantiate this practice. Therefore, this study aims to evaluate the anti-diabetic activity of extract and fractions of C. costata leaves in mice with alloxan-induced diabetes. Methods: Swiss albino mice with alloxan-induced diabetes, were acquired and subjected to the experimental evaluations. Subsequently, the fasting blood glucose levels of the diabetic mice groups treated with glibenclamid, extract and fractions, as well as the untreated group, were evaluated after two weeks of therapy. Results: Based on the results, the ethanolic extract of C. costata considerably reduced the mice{\textquoteright}s blood glucose levels in a dose-dependent manner, at dosages of 25, 50, 100, and 200 mg/kgBW (\% DBGL: 21.10\%, 46.36\%, 58.94\%, and 60.93\%, respectively). In addition, the water fraction of C. costata leaves produced a greater reduction in blood glucose levels (\% DBGL: 78.93\%), compared to the ethyl acetate and n-hexane fractions (\% DBGL: 67.06\% and 58.83\%), respectively. Meanwhile, treatment with the antidiabetic drug, glibenclamide (5 mg/kgBW) produced a 50.75\% reduction in blood glucose levels. Conclusion: Based on the findings, the extract and fractions of C. costata leaves were concluded to exhibit significant anti-diabetic activity. This supported the claim that traditional practitioners in North Sumatra use the plant extract for diabetes treatment.

}, keywords = {Antidiabetic activity, Castanopsis costata, Diabetes mellitus, North Sumatra.}, doi = {10.5530/pj.2021.13.204}, author = {Maulana Yusuf Alkandahri and Dani Sujana and Dadang Muhammad Hasyim and Mareetha Zahra Shafirany and Lela Sulastri and Maya Arfania and Dedy Frianto and Farhamzah and Anggun Hari Kusumawati and Nia Yuniarsih} } @article {1613, title = {Ethno-Medicinal Plants Used for Medication of Jaundice by The Chinese, Dayak, and Malays Ethnic in West Kalimantan, Indonesia}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {July 2021}, pages = {916-923}, type = {Research Article}, chapter = {916}, abstract = {

Knowledge in the utilization of plants as medicine is local wisdom passed down from generation to generation. This study aims to make an inventory of plants that is efficacious in overcoming jaundice which is used by ethnic Chinese, Dayak, and Malay people in West Kalimantan. This research applies ethnobotany and medical ethnobiology approaches by using observation techniques, semi-structural interviews, also recording and documenting plant species to overcome jaundice. There were 23 types of medicinal plants used by ethnic Chinese, Dayak, and Malay people to overcome jaundice. The 23 types of plants obtained were tebu hitam (Saccharum officinarum L.), pisang mas (Musa paradisiaca L.), kacang hijau (Vigna radiata L.), bawang dayak (Eleutherine palmifolia (L.) Merr.), temulawak (Curcuma xanthorrhiza Roxb.), lipan-lipan (Chrysopogon aciculatus (Retz.) Trin), ciplukan (Physalis angulata L.), cha chen chou/ sawi (Plantago mayor L.), inai (Lawsonia inermis L), kunyit (Curcuma domestica Val.), kelapa gading (Cocos eburen Durch), belimbing manis (Averrhoa Carambola L.), ilalang (Imperata cylindrica (L) Beauv.), sia li chi o kin/putri malu kuning (Neptunia oleracea Lour.), ketepeng (Senna alata (L.) Roxb.), putri malu bunga ungu (Mimosa pudica L.), stet ma thio kin/bunga kancing (Urena lobata L.), tebu karak (Saccharum officinarum L.), kumis kucing (Orthosiphon aristatus (Blume) Miq.), empedu tanah/sambiloto (Andrographis paniculata (Burm.f.) Wall. Ex Nees), pegage/pegagan (Centella asiatica L. Urban), kai kut chou/tulang ayam (Clinacanthus nutans (Burm.f.) Lindau), and bambu kuning (Bambusa vulgaris Schrad.).

}, keywords = {Jaundice, Local Wisdom, Medicinal plants}, doi = {10.5530/pj.2021.13.118}, author = {Ruqiah Ganda Putri Panjaitan and Titin and Yohanes Gatot Sutapa Yuliana} } @article {1402, title = {Metformin Potentiates the Antidiabetic Properties of Annona muricata and Tapinanthus globiferus Leaf Extracts in Diabetic Rats}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {May 2021}, pages = {614-619}, type = {Original Article}, chapter = {614}, abstract = {

Background: There is paucity of experimental evidence on the complementary use of standard anti-diabetic drugs with herbal formulations. Materials and Methods: In this study, extracts of Annona muricata (AME) and Tapinanthus globiferus (TGE) were administered with metformin to diabetic rats in order to study the potential complementary effects. Diabetes was induced by a single intraperitoneal (i.p) injection of alloxan (150 mg/kg BW). AME and TGE (200 mg/ kg BW each) and Metformin (100 mg/kg BW) was administered to diabetic rats orally for 21 days. At the end of the study, rats were sacrificed; blood was collected for assessment of lipid profile and kidney function. Results: Treatment of diabetic rats with AME and TGE caused a significant decrease (p \< 0.05) in the concentrations of total cholesterol (TC), triglyceride (TG) and Coronary Risk Index (CRI) with a concomitant increase in High Density Lipoprotein (HDL). Similarly, urea and creatinine concentration decreased in diabetic rats administered plant extracts. Co-administration of the plant extracts with metformin significantly improved lipid profiles and kidney function relative to rats administered metformin alone. Co-administration of AME and TGE extracts with metformin produced significant improvement in biochemical indices of diabetic rats. Conclusion: The results suggest potential synergistic interaction between the plant extracts and metformin. Furthermore, this work provides scientific support for the concomitant use of the plants used in the study with orthodox drugs for the management of diabetes.

}, keywords = {Annona muricata, Diabetes, Drug interaction, Tapinanthus globiferus}, doi = {10.5530/pj.2021.13.77}, author = {Francis O. Atanu and Oghenetega J. Avwioroko and Omotayo B. Ilesanmi and Ojochenemi E. Yakubu} } @article {1726, title = {Online Survey: Prevalence and Attitude of Jordanians Towards Using Herbal Remedies in the Pandemic COVID-19}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1632-1638}, type = {Original Article}, chapter = {1632}, abstract = {

Coronavirus disease 2019 (COVID-19) is a new virus caused by SARS-CoV-2, a coronavirus from the coronavirus family, that can provoke severe respiratory syndrome. The disease became a pandemic in December 2019. Impaired immune modulation is one of the processes implicated in its pathogenesis, which contributes to poor COVID-19 outcomes. Many investigations have been conducted using medication to control coronaviral infections as antiviral agents or immunomodulators. The results of these tests, however, demonstrated that these medications were useless in fighting the disease. Some people believe that using herbal immunomodulators can aid in the prevention or even curing of COVID-19. Based on prior research, in the management of COVID-19, several botanicals may be useful. We go over the patient attitude and benefits of using such herbal remedies in the regimen of treating COVID-19 in Jordan.

}, keywords = {Botanicals., Coronavirus, COVID-19, Herbal immunomodulators, Herbal remedies, Pandemic, SARS-CoV-2}, doi = {10.5530/pj.2021.13.210}, author = {Noha Abd Alkareem Younis Younis and Rania Mohammad Hamam and Amal Mayyas} } @article {1699, title = {Optimization of Solvent Extraction of the Leaves of Premna serratifolia and Quantitation of Premnaodoroside A by Validated TLC-densitometric Method}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1656-1663}, type = {Research Article}, chapter = {1656}, abstract = {

Introduction: The leaves of Premna serratifolia have been widely used in traditional medicine. Its major constituents were iridoid glycosides and phenolic compounds. Antioxidation was one of its reported bioactivities. The aim of this study was to optimize the ethanol concentration used to obtain high quality extracts. Methods: Three sources of leaf samples were separately extracted by 0, 20, 40, 60, 80 and 100\% ethanol. Their content of premnaodoroside A, the major glycoside, was determined by a TLCdensitometric method developed in this study. The content of total phenolic compounds and antioxidants were also determined by Folin-Ciocalteu and DPPH scavenging methods, respectively. Results: The developed TLC-densitometric method showed a good linearity (R2 \> 0.99) in the range of 0.11-0.872 μg/spot. Its limit of detection and limit of quantitation were 0.13 and 0.04 μg/spot, respectively. The method had satisfactory specificity, precision and accuracy. The analysis results of all extracts showed that the 100\% ethanolic extracts exhibited the highest contents of premnaodoroside A (3.23{\textendash}5.25\%), total phenolic compounds (7.56-8.24\% GAE) and antioxidants (4.92{\textendash}6.66\% AAE), but its extractive yields (13.57-19.57\%) were the lowest. Yields of the 40\% and the 80\% ethanolic extracts were the highest in two samples (36.37-45.96\%) and one sample (47.53\%), respectively. Considering of the extractive ability, the 80\% ethanol could extract the highest amounts of all investigated compounds from plant material. Conclusion: The 100\% ethanolic extract possessed the highest contents of the interesting compounds, but the 80\% ethanolic extract had a higher extractive yield. Their benefits and drawbacks must be considered, depending on further application.

}, keywords = {Antioxidation, Extraction optimization, Premna serratifolia, premnaodoroside A, TLCdensitometry, Total phenolic.}, doi = {10.5530/pj.2021.13.213}, author = {Khin Su Yee and Tasamaporn Sukwattanasinit and Uthai Sotanaphun and Penpun Wetwitayaklung and Bunyapa Wangwattana and Worrakanya Narakornwit} } @article {1719, title = {Pharmacognostic Studies of the Leaves and Fructus of Arctium lappa L. (Asteraceae Bercht. \& J. Presl)}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1734-1745}, type = {Research Article}, chapter = {1734}, abstract = {

Introduction: The state quality assurance system ensures the confidence of consumers that the product meets its quality requirements. In this study, pharmacognostic standards of the leaves and fructus of burdock are specified for the first time. Methods: Microscopic analysis was carried out by using the microscope Carl Zeiss. The UV spectrum were measured on an SF-2000 spectrophotometer. Results: Macroscopically, the leaves are heart-shaped, broad-heart-ovate-shaped with a spaced emarginatedserrate or whole edge, with a wide, wedge-shaped, rounded, uneven base, acute apex, green on the outer surface, grayish slightly pubescent on the inner surface. The fructus are obovate or wedge-compressed, slightly curved, the color is brown/black with spots, or variegated with black spots on a gray background. The microscopic examination of the leaves revealed the presence of epidermis, large submerged and non-submerged stomata of the anomocytic type, 2 types of simple unbranched multi-cellular and glandular capitate trichomes; essential oil glands. Microscopic examination of the leaf petiole revealed the presence of 2 types of simple multi-cellular trichomes, epidermis, angular collenchyma, bicollateral bundles, parenchyma. The stomatal index value is 8.28{\textpm}0.81 per 1cm2. The microscopy of the fructus revealed the presence of elongated cells of the pericarp epidermis; mesocarp; endocarp; endosperm with aleurone grains and drops of fatty oil. The qualitative phytochemical analysis of revealed the presence of polysaccharides, tannins, flavonoids, terpenoids, saponins, phenolic acids. Conclusion: Physical and chemical parameters (moisture, extractive value, ash content) were also specified. These specific data are important for establishing diagnostic indicators for standardization, identification, preparation of new quality standards.

}, keywords = {Analitical standarts, Arctium lappa L., Fructus, Leaves, Pharmacognostic standarts, Phytochemical analysis.}, doi = {10.5530/pj.2021.13.224}, author = {Kolomiets Natalia Eduardovna and Korolev Stepan Alexandrovich and Isaykina Nadezhda Valentinovna and Abramets Natalia Yurievna and Kudryavtseva Darya Vladimirovna and Boev Roman Sergeevich and Zhalnina Ludmila Vladimirovna and Ali Abdujalil Kaid Hasan and Bondarchuk Ruslan Anatolevich} } @article {1653, title = {Phytochemical Screening and Anti-Inflammatory Potential of the Organic Extracts from Cleoserrata serrata (Jacq.) Iltis.}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1225-1241}, type = {Research Article}, chapter = {1225}, abstract = {

Cleoserrata serrata is used in Mexican-south traditional medicine to treat chicleros ulcer. The phytochemical profile and the anti-inflammatory effect from four extracts obtained by maceration proccess and of the primary fractions from two extracts are described. In addition, the antioxidant, leishmanicidal and antimycobaterial activities and LD50 from active extracts are reported. Anti-inflammatory activity was evaluated in TPA and carrageenan assays. Ethyl palmitate and γ-sitosterol were detected in Hexanic and CH2Cl2 extracts. Same compounds and stigmasta-3,5-dien-7-one, palmitic acid, phytol acetate and phytol were detected in primary fractions from CH2Cl2:EtOH extract. In this and in MeOH extracts a polyphenolmixture was obtained. The MeOH extract was subjected to acid hydrolysis, and kaempferol, quercetin and scopoletin were detected in organic-phase. Polyphenol-mixture and organic-phase (IC50=3730 and 2338 μg/mL) showed moderate antioxidant activity; meanwhile MeOH extract exhibited scarce activity. In carrageenan model, Hexanic extract and polyphenol-mixture showed ED50=131.46 and 64.89 mg/ kg, respectively. Three extracts were active but not-dose-dependent. In TPA-model, CH2Cl2 extract and polyphenol-mixture showed ED50 \<0.79 mg/ear, and three extracts were active, however the effect was not-dose-dependent. CH2Cl2:EtOH showed antimycobacterial and leishmanicidal activities. The LD50 was \>2 g/kg for all extracts.

}, keywords = {Anti-inflammatory Effect, Antimycobacterial activity, antioxidant activity, Cleoserrata serrata, DL50, Leishmanicidal activity, Organic extract}, doi = {10.5530/pj.2021.13.156}, author = {Mar{\'\i}a del Carmen Ju{\'a}rez-V{\'a}zquez and Alejandro Zamilpa A and Rosalba Le{\'o}n-D{\'\i}az and Mariano Mart{\'\i}nez-V{\'a}zquez and Adolfo L{\'o}pez-Torres and Julieta Luna-Herrera and Lilian Y{\'e}pez-Mulia and Francisco Alarc{\'o}n-Aguilar and Mar{\'\i}a Adelina Jim{\'e}nez-Arellanes} } @article {1619, title = {Phytochemicals and Antioxidant Activities Evaluation of Origanum vulgare (L.) Stem Bark Extracts}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {July 2021}, pages = {965-970}, type = {Research Article}, chapter = {965}, abstract = {

The present study aimed to evaluate phytochemical and antioxidant activity (in vitro and in vivo) of Origanum vulgare (L.) ethanolic extract. The phytochemical test was assessed using the Clule method in ethanol, ethyl acetate, and hexane. In vitro evaluation of antioxidant activity was determined by radical scavenging assay using DPPH (2,2-diphenyl-1-picrylhydrazyl) as an artificial free radical activity. In vivo test was conducted to evaluate the effect of malondialdehyde (MDA) level in blood plasma during maximum physical activity treatment. In vivo test was done using 25 male Sprague Dawley rats in pre and post-test control group design. The phytochemical test of O. vulgare ethanol extract was showed some compounds, such as a flavonoid, alkaloid, triterpenoid/steroid, essential oil, and tannin, then in ethyl acetate and hexane. In vitro assay showed that O. vulgare extract has strong antioxidant activity with an IC50 value of 133.47 μg/mL. While in the in vivo test, the most effective dosage is 20 mg/200 gr B.W., represented by a significant decrease of MDA level (0.509 nmol/mL) before and after treatment. So, the ethanolic extract of clove has potency as an herbal antioxidant because of the low level of IC50 and can decrease the MDA level.

}, keywords = {2, 2-diphenyl-1-picrylhydrazyl, antioxidant activity, Malondialdehyde, Origanum vulgare (L.), Phytochemical}, doi = {10.5530/pj.2021.13.124}, author = {Rosmalena and Putu Ayu Widyastuti and Fatmawaty Yazid and Neneng Siti Silfi Ambarwati and Islamudin Ahmad} } @article {1683, title = {Preparation of Euyrycoma Longifolia Jack (E.L) Tongkat Ali (Ta) Root Extract Hydrogel for Wound Application}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {November 2021}, pages = {1456-1463}, type = {Research Article}, chapter = {1456}, abstract = {

Background: It is undeniable that a lot of patients worldwide suffer from different types of wounds. The complex process of wound healing has a severe effect on the life quality of patients as well as causing an economic load on healthcare institutions. Although the availability of various therapies for managing patients with acute and chronic wounds for the past decade, these therapies are usually expensive and accompanied by undesirable side effects. Hence, the discovery of a new arsenal for wound healing remains a hot topic of research. Recently, plants and their by-products have garnered remarkable attention as a source of therapeutic agents to treat wounds. This is because medicinal plants provide a rich reservoir of phytochemicals that could potentially become affordable and effective therapeutic agents. Eurycoma longifolia Jack or Tongkat Ali (TA), is one of the well-known traditional plants of Malaysia, it has been scientifically proven to have medicinal properties. Hydrogels are hydrophilic polymer networks that can imbibe a significant number of fluids. In comparison to other systems developed for herbal medicines delivery, a unique power possessed by hydrogels is the high-water absorption ability. This ability has favoured the loading of herbal formulations, which are in general hydrophilic in nature, into hydrogels. Objective: The aim of this study is to prepare Eurycoma longifolia Jack (E.l.J) Tongkat Ali (TA) roots hydrogel for wound application. Methods: Authentication of Eurycoma longifolia Jack roots was done by microscopic examination using methylene blue and Lugol{\textquoteright}s iodine solution. Root extraction by Soxhlet technique. In vitro cytotoxicity of ethanol extract of the roots was evaluated in human primary gingival fibroblasts cells. The ethanolic extract was loaded into hydrogel as a suitable dosage form for further wound healing studies. Results: The crude herbal drug sample, TA present the same microscopical characters to that of E. longifolia Jack tap root. Ic50 was 118.5 μg/mL. The hydrogel was prepared using 2\% xanthan gum and ethanol extract of TA was loaded successfully for its later application as a wound healing agent.

}, keywords = {Eurycoma longifolia Jack, Hydrogel, Microscopic examination}, doi = {10.5530/pj.2021.13.185}, author = {Maryam Riyadh Yaseen and Ghasak G Faisal and Azliana Abd Fuaat and Khairunisa Ahmad Affandi and Batoul Alallam and Mohd Hamzah Mohd Nasir} } @article {1721, title = {Styrylpyrone Derivative from Goniothalamus sp.: A Powerful Drug for Fighting Against Herpes Simplex Virus Type 1}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1598-1606}, type = {Original Article}, chapter = {1598}, abstract = {

Background: The emergence of drug resistance towards Herpes Simplex Virus Type 1 (HSV-1) has encouraged scientists to develop novel lower toxicity and highly effective anti-HSV drugs. Styrylpyrone derivative (SPD) is a bioactive compound isolated from the roots and leaves of Goniothalamus sp. It is believed that this compound possesses antiviral properties against HSV-1. Objective: This paper introduces the interaction of SPD towards HSV-1 through in silico study of molecular docking and molecular dynamic simulation. Materials and Methods: Molecular docking is a computational tool which is used to study the molecular interaction between two or more structures. ADME/T properties of the SPD were generated using the SwissADME online tool in which SPD was found to have a good pharmacokinetic profile. Results: Molecular docking study revealed that SPD has a high docking score of -7.9 Kcal/mol. SPD has a strong affinity with the thymidine kinase (PDB id: 1OF1) producing hydrogen bond and non-polar interaction at the target point of amino acid residue. Conclusion: Molecular docking analysis provides new insight into the structure-based design of SPD compounds with better antiviral activity against HSV-1.

}, keywords = {Antiviral, Herpes Virus type 1 (HSV-1), in silico approaches, Molecular docking and Styrylpyrone derivative.}, doi = {10.5530/pj.2021.13.206}, author = {Syaza Safia Fouzi and Noor Zarina Abd Wahab and Leong Chee Yan and Nazlina Ibrahim} } @article {1673, title = {Subchronic Toxicity of Lunasin Targeted Extract (ET-Lun) from Soybean Seed (Glycine max (L.) Merr.): Perspective from Liver Histopathology, SGOT, and SGPT Levels in Sprague Dawley Rats}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {November 2021}, pages = {1384-1388}, type = {Original Article}, chapter = {1384}, abstract = {

Background: Lunasin Targeted Extract (ET-Lun) has a pharmacology effect in inhibiting inflammation by decreasing COX-2 and iNOS expression. ET-Lun could increase apoptosis and decrease dysplasia (p \> 0,05). In addition, ET-Lun could decrease EGFR expression in breast cancer rats. The acute toxicity showed ET-Lun has LD50 more than 5000 mg/kg BW and was practically non-toxic. Objective: this study aimed to determine the subchronic toxicity of ET-Lun. Methods: Male and female Sprague Dawley rats (n=40) were divided into 4 groups, the control group and treatment group ET-Lun dose of 250 mg/Kg BW, 500 mg/kg BW, and 750 mg/kg BW. The ET-Lun was administered for 90 days. On the 91st day, the animals were dissected and examined for SGOT-SGPT levels, liver histopathology, and diameter of the central vein. Results: The SGOT-SGPT levels showed no significant difference between the treatment group and the control group (p \> 0.05). On microscopic observation, there was no change or damage to the liver of rats in each group. The diameter of the central vein of the rat liver shows no significant difference between the control and treatment groups. Conclusion: The ET-Lun does not produce adverse effects in liver rats after subchronic treatment.

}, keywords = {Liver, Lunasin, SGOT, SGPT, Soybean, Subchronic Toxicity}, doi = {10.5530/pj.2021.13.175}, author = {Numlil Khaira Rusdi and Weri Lia Yuliana and Erni Hernawati Purwaningsih and Andon Hestiantoro and Kusmardi Kusmardi} } @article {1393, title = {Synthesis of Novel pyrimido[4,5-b]quinoline-4-one Derivatives and Assessment as Antimicrobial and Antioxidant Agents}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {March 2021}, pages = {550-562}, type = {Research Article}, chapter = {550}, abstract = {

Objective: Antimicrobial resistance has emerged as one of the serious global health problems of the 21st century that threatens the efficient treatment and prevention of an everincreasing range of infections caused by bacteria, viruses, and fungi. Therefore, it would be favorable to find promising agents with antioxidant and antimicrobial activity combined in one molecule. Key findings: Pyrimido[4,5-b] quinolines are biologically active compounds that are known to rely primarily on the functional group{\textquoteright}s existence and location. Quinolinbenzo-[ 1,3]oxazin-4-one (3) was prepared and played as electrophilic interface/mediator for the synthesis of many compounds, such as pyrimido[4,5-b]quinoline, quinoline-carboxamide and oxoquinazolin-acetamide by reacting with nucleophilic reagent. Summary: Results revealed that pyrimido[4,5-b] quinoline derivatives (17b, 9d and 9c) are the most potent compounds that displayed significant antimicrobial activity along with compounds 17a, 29b, 5, 19, 23b, and 25b that appeared to be more promising as antioxidant agents than ascorbic acid.

}, keywords = {antimicrobial agent, Antioxidant agent, Benzoxazinones, Pyrimidoquinolin, Quinoline}, doi = {10.5530/pj.2021.13.69}, author = {Usama Fathy and Rasha S Gouhar and Ahmed Younis and Dina H El-Ghonemy} } @article {1077, title = {Activity of Kincung Flowers (Etlingera Elatior (Jack) R.M.Sm.) on Total Leukocytes and Percentage of Leukocytes in Allergic Male White Mice}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {44-51}, type = {Original Article}, chapter = {44}, abstract = {

Introduction: Kincung Flower (Etlingera elatior (Jack) R.M.Sm.) is a native herbal plant in Southeast Asia that traditionally used to many diseases, especially in Indonesia. Aim: This study was conducted to determine the activity of kincung (Etlingera elatior (Jack) R.M.Sm.) on the total number of leukocytes and differential leukocyte cells in allergic mice. Material and Methods: The semi-solid extract of Kincung flower (Etlingera elatior (Jack) R.M.Sm.) was made by the maceration method using 70\% ethanol solvent. The animals used were 20 male white mice that have allergies of skin that treated with 20\% albumen antigens given on the first day 0.2 mL/20 g intraperitoneally, then on the seventh day are given antigens with the same dose subcutaneously. Allergic mice indicated by redness at the injection site. It divided into four groups: the negative control group and three dose groups (100; 300; and 1000 mg/kg). On the seventh day after administration of the extract, observed the value of total leukocytes and differential leukocyte cells in mice. Results: The results after administration of extracts in 3 dose groups (100; 300; and 1000 mg / kg) and the negative control group showed sequentially the total number of leukocytes was: 3.95; 4.73; 6.01; and 3.6 x103/μL and the percentage of leukocytes consisting of lymphocytes: 67.6\%; 62.0\%; 56.8\% and 70.0\%, neutrophils: 22.4\%; 29.2\%; 36.8\% and 20.0\%, eosinophils: 6.4\%; 5.8\%, 4.2\% and 6.6\%, monocytes: 3.6\%; 3.0\%, 2.2\% and 3.4\%, and basophils: 1.8\%; 1.4; 0.8\% and 2.0\%. It concluded that kincung flowers could increase total leukocytes significantly (p\<0.05), decrease lymphocytes, eosinophils, basophils significantly (p\<0.05), increase neutrophils significantly (p\<0.05), and reduce monocytes insignificantly (p\>0.05). Conclusion: Kincung flowers (Etlingera Elatior (Jack) R.M.Sm.) can be used as an immunomodulator and decreasing the percentage of basophil cells, and eosinophils can used as an anti-allergic drug.

}, keywords = {Allergies, Etlingera elatior (Jack) R.M.Sm, Kincung Flower, Leukocyte Percentage, Mice, Total Leukocytes}, doi = {10.5530/pj.2020.12.8}, author = {Yufri Aldi and Elidahanum Husni and Relin Yesika} } @article {1146, title = {Ameliorative Effect of the Oral Administration of Chuquiraga spinosa in a Murine Model of Breast Cancer Induced with 7,12-Dimethylbenz[a]anthracene (DMBA)}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {May 2020}, pages = {562-568 }, type = {Research Article}, chapter = {562}, abstract = {

Objective: To determine the ameliorative effect of the ethanolic extract of Chuquiraga spinosa (ChS) on 7,12-Dimethylbenz[a]anthracene (DMBA)-induced breast cancer in rats. Methods: 36 female Holztman rats were divided into 6 groups. I) The negative control group received physiological saline (PS). II) ChS-200 group received 200 mg/kg of ChS. III) DMBA group was induced with DMBA (20 mg/Kg) dissolved in PS and administrated orally for 15 weeks. IV) DMBA + ChS-50 group, V) DMBA + ChS-250 group, and VI) DMBA + ChS-500 group, which received the extract orally for 15 weeks after DMBA induction. All data were expressed as mean and standard deviation. One-way analysis of variance (ANOVA) followed by Dunnet test was carried out to compare the mean value of different groups Histopathological analysis was evaluated by using Image J software. Results: Hematology showed that the triglyceride level was significantly lowered (P\< 0.01) and high-density lipoprotein (HDL) level was significantly increased (P \<0.01) in groups III, IV and V. Also, ChS extract significantly lowered the C reactive protein (CRP) level (P \<0.01) and malondialdehyde level (P\<0.05). There was a significant decrease in the frequency of DMBA-induced micronucleated polychromatic erythrocyte (P\<0.01). Conclusions: Chuquiraga spinosa showed an ameliorative effect on DMBA-induced breast cancer in rats as well as antioxidant, antitumor and antigenotoxic properties.

}, keywords = {Anticarcinogenic agent, Antioxidant, Breast tumor, Phytochemical, Preventive medicine, Toxicity}, doi = {10.5530/pj.2020.12.85}, author = {Jorge Luis Arroyo-Acevedo and Oscar Herrera-Calderon and Johnny Aldo Tinco-Jayo and Juan Pedro Rojas-Armas and Abdur Rauf and Ren{\'a}n Ha{\~n}ari-Quispe and Linder Figueroa-Salvador and Victor Fern{\'a}ndez-Guzm{\'a}n and Ricardo {\'A}ngel Yuli-Posadas} } @article {1110, title = {Antidiabetic and Antioxidant Effect Combination Vasconcellea pubescens A.DC. and Momordica charantia L. Extract in Alloxan- Induced Diabetic Rats}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {311-315}, type = {Original Article}, chapter = {311}, abstract = {

Introduction: Mountain papaya (Vasconcellea pubescens A.DC.) and bitter melon (Momordica charantia L.) fruit extract have total flavonoids and some metabolite from its contains. The use of a single dose in the treatment of diabetes is often considered to lack a strong effect. Giving a combination of the compound is a solution to provide a synergistic effect in treatment. Material and Methods: Rat were divided into eight groups (normal, negative control, glibenclamide as a positive control, and five dose extract group). The single dose mountain papaya extract (MPE) and bitter melon extract (BME) were given at 174 mg/kg b.w of MPE, and 380 mg/kg b.w of BME in oral administration. Combination of MPE:BME (25:75, 50:50, 75:25)\% or (87:190; 44:285 and 130:95) mg/kg b.w in oral administration. Induction of diabetes used alloxan dose of 150 mg/kg b.w intraperitoneally. The treatment was performed for 21 days with a frequency of once a day. Blood sugar level was measured at pretest, 7th, 14th, and 21st days. At the end of the test, measurements of malondialdehyde (MDA), glutathione (GSH), and pancreatic morphology were measured. Data were analyzed by ANOVA statistic. Results: The single and combination of MPE-BME showed an decrease in blood glucose levels significantly compared with the negative control (p <= 0.05). The same results from measurements of levels of malondialdehyde (MDA), glutathione (GSH), and pancreatic morphology. Conclusions: Based on the research, a combination of the MPE-BME had antidiabetic and antioxidant activity, but the activity was not significantly different from both single-dose extract (p\> 0.05).

}, keywords = {Antidiabetic, Antioxidant, Flavonoids, Momordica, Synergistic, Vasconcellea}, doi = {10.5530/pj.2020.12.49}, author = {Heru Sasongko and Ratih Guswinda Lestari and Adi Yugatama and Yeni Farida and Sugiyarto} } @article {1295, title = {Chemical Constituents from Diospyros discolor Willd. and their Acetylcholinesterase Inhibitory Activity}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1547-1551}, type = {Original Article}, chapter = {1547}, abstract = {

Background: Diospyros discolor is commonly known as {\textquoteleft}buah mentega{\textquoteright} and traditionally used to treat various diseases. Many compounds especially triterpenes in Diospyros sp. were reported to inhibit acetylcholinesterase (AChE) and butyrylcholinesterase enzymes in vitro and in vivo. D. discolor was reported to contain triterpenes, yet to be investigated for their AChE inhibitory activity. D. discolor leaves extract showed high (95.80 {\textpm} 1.57 \%) AChE inhibitory activity at the concentration of 100 μg/mL. Objective: The aim of the present study is to identify chemical constituents from D. discolor and their AChE inhibitory activity. Materials and Methods: The leaves and stem barks of D. discolor were air dried, powdered and successively extracted using n-hexane, dichloromethane and methanol. The solvents were evaporated to obtain dried crude extracts. The compounds were purified using exhaustive chromatographic procedures and their structures were determined by analyses of spectral data. The AChE inhibitory activity was carried out using Ellman{\textquoteright}s method. Results: A new flavonol, 7,4{\textquoteright}-dihydroxy-5,3{\textquoteright},5{\textquoteright}-trimethoxyflavonol (1), along with five known flavonoids (2-6) and six known triterpenes (7-13) were isolated from the leaves and stem barks of D. discolor. Selected compounds were evaluated for AChE inhibitory activity, in which stigmast-4-ene- 3-one (7) showed the lowest inhibition concentration with an IC50 value of 11.77 {\textpm} 2.11 μM. Conclusion: A new flavonol (1) and twelve known compounds were identified and characterized. Even though D. discolor extracts showed high percent inhibition against AChE enzyme, the isolated compounds showed moderate inhibition.

}, keywords = {Acetylcholinesterase, Ebenaceae, Flavonoid, Triterpenes}, doi = {10.5530/pj.2020.12.212}, author = {Norhafizoh Abdul Somat and Zaini Yusoff and Che Puteh Osman} } @article {1092, title = {Efficacy of Allium sativum, Curcuma mangga and Acorus calamus Extract Combination on Rat Fertility}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {197-203}, type = {Research Article}, chapter = {197}, abstract = {

Objective: to evaluate the efficacy of Allium sativum, Curcuma mangga, and Acorus calamus extract combination on female rat fertility. Methods: Thirty-six female rats were randomized divided into 9 groups (n=4): C- (no treatment); C+ (clomiphene citrate); composition 1 (A. sativum 36\%: C. mangga 36\%: A. calamus 28\%) with 3 doses i.e T1, T2 \& T3 of 50, 75 \& 100 mg/kg BW; composition 2 (A. sativum 35\%: C. mangga 40\%: A. calamus 25\%) with 3 doses i.e T4, T5 \& T6 of 50, 75 \& 100 mg/kg BW and T7 (Subur Kandungan herb{\texttrademark}). Treatment was given every day for 15 days. Results: The results revealed that all treatments affected reproductive hormone and uterine histology profile. However, T1 produced the highest estrogen and progesterone levels, and T2 produced the highest endometrial and myometrium thickness, as well as the number of endometrial glands. Furthermore, the hormonal profile in T1 and histological profile of uterus in T2 were not significantly different from those of T7 group. Conclusions: Combined A. sativum, C. mangga, and A. calamus extracts could be used to increase fertility in female rat. The most effective treatment in this study was dose of 50-75 mg/BW in both compositions.

}, keywords = {Acorus calamus, Allium sativum, Curcuma mangga, Fertility, Rat}, doi = {10.5530/pj.2020.12.30}, author = {Bayyinatul Muchtaromah and Roihatul Muti{\textquoteright}ah and Desy Rahma Yusmalasari and Putri Mardyana and Tanjina Sharmin} } @article {1303, title = {Evaluation of Myrmecodia pendans Water Extracts on Hematology Profiles, Liver, Kidney Function and Malondialdehyde Level in Healthy Volunteer}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1489-1493}, type = {Original Article}, chapter = {1489}, abstract = {

Background: Ant Nest (Myrmecodia pendans) is one of plants that have been used by locals in Indonesia to empirically treat various diseases. Ant Nest in vitro and in vivo studies on animals have been widely reported its pharmacological activities as an antioxidant. Unfortunately, scientific proofs reported on this plant as human medicine are still lacking. Aim: This study aimed to ensure effectiveness, and safety due to administration of Ant Nest Water Extract (ANWE) formulated in capsule. Materials and Methods: Twelve volunteers were divided into 2 groups, 6 volunteers in each group. Group I: Ant Nest Water Extract Capsule (ANWEC) in dose of 350 mg ANWE, and group II: Placebo Capsule (PC) which contained 350 mg amylum. Each groups given the capsule once daily for 28 days. The comparison was made between group I and group II. Hematology tests include hemoglobin, leucocyte and thrombocyte. Blood chemistry tests include SGOT, SGPT, total cholesterol, triglycerides, HDL, LDL, glucose, ureum (Ur) and creatinine (Cr). Malondialdehyde (MDA) level was measured at day-28 which was the last day of the intervention. Results: After 28 days administration of ANWE, the SGOT, SGPT, Ur, and Cr showed in normal level as follows SGOT (U/L): 19.2 {\textpm} 3.99; SGPT (U/L): 17.2 {\textpm} 6.80; Ur (mg/dL): 19.75 {\textpm} 3.66; Cr (mg/dL): 1.06 {\textpm} 0.13. MDA (ng/mL) level in ANWEC-treated group was significantly lower (117.2{\textpm}23.8) than PC (147.25{\textpm}18.7). There was no intolerable complaints during the observation. Conclusion: The study concluded that Water Extract of Ant Nest 350 mg has no damage to liver, kidney and hematology, so it was proven that this plant is safed to be consumed by human for its potency as antioxidant.

}, keywords = {Antioxidant, Malondialdehyde, Myrmecodia pendans, Safety}, doi = {10.5530/pj.2020.12.204}, author = {Tri Widyawati and M Aron Pase and Milahayati Daulay and Imam Bagus Sumantri and Nor Adlin Yusoff} } @article {1164, title = {The Extract of Kincung Flower (Etlingera elatior (Jack) R.M.Sm.) Activity to Decrease IL-4 and IgE Levels in Type I Hypersensitivity White Male Mice}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {682-686}, type = {Original Article}, chapter = {682}, abstract = {

Introduction: Kincung Flower (Etlingera elatior (Jack) R.M.Sm.) is a herbal plant which contains many secondary metabolites. It showed to suppress allergic reactions by inhibiting mast cell degranulation, active cutaneous anaphylaxis and decreasing the number of basophils and eosinophils. Aim: The study conducted to determine the decreased IL-4 and IgE level of type I hypersensitivity male white mice using kincung flowers extract. Materials and Methods: The maceration method used to make ethanol extract of Kincung flower (Etlingera elatior (Jack) R.M.Sm.). The research used 25 allergic male white mice, which made by injected 20\% albumen that given on the first day 0.2 mL/20 g intraperitoneally. On the seventh day are given albumen with the same dose subcutaneously. The characteristic of the allergic mice is the redness at the injection site. It divided into five groups: the negative control group, the positive control group and three dose groups (100; 300; and 1000 mg/kg). After mice given extract for seven days, then measured IgE and IL-4 levels in the serum of mice. Results: The results after three dose groups (100; 300; and 1000 mg/kg) given, the negative and positive control group showed sequentially the IL-4 level was: 33.024; 27.933; 25.192; 23.130 and 41.538 ng/ mL. And IgE level in serum was 0.944; 0.629; 0.210; and 1,597 μg/ mL. Conclusion: It concluded that kincung flowers decreased IL-4 and IgE level significantly (p\<0.05). So it could use as an anti-allergic drug.

}, keywords = {Allergies, Etlingera elatior (Jack) R.M.Sm, IgE, IL-4, Kincung Flower, Mice}, doi = {10.5530/pj.2020.12.100}, author = {Elidahanum Husni and Relin Yesika and Yufri Aldi} } @article {1289, title = {In vitro Propagation and Determination of Total Phenolic Compounds, Flavonoid Contents and Antioxidative Activity of Globba globulifera Gagnep}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1740-1747}, type = {Research Article}, chapter = {1740}, abstract = {

Introduction: Currently, there is a reduction in the number of Globba globulifera, which is due to its slow multiplication rate, high susceptibility to pathogenic diseases and overexploitation of the plant from natural sources. In vitro culture to study suitable concentrations of plant growth regulators for shoot and root induction of G. globulifera. Bioactive compounds were measured by TPC, TFC and FRSA methods for comparison of those from in vitro and natural conditions. Methods: Microshoots were cultured on solid and liquid MS medium supplemented with various concentrations of cytokinins (BA, Kinetin and TDZ) and auxins (NAA and IBA) for eight weeks. Methanol was used as the extraction solvent via the ultrasonic method, TPC and TFC were both measured. DPPH for free radical scavenging activity was investigated. Results: The best result for shoot formation was achieved when culturing on MS medium with 3 mg/l and 5 mg/l of BAP or 5 mg/l of BAP plus 1 mg/l of IBA. The plantlets were transplanted to pots in a greenhouse. All the planting material showed a 100\% survival rate. The rhizomes of in vitro derived plantlets showed the highest value of TPC (52.28 mg GAE/g crude extract) and FRSA (93.55\%) and lowest of IC50 (0.46 mg/ml). Conclusion: The in vitro culture and antioxidant activity analysis could be the foundation for plant propagation in large quantities and the use of medicine.

}, keywords = {Bioactive compound, DPPH, Micropropagation, TFC, TPC, Zingiberaceae}, doi = {10.5530/pj.2020.12.236}, author = {Wipa Yaowachai and Surapon Saensouk and Piyaporn Saensouk} } @article {1168, title = {Microencapsulation of Macaranga gigantea Leaf Extracts: Production and Characterization}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {716-724}, type = {Original Article}, chapter = {716}, abstract = {

Introduction: The aim of this research was to formulate the microcapsules of Macaranga gigantea leaves extract with solvent evaporation method using Ethocel 10 cP and Eudragit E100 as matrix. Methods: M. gigantea leaves were extracted using ethanol 96\%. This extract was dried by rotary evaporator. The microencapsulation process of M. gigantea leaves extract was conducted by solvent evaporation method (O/W: oil in water). The formula of M. gigantea leaves extract microcapsules were designed into six formulas (Eudragit E100: FA1, FA2, FA3 and Ethocel 10 cP: FB1, FB2, FB3). Microcapsules of M. gigantea leaves extract were characterized for particle size, in terms of surface morphology by scanning electron microscope (SEM) and encapsulation efficiency. Antioxidant activity of the formulation have been evaluated by DPPH method. Physical characterization on microparticles were performed by conducting entrapment efficiency and SEM picture. Results: In this research, the micoparticles containing M. gigantea extract has been developed by using ethyl cellulose (Ethocel 10 cP ) and eudragit (Eudragit E100) as polymer matrix. The results showed that high concentration of polymer (Ethocel 10 cP and Eudragit E100) used in microencapsulation resulted in better M. gigantea leaves extract microcapsules in terms of physical characteristics. Particle size of microcapsules containing M. gigantea leaves extract were in the range of 3.564 to 5.887 μm. Encapsulation efficiency (\% EE) was categorized as good because the value were >= 80\% to which 85.978\% (FA3) and 88.992\% (FB3). SEM picture of FA3 (Eudragit E100) revealed that the surface of microcapsule were rough and porous. When Ethocel 10 cP used as polymer, a smoother surface and less visible pores of microcapsule were obtained. The antioxidant ability of M. gigantea leaves extract microcapsule showed that IC50 values was 64.51 ppm. Conclusion: It can be concluded that microcapsules of M. gigantea leaves extract can be prepared by solvent evaporation method by using Eudragit E100 and Ethocel 10 cP as polymer matrix. M. gigantea leaves has potent antioxidant activity either as extract or after formulated into microcapsules.

}, keywords = {Antioxidant, Ethocel 10 cP, Eudragit E100, Macaranga gigantea, Microencapsulation, Solvent evaporation method}, doi = {10.5530/pj.2020.12.104}, author = {Muhaimin Muhaimin and Yusnaidar Yusnaidar and Wilda Syahri and Madyawati Latief and Anis Yohana Chaerunisaa} } @article {1140, title = {Online Survey for Patient Outcomes on Hericium Erinaceous Mushroom}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {May 2020}, pages = {519-525 }, type = {Original Article}, chapter = {519}, abstract = {

Hericium Erinaceous (Lion{\textquoteright}s Mane) mushroom is steadfast becoming one of the most widespread and familiar of medicinal mushrooms currently available worldwide, this could be due to its many surprising health benefits and it is the ability to treat various ailments. In our study, we connected a questionnaire to the largest internet portal for Hericium Erinaceous (H.Erinaceous) consumers to measure respondents{\textquoteright} feedback. The questionnaire addresses the attitude and potential benefits of respondents towards H.Erinaceous intake by using a numeric rating scale (NRS),97respondents took part in our study. The most frequently used of H. Erinaceous in our sample were in the treatment of neural diseases, enhance memory and GI disorders. The benefits and satisfied outcomes were highest with participants who use H. Erinaceous in a dose of 2-3 tablets (3g) twice/day to improve memory and cognitive properties and lowest in the treatment of autism even with high doses. 69.9\%of participants did not discuss consuming this mushroom with their physician. Objectives for the study to determine the prevalence and purposes of using the mushroom in different diseases and to predict the outcomes, side effects and the most effective dose taken by participants.

}, keywords = {Hericium Erinaceous, Lion{\textquoteright}s Mane, Medicinal mushrooms, Numeric rating scale}, doi = {10.5530/pj.2020.12.79 }, author = {Noha Abd Al Kreem Younis Younis} } @article {1299, title = {A Perspective Overview on Hygrophila auriculata}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1748-1752}, type = {Review Article}, chapter = {1748}, abstract = {

Hygrophila auriculata, belonging to the family Acanthaceae, is a promising medicinal plant with great economic potential. The medicinal value of H. auriculata has been appreciated in the ancient medical literature. The plant contains terpenoids, alkaloids, flavonoids, and is traditionally known as an aphrodisiac, renal tonic, and for its health-promoting properties. The plant is cultivated throughout India. However, systematic information on the different aspects of this species is not available. In this review, an attempt has been made to present this information.

}, keywords = {Hygrophila auriculata, Pharmacological activity, Phytochemistry}, doi = {10.5530/pj.2020.12.237}, author = {S Dhanalakshmi and N Harikrishnan and N Srinivasan and P Pandian and BA Tanisha and M Tharun Kumar and V Lokesh and N Yuvashri and S Supriya} } @article {1144, title = {Pharmacognostic Studies on Methanolic Extract of Leaves of Vitex negundo Linn}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {May 2020}, pages = {551-556}, type = {Research Article}, chapter = {551}, abstract = {

Vitex negundo Linn (verbenaceae), known as Nirgundi is important medicinal plant with variety of phytoconstituents having significant pharmacological activities. It has antiinflammatory, analgesic, anti-histaminic, anti-oxidant, anti-bacterial, hepatoprotective, antiimplantation, laxative, larvicidal, anti-arthritic, anticonvulsant and effective against snake venom activity. Two compounds namely vitexin and negundoside are reported to have anticancer and hepatoprotective activity respectively. For safe and effective use of herbal drugs in a formulation, proper standardization of herbal drugs is necessary. So, in this research paper basic pharmacognostic studies on Vitex negundo leaf extract like physicochemical parameters- ash values and extractive values, Fluorescence analysis, phytochemical screening, TLC profile with different solvent systems, behavior with different reagents and metal analysis was done. The findings throw light on preliminary standardization of this important medicinal plant. Key

}, keywords = {Ash values, Extractive values, Fluorescence analysis, TLC, Vitex negundo (VN)}, doi = {10.5530/pj.2020.12.83 }, author = {Kiran Sharma and Manish Yadav and Kavita Attri} } @article {1106, title = {Prospects for the Use of Spinach (Spinacia oleracea L.) Containing Phytoecdysteroids and Polyphenols}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {246-250}, type = {Original Article}, chapter = {246}, abstract = {

Background: Phytoadaptogens, biologically active compounds increasing the nonspecific resistance of the human organism, are well known for the prevention and correction of stressful conditions. Phytoadaptogens group includes phytoecdysteroids and polyphenols, that are characterized by the multiplicity of pharmacological effects in combination with the low toxicity. According to literature data, spinach (Spinacia oleracea L.) is a promising source of these compounds. This work aims to systematize data on the chemical composition of biologically active compounds of spinach, that determine its adaptogenic properties and concentration methods in the spinach processing for use in specialized foods and dietary supplements. Materials and Methods: Manifold electronic search engines, electronic databases, and libraries such as Google, Google scholar, Crossref, Indian Science Abstracts, Emerging Sources Citation Index, e-Library, Scopus, Web of Science, Pubmed, Chemical Abstracts, Index Copernicus, scientific literature had been searched and data obtained. Results: Botanical characteristics of spinach, main cultivation conditions, the latest data on the chemical composition of raw spinach material cultivars and extracts based on it are presented in this study. Schemes for the obtaining of products enriched with polyphenols and ecdysteroids are considered, and ways of proper purification are mentioned. Conclusion: It is recommended to introduce spinach into the diet of healthy people in order to increase the functional reserves of a person during periods of hypovitaminosis, overwork, intense physical exertion, and also to compensate for the adverse effects of external factors. Spinach extracts containing phytoecdysteroids (20-hydroxyecdysone) and polyphenols (flavonoids) can be used as a prophylactic to overcome the negative effects of stress, accelerate recovery after strong physical and mental stress, particularly for people with extreme occupations, athletes, and those who are engaged in hard physical labor.

}, keywords = {20-hydroxyecdysone, Flavonoids, Phytoecdysteroids, Polyphenols, Spinach leaves, Spinacia oleracea}, doi = {10.5530/pj.2020.12.38}, author = {Bokov DO and Sidorova YuS and Mazo VK and Bessonov VV} } @article {1104, title = {Study of Quality Medicinal Plants Bark Walnuts and Extract from it}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {282-286}, type = {Original Article}, chapter = {282}, abstract = {

Objective: The bark of walnut is currently poorly understood and is not represented in the Russian State Pharmacopeia. The purpose was to study the quality indicators medicinal plants walnut crust and extracts therefrom were studied: moisture content, total ash, ash insoluble in 10\% hydrochloric acid feedstock walnut crust; content of tannins and juglone in walnut crust; GC-mass spectrometric study of the composition petroleum extract from the bark of a walnut. Materials and Methods: Microscopy was prepared by the pharmacopoeial method. The chemical composition of the petroleum extract was investigated by chromatomass spectrometry. Results: The content of glycosides amount in terms of gidroyuglone glucoside and absolutely dry RL was 5.30 {\textpm} 0.15. Humidity was 9,41\% {\textpm} 0,21. total ash content was 10,18\% {\textpm} 0,1. The ash content insoluble in 10\% hydrochloric acid was 4.8 {\textpm} 0.16. Gas chromatography-mass spectrometry method in petroleum extraction from the bark of walnut were identified following compounds: oktadetsilgeksanoat (28\%) of 4-isopropenyl- 1-methyl-2-cyclohexenol-1 (38\%), cineole (1,6\%), thujone (0.7\%), camphor (16.6\%), 2 - benzamidoantrahinone (0.45\%), 4,5 - dihydroxy - 3,4 - dihydro - 1 (2H) - naftalenon (6.4\%) ethyl ester of palmitic acid (8.25\%) Toxic effects petroleum extract was TD50 = 2,5. Chronic absent. All mice in the experimental group had diarrhea. It was established that the extraction has petroleum anthelmintic properties at askaridioze. Conclusions: The analysis of petroleum extraction from walnut partitions was carried out, the content of basic biologically active substances was revealed. The main anatomical and diagnostic signs of walnut bark walls were studied.

}, keywords = {Juglans regia, Total ash, Toxic effect}, doi = {10.5530/pj.2020.12.44}, author = {Strelyaeva AV and Lezhava DI and Luferov AN and Kuznetsov RM and Bobkova NV and Lazareva YuB and Kostikova EN} } @article {1069, title = {Subacute Toxicity of Butanol Fraction of Tali Putri Plants (Cassytha filiformis L.) Against Hematology Parameters of White Male Mice}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {25-28}, type = {Original Article}, chapter = {25}, abstract = {

Hematotoxicity study of butanol fraction of Cassytha filiformis L. on white male mice has been performed. A total of 12 white male mice were used, and they were divided into four groups. Each group consists of 3 mice. These animals were treated with Cassytha filiformis L. butanolic fraction at several doses of 2.5, 5, and 10 mg/kg for seven days. Hemoglobin value, erythrocytes, platelets, leukocytes, monocytes, lymphocytes, eosinophils, neutrophils, and basophils counts were measured at the 1st, 3rd, and 7th day of treatment. The data of this study were analyzed using two-way ANOVA, followed by Duncan{\textquoteright}s multiple region tests. The results showed that the doses of butanol fraction did not affect hemoglobin value, erythrocytes, leukocytes, and neutrophils (p \>0.1), but it significantly reduced platelet, monocyte, lymphocyte count, and increases eosinophils (p \<0.01) counts within their normal limits. There is no influence on the duration of administration and the interaction of dosage, and also the duration of use of the parameters above. This result implies that the Cassytha filiformis butanol fraction at doses of 2.5-10 mg/kg does not affect hematology parameters if it were used for seven days.

}, keywords = {Butanol fraction, Cassytha filiformis L, Haematology, Subacute toxicity}, doi = {10.5530/pj.2020.12.5}, author = {Dwisari Dillasamola and Annisa Yatursyi and Armenia} } @article {894, title = {Antioxidant Activity of the Germinated Seed of Four Varieties of Amaranthus Caudatus L. from Peru}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {May 2019}, pages = {588-593}, type = {Original Article}, chapter = {588}, abstract = {

Introduction: The objective of this study was to determine the antioxidant activity of four varieties of germinated seeds of Centenario, Cristalino, Oscar Blanco and Taray of Amaranthus caudatus L. compared to non-germinated seeds. Material and Methods: The determination of total phenols was carried out by using Folin-Ciocalteu, total flavonoids by the method of aluminum chloride and the antioxidant activity by the methods of DPPH, ABTS and FRAP. Results: Cristalino variety had the highest germination (3.0 cm of height) and all varieties had a 50\% germination rate. Cristalino and Taray varieties had the highest content of total phenolics (GAE 32.92 and 35.00 mg/g sample), Cristalino variety had higher content of flavonoids (580.95 mg QE/g) (P \< 0.05); Cristalino and Taray varieties showed greater scavenging activity of DPPH radical (151.85 and 151.38 mg TE/g sample), ABTS (178.09 and 180.18 mg TE/g sample); and reducing capacity of the ferric ion (FRAP) (132.75 and 136.42 mg TE/g of sample). Conclusion: Sprouts of Cristalino and Taray varieties had higher antioxidant activity than non-germinated seeds and they are directly related to higher content of total phenols and flavonoids.

}, keywords = {Amaranthus caudatus L., antioxidant activity, Germinated seeds, Phenolics}, doi = {10.5530/pj.2019.11.93}, author = {Enrique Javier Aguilar-Felices and Marta Romero-Viacava and Edwin Enciso-Roca and Oscar Herrera-Calderon and Pablo Com{\'u}n-Ventura and Ricardo {\'A}ngel Yuli-Posadas and Luz Chacaltana-Ramos and Bertha Pari-Olarte} } @article {787, title = {Antioxidant and Anti-inflammatory Activities of Bauhinia ungulata L. (Fabaceae) on LPS-Stimulated RAW 264.7 Cells}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {January 2019}, pages = {37-42}, type = {Original Article}, chapter = {37}, abstract = {

Objective: The present study aimed to investigate the antioxidant, immunomodulatory and antimicrobial activities of Bauhinia ungulata L. Method: A flavonoid-rich fraction was obtained from the Bauhinia ungulata L stem, called the ethyl acetate fraction of Bauhinia ungulata (FABU). The total antioxidant capacity of the FABU was determined through the phosphomolibdenium reduction method. For the evaluation of its antioxidant activity on a cell culture model, LPS-stimulated RAW 264.7 cells were treated with different concentrations of FABU and the reactive oxygen species (ROS), nitric oxide (NO), hydrogen peroxide (H2O2) and thiobarbituric acid reactive substances (TBARS) production levels were measured. For the analysis of its immunomodulatory capacity, TNF-α, TGF-β and IL-10 levels were determined in the culture supernatant. In order to determinate the antimicrobial activity of FABU, antifungal and antibacterial susceptibility testing was performed against Candida albicans, methicillinsensitive Staphylococcus aureus, methicillin-resistant Staphylococcus aureus and Pseudomonas aeruginosa strains. Result: The FABU demonstrated neither significant antimicrobial activity nor immunodulatory capacity; on the other hand, its potential antioxidant activity was demonstrated by the phosphomolibdenium reduction assay. Also, FABU treatment inhibited the ROS, NO, H2O2 and TBARS levels in the supernatant of LPS-stimulated cells. Conclusion: A significant reduction in the amount of reactive oxygen and nitrogen species (RONS) was observed, in addition to lipid peroxidation inhibition. Our data suggest that the FABU is a natural antioxidant complex that may interfere in the cascade of cell damage caused by free radicals and a promising potential drug in chronic disease models in which immunopathogenicity involves high levels of RONS.

}, keywords = {Bauhinia ungulata; RAW 264.7 cells; Lipopolysaccharide; Free radicals; Antioxidant activity}, doi = {10.5530/pj.2019.1.7}, author = {Raphael de Oliveira Rodrigues and Juliana Navarro Ueda Yaochite and Milena Aguiar Braga and Amanda Ribeiro de and Sousa and Greyce Luri Sasahara and Said Gon{\c c}alves da Cruz Fonseca and Thiago Dias de Vasconcelos Ara{\'u}jo and Gilvandete and Maria Pinheiro Santiago and Le{\^o}ncio Mesquita de Sousa and Jarbas Lima de Carvalho and Francisca Bruna Stefany Aires and do Nascimento and H{\'e}lio Vitoriano Nobre J{\'u}nior and Aparecida Tiemi Nagao-Dias} } @article {1004, title = {Antiplasmodial Activity of Ethanolic Extract of Macaranga Gigantea Leaf and Its Major Constituent}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {October 2019}, pages = {1181-1188}, type = {Original Article}, chapter = {1181}, abstract = {

Introduction: This research main goal is to study the antiplasmodial activity of Macaranga gigantea leaf ethanolic extract and its major components on malaria parasites using ex vivo model. Methods: This study was conducted by extraction of M. gigantea leaves using ethanol and isolation of its major constituent. The extract and isolate were tested ex vivo on Balb-C mice{\textquoteright}s blood after i.p. administration of Plasmodium berghei strain ANKA. Antiplasmodial activity was observed from mice blood treated by various concentration of either extract or isolate and the parasitaemia percentage were determined by calculating infected blood cell after 24 h of the treatment. It is expressed as decreased of parasitaemia levels and percent of inhibition. Qualitative analysis of active fraction were tested by HPLC method. Chemical structure of isolate were characterized by using UV, IR, 1H-NMR, 13C-NMR and MS spectrophotometry. Results: Ex vivo antiplasmodial study gave the percent inhibition as much as 92.1; 85.7; 64.1; 41.5 and 21.7\% at extract concentrations of 300, 100, 30, 10 and 3 μg/ mL respectively. The IC50 values of the extract was 27.1 μg/ml. With respect to the percent of inhibition, at the same concentration, the isolate showed activity as much as 70.2; 62.5; 39.1; 21.7 and 10.8\%. The IC50 value of the isolate was 60.2 μg/ml. At the same concentration with extract and Isolate, Pyrimethamine as positive control gave percent inhibition of 94; 87.5; 44.8; 15.; and 12\%, with IC50 of 31.4 μg/ml. The results showed that major constituent of M. gigantea leaves is flavonoid. HPLC analysis using a photo diode-array detector showed that the active fraction have same retention time with that of apigenin as standard. Based on instrumental analysis data and compared with literature, a flavonoid derivate known as apigenin can be said has been isolated. Conclusion: It can be concluded that either M. gigantea leaves extract or isolated active constituent known as apigenin have potent antiplasmodial property.

}, keywords = {Antiplasmodial, Ex vivo, Flavonoid, Macaranga gigantea, Plasmodium berghei}, doi = {10.5530/pj.2019.11.183}, author = {Muhaimin Muhaimin and Yusnaidar Yusnaidar and Wilda Syahri and Madyawati Latief and Riski Dwimalida Putri and Andita Utami and Anis Yohana Chaerunisaa and Andreas Yoga Aditama and Josephine Elizabeth Siregar} } @article {1046, title = {Azadirachta indica: Antibacterial Activity of Neem Against Different Strains of Bacteria and their Active Constituents as Preventive in Various Diseases}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {November 2019}, pages = {1597-1604}, type = {Review Article }, chapter = {1597}, abstract = {

Neem has become valuable plant in the world which shows the solutions for hundreds to thousands problems. Azadirachta indica (Neem) is a rapidly growing evergreen well known tree found Pada generally in various regions of world like America, Africa and India. It has been widely used in Chinese, Ayurveda and Unani medicines across the world especially in Asians countries for the prevention and treatment of diseases. The different parts of neem plant contain biological compounds responsible for antibacterial, antiviral and antifungal activities. It is considered as safe medicinal plants and modulates the numerous biological processes without any adverse effect. Neem tree produces some active compounds which contain biological activities, parts of neem tree such as Root, bark, leaf, flower, seed and fruit together possesses biological activities. Various compounds have been obtained from various parts of neem. Biological activities of few of them have been studied. Hence, the article is aims to utilize the medicinal properties of whole neem plant in various disorders of mankind.

}, keywords = {Antibacterial, Antifungal, Azadirachta indica, Natural antibiotics, Natural products}, doi = {10.5530/pj.2019.11.244}, author = {Oscar Herrera-Calderon and Kainat Ejaz and Mahnoor Wajid and Muzzamil Shehzad and Johnny Aldo Tinco-Jayo and Edwin Enciso-Roca and C{\'e}sar Franco-Quino and Ricardo {\'A}ngel Yuli-Posadas and Victor Chumpitaz-Cerrate} } @article {1048, title = {Betel Leaf Extract Amends Dehydroepiandrosterone Induced PCOS Related Hormonal Abnormality and Histopathological Alterations in Rat Model}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {November 2019}, pages = {1442-1448}, type = {Original Article}, chapter = {1442}, abstract = {

Introduction: PCOS is a hormonal disorder with missed or irregular periods at the reproductive ages of women, which was mainly due to increased androgen levels. Objective: To evaluate the antiandrogen activity of EEBL (ethanolic extract of betel leaf) in DHEA induced PCOS (polycystic ovary syndrome) and improving ovulation rate, consequently its effects on hormonal and biochemical profile of the blood serum and Histopathology of the ovary. Methods: Divide the 30 immature (4-week-old) female Sprague Dawley rats into 5 groups. Four groups except the control group were injected each morning with dehydroepiandrosterone (DHEA) (6 mg/100 g body weight/0.2 ml sesame oil) for 20days. The control group was injected with 0.2ml sesame oil for 20days. Pretreatment completed after 21st day then animals are subjected to posttreatment with EEBL (LD-100, HD-200mg/kg, p.o) and CC (100 μg/kg, p.o) from 21 to 41 days. After the treatment animals are subjected to biochemical, hormonal and histopathological examinations. Results: In negative control group SOD, Catalase were decreased. Total protein, SGOT, SGPT, TG, LDL and cholesterol levels were increased than the control group. Hormones LH and Testosterone levels increased. FSH, estradiol, and progesterone levels were decreased when compared with the control group. Histopathology has revealed that the presence of cysts in the negative control group and recovery of cysts seen in treatment groups. Conclusion: Treatment with EEBL is effectively attenuated to the DHEA induced PCOS and it is significant in comparison results with clomiphene citrate attributing its therapeutic potential towards the treatment of PCOS.

}, keywords = {Anti-androgenic activity, Betel Leaf, Clomiphene citrate, DHEA, PCOS, Rats}, doi = {10.5530/pj.2019.11.223}, author = {K Sunand and Mahipal Yellow and P Naveen and Yasho Deepika and G Krishna Mohan and Vasudha Bakshi} } @article {932, title = {Effect of Diallyl Disulphide (DADS) on Gluconeogenesis: A Study in Isolated Alloxan Induced Diabetic Liver}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {777-781}, type = {Original Article}, chapter = {777}, abstract = {

Background: Coordinated regulation between cellular glucose uptake and endogenous glucose production is indispensable for maintenance of constant blood glucose concentrations. Liver contributes significantly by altering levels of hepatic glucose release, through controlling gluconeogenesis. Objective: To assess effect of Diallyldisulphide on hepatic gluconeogenesis by assessing gluconeogenic substrates and activity of regulatory enzyme glucose-6-phosphatase and to compare the Diallyldisulphide effect on gluconeogenesis with Metformin. Methodology: Wistar albino rats were categorized into four groups; group Inormal control. Group II, III and IV rats were administered single intraperitoneal injection of alloxan monohydrate 150 mg/kg body weight. Rats were maintained on rat diet and water adlibitum for 30 days. On 31st day rats were sacrificed and procured liver tissues. Each liver tissue cut into small slices and group-III and group-IV liver tissues were separately incubated with Diallyldisulphide 4 mg/g liver tissues and Metformin 4 mg/g liver tissues for 60 minutes at 37oC. The total amino acids and total keto acids levels were estimated after exposure. And post exposure effect on activity of glucose -6-phoshatase and transaminases were also estimated. Results: Alloxan induced diabetes resulted significant raise in total amino acids, total ketoacids, glucose -6-phosphatase and transaminases activities. Whereas incubation of liver tissues with diallyldisulphide significantly reduced total amino acids, total ketoacids, glucose-6-phosphatase, transaminases activities and ratio of total amino acids and ketoacids as compared to diabetic control rat liver tissues. Conclusion: Study suggested that diallyldisulphide suppressed gluconeogenesis as liver glucose-6-phosphatase activity is significantly decreased and precursors for gluconeogenesis were significantly reduced. Suggesting Diallyldisulphide has role in gluconeogenesis and can hold potentials for glucose homeostasis.

}, keywords = {Alloxan, Diabetes mellitus, Diallyldisulphide, Gluconeogenesis, Glucose-6-phosphatase, Total amino acid, Total keto acid}, doi = {10.5530/pj.2019.11.123}, author = {Prashanth kumar Goudappala and Ethirajan Sukumar and C V Yogaraje-Gowda and Kashinath RT} } @article {1038, title = {Effect of Fibroblast Growth Factor Combination with Ethanol Extract of Morinda citrifolia L. on Blood Glucose Levels}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {November 2019}, pages = {1558-1562}, type = {Research Article}, chapter = {1558}, abstract = {

A research has been conducted on the effect of giving Fibroblast Growth Factor (FGF) with Morinda citrifolia L. ethanol extract. This study aims to determine whether the administration of a combination of FGF with ethanol extract of noni fruit can reduce blood glucose levels in diabetes mice induced by alloxan. FGF requires amino acids in regenerating pancreatic β cells, where the amino acids expected from noni fruit can provide a signal response in regenerating pancreatic β cells. In addition, the active substances contained in noni fruit namely xeronine and flavonoid alkaloids can function to reduce blood glucose levels. Test animals were divided into 6 groups, each group consisted of 10 male white mice. Group 1 is a normal control group is a group without any given. Group 2 was a negative control group given 150 mg/kg alloxan. Group 3, 4, and 5 are the treatment groups that are given alloxan and the combination of noni fruit ethanol extract with 3 variations of dose (125; 350; and 1000) mg / KgBW plus FGF dose of 800 mg / kgBW, group 6 is the comparison which is only given FGF alone at a dose of 800 mg / kgBW. The study was conducted for 21 days, observed every 7th, 14th, 21st day using the Easy Touch{\textregistered}\ GCU digital device. The results of this study showed that administration of noni fruit ethanol extract with FGF was able to reduce blood glucose levels by significance (p \<0.05) and based on the percentage calculation of blood glucose levels as much as 44.9\% at a dose of 1000 mg / kgBW on the day observations 21st.

}, keywords = {Diabetes mellitus, FGF, Morinda citrifolia}, doi = {10.5530/pj.2019.11.238}, author = {Dharma S and Rahmawati Y and Nessa and Dillasamolla S} } @article {1037, title = {Effect of Sacha Inchi Oil (Plukenetia volubilis L.) on Genotoxicity in Mice (Mus musculus) and Subchronic Toxicity in Goldfish (Carassius auratus)}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {November 2019}, pages = {1549-1557}, type = {Research Article}, chapter = {1549}, abstract = {

Introduction: Plukenetia volubilis is known as Sacha Inchi (SI) is originary from the peruvian amazone and it has been cultivated and consumed since the pre and Inca{\textquoteright}s time. Objective: Sacha inchi oil was assessed for genotoxicity in Balb C albino mice and subchronic toxicity in goldfish (Carassius auratus). Material and Methods: The genotoxicity was assessed in Mus musculus Balb C (n = 25) separated into five groups randomly selected of twenty-five each one. Groups were 10 mL / kg normal saline (NS), 40 mg / kg cyclophosphamide group (CP) and the three other groups received cyclophosphamide and sacha inchi oil of concentrations 10, 100 and 1000 mg / kg respectively. The substances were administered three times during 24 hours. The genotoxicity in mice was evaluated determining micronucleus levels in blood and bone marrow. The subchronic toxicity was assessed in goldfish (Carassius auratus) (n = 48) separated into four groups randomly selected of six each: normal saline group (control) and three groups that received doses of 10, 100 and 1000 μg sacha inchi oil per litre of water respectively for 45 days. Results: The values of weight, length, growth rate, condition factor (K) and number of survivors were recorded. CP group showed higher micronuclei levels in blood and bone marrow compared with sacha inchi oil 10, 100 and 1000 mg / kg groups (ANOVA Test p \<0.01 Scheffe{\textasciiacute}s Post Hoc p \<0.05, p \<0.01 and p \<0.001 respectively). The subchronic toxicity assessment in goldfish showed isometric growth, a decline in "K" and a similar specific percentage growth rate per day in all groups (ANOVA test p\> 0.05). Conclusion: Sacha inchi oil was not toxic under experimental conditions.

}, keywords = {Genotoxicity, Plukenetia Volubilis, Sacha Inchi Oil, Subchronic Toxicity}, doi = {10.5530/pj.2019.11.237}, author = {Oscar Herrera-Calderon and Jorge Luis Arroyo-Acevedo and Roberto Ch{\'a}vez-Asmat and Juan Pedro Rojas-Armas and Edwin Enciso-Roca and Victor Chumpitaz Cerrate and C{\'e}sar Franco-Quino and Luz Chacaltana-Ramos and Ricardo {\'A}ngel Yuli-Posadas} } @article {1002, title = {Establishment of a 3D-structure Database for Chemical Compounds in Indonesian Sponges}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {October 2019}, pages = {1211-1218}, type = {Original Article}, chapter = {1211}, abstract = {

Objective: Nowadays, There hasn{\textquoteright}t any three-dimensional (3D) chemical structure database yet for biologically active compound in sponges from Indonesian origin. Therefore, this study aimed to create in silico a 3D-structure database of such compound and to evaluate the preferred software for this purpose. Methods: 2D- structure of selected compounds was established using MarvinSketch software. Conversion from 2D- into 3D-structures was evaluated by comparing MarvinSketch, OpenBabel and VegaZZ software packages. Visualization of the respective 3D-structures was perfomed by using PyMOL software. From 68 scientific articles, 212 chemical compounds were selected from 53 Indonesian sponge species. Results: The conversion of 2D-structures of the selected 212 chemical compound into 3D-structures lead to 7118 files, respectively consisting of 2508 files from the MarvinSketch, 1672 files from the OpenBabel and 1051 files from the VegaZZ software. The results based on the extention files were 1043 SDF, 1258 MOL and 2930 PDB format files of the three-dimensional structure. The valid and correct three-dimensional structure of chemical compound were 914 .sdf format files, 916 format .mol files and 72 .pdb format files. From the three-dimensional structures visualization, the database prefers established by using MarvinSketch with SDF or MOL format files since the results is consistent to literature and contain less number of errors.

}, keywords = {2D-and 3D-chemical structures, 3D-database of chemical structures, Evaluation of software packages, Indonesian sponges}, doi = {10.5530/pj.2019.11.188}, author = {Retno Prihatiningtyas and Rezi Riadhi Syahdi and Masteria Yunovilsa Putra and Arry Yanuar} } @article {1001, title = {HerbalDB 2.0: Optimization of Construction of Three-Dimensional Chemical Compound Structures to Update Indonesian Medicinal Plant Database}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {October 2019}, pages = {1189-1194}, type = {Original Article}, chapter = {1189}, abstract = {

Objective: Development of novel drugs is an important challenge in the pharmaceutical world and industry. In-silico methods are often considered in refinement / correction processes of drug design because they may lower the costs. The in-silico drug discovery process requires a three- Dimensional Structure (3DS) of the chemical compounds as input. Computational 3DSs often exhibit structural mismatches thus affecting the validity of the in-silico drug design process. In a previous study, a 3DS database with 1405 of Indonesian herbal compounds was developed, named HerbalDB. In this database, various structural mismatches were identified in some of the 3DSs. Our study aimed to identify and correct the structural mismatches in the herbalDB and to determine the best method in creating correct 3DS of chemical compounds. Methods: Structural mismatches in the herbal database were identified by molecular visualization. Results: The identification process yielded 170 compounds with structural mismatches that were corrected with 10 different parameters using the MarvinSketch and VegaZZ software, evaluated by molecular visualization. Conclusions: based on 3DS of chemical compound visualization, *.mol and *.sdf file format created using Dreiding force fields of MarvinSketch are the best method to construct the proper structure of Indonesian medicinal plant{\textquoteright}s chemical compound database compared with MMFF94, AMBER and CHARMM forcefields.

}, keywords = {Herbal database, MarvinSketch, Three-dimensional structure, VegaZZ}, doi = {10.5530/pj.2019.11.184}, author = {Rezi Riadhi Syahdi and Jasmine Tiara Iqbal and Abdul Munim and Arry Yanuar} } @article {1042, title = {Immunomodulator Activity of Ethanol Extract of Tapak Liman Leaves (Elephantopus scaber Linn.)}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {November 2019}, pages = {1419-1427}, type = {Original Article}, chapter = {1419}, abstract = {

Introduction: Tapak Liman (Elephantopus scaber Linn) is a medicinal plant in Indonesia which traditionally used as a treatment for fever, gout, dysentery, hepatitis, and infections. Aim: This study aims to determine the immunostimulants activity of tapak liman extract with carbon clearance method and to determine the percentage and total leukocytes and relative lymph weights. Materials and Methods: Twenty white male mice divide assigned to 1 control group and 3 experimental groups. It treated by oral administration of tapak liman extract; 10, 30, and 100 mg/kgBW. After six days of administration, mice intravenously injected with 0.1 ml/10gBW colloidal carbon. Blood obtained from the mice tail at; 3rd, 6th, 9th, 12th and 15th minutes. The determined absorbance then calculated to obtain the phagocytotic index, the percentage and the total of leukocyte cells and lymph weights. Results: Phagocytosis index increased significantly at 1, 12, 1.24 and 1.47. The percentages of neutrophil segment are 57\%, 60\% and 60\%, for lymphocytes are 3, 80\%, 32.80\% and 34.20\%, monocyte cells are 4.60\%, 3.00\% and 2.60\%, neutrophil are 3.40\%, 3.20\%,2.20\%, and for the eosinophil cells are 3.20\%, 1.8\% and 1.20\%. Total leukocyte cells are 10,760, 11,630 and 15,880 cells/microliter. The relative lymph weight of each dose in the sequence is 0.36, 0.49 and 0.66. Conclusion: Ethanol extract of tapak liman leaves (Elephantopus scaber Linn) can increase the immunity of mice.

}, keywords = {Carbon clearance, Elephantopus scaber Linn., Immunomodulator, Leucocytes, Lymph}, doi = {10.5530/pj.2019.11.220}, author = {Yufri Aldi and Dwisari Dillasamola and Gita Rahma Yanti} } @article {996, title = {In silico Analysis of Flavonoid Glycosides and its Aglycones as Reverse Transcriptase Inhibitor}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {October 2019}, pages = {1252-1255}, type = {Original Article}, chapter = {1252}, abstract = {

Background: HIV continues to be a major global public health issue, having claimed more than 35 million lives so far. In 2016, 1 million people died from HIV-related causes globally. HIV-1 reverse transcriptase is one of HIV{\textquoteright}s vital enzymes for virus reproduction. If the enzyme is inhibited, the virus multiplication could be significantly decreased. There are currently many treatments for HIV, but more effective treatment is always needed because of the possibility of drug resistance and side effects for long-term use. Based on the previous study, there are some natural compounds with high affinity to the HIV-1 reverse transcriptase enzyme. Some of these compounds are flavonoid glycosides. Aims and Method: This study was aimed to learn more about in silico HIV-1 reverse transcriptase inhibitory activities of flavonoid glycosides using docking method. Results: The results showed that the most recommended flavonoid glycosides are those with the lowest binding energy, which were kaempferol-3-O-rhamnoside, myricetin-3-O-rhamnoside and quercetin-3-O-rhamnoside. This was due to the interactions of all three flavonoid rings and sugar moiety with key amino acid residues, which were Leu100, Lys101, Glu138, Tyr181, His235 and Tyr318. Conclusion: Flavonoid glycosides with rhamnose as glycone showed lower binding energy on HIV-1 reverse transcriptase.

}, keywords = {Flavonoid, Glycosides, HIV, Molecular docking, Reverse transcriptase}, doi = {10.5530/pj.2019.11.194}, author = {Stefandi J Wijaya and Arry Yanuar and Rosita Handayani and Rezi Riadhi Syahdi} } @article {931, title = {Isolation of Oxoaphorpine Alkaloid from Bark of Cryptocarya Ferrea}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {782-786}, type = {Original Research Study}, chapter = {782}, abstract = {

Extraction, isolation, identification and characterization of the compounds isolated from the bark of Cryptocarya ferrea yielded three known oxoaphorpine alkaloids. They are o-metilmoschatoline 1, ateroline 2 and subsesiline 3. Structural elucidation was established through spectroscopic methods 1D-NMR and 2D-NMR, UV, IR, and Mass Spectrometry and comparison with the published data.

}, keywords = {Atheroline, Cryptocarya ferrea, O-moschatoline, Subsessiline}, doi = {10.5530/pj.2019.11.124}, author = {Nurdin Saidi and Khalijah Awang and Mustanir Yahya} } @article {1059, title = {Neuroprotective Effect of Sacha Inchi Oil (Plukenetia volubilis L.) in an Experimental Model of Epilepsy}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {November 2019}, pages = {1591-1596}, type = {Research Article}, chapter = {1591}, abstract = {

Background: Experimental studies have demonstrated that fatty acids such as omega 3 and 6 have anti-inflammatory, anticonvulsant, cardio protective and anti-tumor effects. Objective: The main objective was to determine the protective effect of sacha inchi oil on pentylenetetrazoleinduced seizures in albino mice. Material and Methods: Thirty male Balb/C albino mice of 8 weeks of age were purchased from the National Institute of Health (Lima-Peru). The animals were divided into 5 groups of 6 animals each one. Group I: Control; PTZ (pentylenetetrazole 80 mg / kg, s.c.). II: PTZ + Diazepam (1 mg / kg; s.c.). Group III, IV, V: PTZ + sacha inchi oil at single doses of 250, 500, 1000 mg / kg respectively orally. Sacha inchi oil was administered 30 minutes before induction of seizures by PTZ. Next, various parameters such as latency, seizure frequency, duration and score were scored according to Racine scale. The program Graph Pad Prism v.4 was used for statistical analysis. Results: As result, the experimental group treated with sacha inchi oil at maximum dose of 1000 mg/kg showed better results in response to PTZ induced seizure; low levels of seizures, frequency and duration (P\<0.001; ANOVA, P \<0.001 Post-hoc Dunnett test). Conclusion: It is concluded that Sacha inchi oil presented anticonvulsant effect at the highest doses tested being very similar to Diazepam. The main mechanism could be by reducing free radical and improving GABA levels in the brain.

}, keywords = {Convulsion, Epilepsy, Omega, Pentylenetetrazole, Plukenetia Volubilis, Sacha inchi}, doi = {10.5530/pj.2019.11.243}, author = {Oscar Herrera-Calderon and Ricardo {\'A}ngel Yuli-Posadas and Johnny Aldo Tinco-Jayo and Edwin Enciso-Roca and C{\'e}sar Franco-Quino and Victor Chumpitaz-Cerrate and Linder Figueroa-Salvador} } @article {987, title = {Phytosomal Nanoparticles Preparation of Curcuminoids to Enhance Cellular Uptake of Curcuminoids on Breast Cancer Cell Line MCF-7}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {1037-1045}, type = {Original Article}, chapter = {1037}, abstract = {

Objective: Curcuminoids, the bioactive compounds extracted from Curcuma longa consisting of Curcumin (CUR), demethoxycurcumin (DMC) and bisdemethoxycurcumin (BDMC), have shown promising biological effects, including anticancer activity. This study sought to prepare a physically stable phytosomal nanoparticles of curcuminoids (Curs-Phyto) to facilitate uptake of curcuminoids on breast cancer cells line, and further increase the cytotoxicity against cancer cells. Methods: The evaporation combined extrusion technique was employed to prepare phytosomal curcuminoids nanoparticles. The interaction between curcuminoids and phospholipid by a hydrogen bond was confirmed by differential scanning calorimetry (DSC), powder X-ray diffraction (XRD), fourier transform infrared (FT-IR), and 1H nuclear magnetic resonance (1H-NMR). Their physicochemical characterizations and stability in simulated gastric and intestinal media were investigated. The effects of Curs-Phyto on MCF-7 cells were evaluated by flow cytometry, MTS assay and cell cycle analysis. Results: We found that the Curs-Phyto were formed at a spherical shape with good size (~ 180 nm), a narrow size distribution (PDI \< d0.2), high complexation rate (~ 87\%, 95\%, and 90\% for BDMC, DMC, and CUR respectively) and high loading capacity of curcuminoids. More importantly, the Curs-Phyto showed the increased cellular uptake and enhanced cytotoxicity against MCF- 7 cancer cells, compared to free curcuminoids. Conclusion: These results indicated that the phytosome could be a promising oral delivery system for curcuminoids for cancer treatment.

}, keywords = {Cellular uptake, Curcuminoids, FACS analysis, Nanoparticle, Phytosome}, doi = {10.5530/pj.2019.11.163}, author = {Nguyen Van Long and Bui Thi Thu Ha and Anh Vu Tuan and Hoang Van Luong and Nguyen Tung Linh and Thanh Chu Duc and Phung Cao Dai and Chul Soon Yong and Chu Van Men} } @article {954, title = {The Prevalence, Attitude and Awareness of Herbal Medicine Products Use Among Pharmacy Practitioner in Jordan}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {1082-1087}, type = {Research Article}, chapter = {1082}, abstract = {

Background: There has been a universal increase in the use of herbal medicine products (HMPs). Herbal medicine considered to be the oldest form of healing and treating different diseases. Objective: The aim of this study is to determine the prevalence, attitude of HMPs use and awareness among pharmaceutical practitioner in Jordan. Methods: A descriptive cross-sectional survey was conducted using a self-administered questionnaire on a sample of 230 Jordanian pharmacy practitioner (pharmacist and pharmacy assistant), within 90 different private pharmacies in different cities of Jordan during the period of 6 months in the mid of 2018. The survey questionnaire included: the socio-demographic characteristics of participants, the source of information of the use of the HMPs, the attitude towards the use and safety of the HMPs and their combination with conventional drugs. Results: Out of 230 pharmacy practitioners interviewed in this study, the utilization rate of the HMPs use was just 41.7\%. A large number of practitioners (58.3\%) preferred conventional medicine because they believed that conventional medicine had better efficacy and better feedback than herbal products. A significant difference between pharmacist participants knowledge and work experience for more than 7 years (p-value=0.002). Majority of the participants (88.9\%) reported that they had a narrow background about the safety of these products and hadn{\textquoteright}t satisfied information regarding herb-drug interaction. Conclusion: This study counteracts other studies reported in Jordan, the usage of herbal medicine products among pharmacy practitioners isn{\textquoteright}t prevalent and isn{\textquoteright}t disseminated. They had fair information{\textquoteright}s about the usage of the herbal products especially between the pharmacist, but they were less awareness about side effects and interactions of these products. It is crucial to refresh pharmacy practitioner knowledge periodically and enhance their information by arranging different programs focused on the rational use of these products, side effects and interactions by Jordanian pharmacist association, which had a potential role in this field. In addition, they must use reliable sources for information on herbal products in order to provide desired pharmaceutical care

}, keywords = {Conventional medicines, Herbal medicine products (HMPs), Pharmacy practitioner}, doi = {10.5530/pj.2019.11.169}, author = {Noha Abd Kareem Younis Younis} } @article {797, title = {Reversible Hepatotoxicity of Cassytha filiformis Extract: Experimental Study on Liver Function and Propofol-Induced Sleep in Mice}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {January 2019}, pages = {69-74}, type = {Original Article}, chapter = {69}, abstract = {

Objective: To study the liver toxicity of Cassytha filiformis L. extract and its reversibility in mice. Methods: A total of 108 male mice were used to investigate the hepatotoxicity of Cassytha filiformis extract (CFE) and the reversibility of its toxicity to the liver. Seventy-two mice were treated with CFE orally for 7 consecutive days. A half of these animals were used to study the sleep time on propofol-induced sleep that comprised the sleep onset time (SOT) and duration of sleep (DOS), while another half was used for the quantitation of serum alanine transaminase (ALT) activity. To investigate the reversibility of the liver toxicity, thirty-six mice were treated with daily CFE for 7 days. Activities of ALT and alkaline phosphatase (ALP) were determined and the liver weight ratio was measured on day 0, 1, 3 and 7 after the termination of the CFE treatment. Data of liver toxicity determination were analyzed by two-way ANOVA followed by Duncan{\textquoteright}s multiple range test, while data of the reversibility was analyzed by Pearson{\textquoteright}s correlation. The significance level was taken at 95\% of confidence interval. Results: CFE shortened the SOT and prolonged the DOS significantly compared with control (p\<0.05). The activity of ALT was increased due to the toxicity of CFE. However, the ALT/ALP activities decreased and liver weight ratio increased gradually after the extract treatment was discontinued. The trend of these data was correlated significantly (p\<0.05). Conclusion: Cassytha filiformis L. extract is toxic to the liver but the toxicity is reversible depending on doses.

}, keywords = {Cassytha filiformis, Liver function, Propofol, Reversible toxicity, Sleep time}, doi = {10.5530/pj.2019.1.13}, author = {Yori Yuliandra and Armenia Armenia and Rahmad Arief and Mifta Hul Jannah and Helmi Arifin} } @article {951, title = {Validation of High-Performance Liquid Chromatography for Determination of Bromelain in Pineapple (Ananas comosus (L) Merr) Water}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {901-906}, type = {Original Article}, chapter = {901}, abstract = {

Objective: The aim of the present study was to validate HPLC method for analysis bromelain levels in pineapple water and application that method to determine the storage time of pineapple water. Methods: The reversed phase of HPLC method was tested and optimized before it is validated. The composition and the flow rate of the mobile phase is the optimized parameter. The analytical parameters validated were detection limits, linearity, accuracy and precision. Pineapple water was stored for 8 h at 10{\textordmasculine}C and bromelain was determined using the validated HPLC method. Result: The optimum mobile phase composition was methanolwater (70:30) with a flow rate of 1 ml/min. The detector concentration-response was linear with coefficient of determination of 0.993. The accuracy of HPLC method at a recovery of 1 and 2\% bromelain was 106.37 {\textpm} 1.94\% and 98.12 {\textpm} 1.29\% (n = 5), respectively. The precision, expressed as the coefficients of variation (CV), at 1 and 2\% bromelain were 1.83 and 1.32\% (n = 5), respectively. Bromelain level at zero time was 81.53\%. After storage for 8 h at 10{\textordmasculine}C, bromelain levels in pineapple juice appeared to decrease not statistically significant (p \> 0.05), with to mean value of 78.46 {\textpm} 2.88\%. Conclusion: The HPLC method developed was valid to analyze accurately concentrations of bromelain in pineapple water and it can be used to study the shelf life of pineapple water based on bromelain content. The bromelain content in pineapple juice was not statistically significantly different after 8 h storage at 10{\textdegree}C.

}, keywords = {Bromelain, HPLC, Pineapple water, Storage}, doi = {10.5530/pj.2019.11.144}, author = {Novi Yantih and Alfadella Methananda and Yahdiana Harahap and Wahono Sumaryono and Lestari Rahayu} } @article {999, title = {Virtual Screening of Indonesian Herbal Database as Adenosine A2A Antagonist using AutoDock and AutoDock Vina}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {October 2019}, pages = {1219-1224}, type = {Original Article}, chapter = {1219}, abstract = {

Objective: Previous research found that Adenosine A2A antagonist allows to reduce motor fluctuations, dyskinesia, protect from neurodegenerative disorder in Parkinson{\textquoteright}s disease in the human brain which is chronic progressive of losing dopaminergic neurons. The aim of this study is to explore Indonesian herbal compounds as Adenosine A2A inhibitor using virtual screening method. Methods: In this study, virtual screening of Indonesian herbal database as Adenosine A2A inhibitor was done by AutoDock and AutoDock Vina and was validated by database from A Directory of Useful Decoys: Enhanced (DUD-E). The method was validated by Enrichment Factor (EF) and Area Under Curve (AUC) of Receiver Operating Characteristics (ROC) curve Results: Based on the validation results, grid box that was used in virtual screening using AutoDock is 60 {\texttimes} 60 {\texttimes} 60 with EF1\% 16.5869 and AUC 0.8406. The two compounds Chitranone and 3-O-Methylcalopocarpin with binding energy -10.19 and -9.55 kcal/mol, respectively showing interaction with Adenosine A2A active site at residues ALA63, ILE66, ALA81, LEU85, PHE168, GLU169, MET177, TRP246, LEU249, ASN253 and ILE274. Conclusions:\ This study concludes that Chitranone and 3-O-Methylcalopocarpin could be proposed to be developed as Adenosine A2A antagonists.

}, keywords = {Adenosine A2A antagonist, AutoDock, Autodock vina, Indonesian herbal database, Parkinson{\textquoteright}s disease, Virtual Screening}, doi = {10.5530/pj.2019.11.189}, author = {Nabilah Nurtika Salamah and Widya Dwi Aryati and Arry Yanuar} } @article {998, title = {Virtual Screening of Indonesian Herbal Database as alpha-Amino-3- Hydroxy-5-Methyl-4 Isoxazolepropionic Acid (AMPA) Antagonist}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {October 2019}, pages = {1204-1210}, type = {Original Article}, chapter = {1204}, abstract = {

Objective: Ischemic stroke is one type of circulatory disturbance caused by blood clots that block blood flow to the brain. One of the impact of ischemia is nerve cell damage due to excitotoxicity. Inhibition of the ionotropic glutamate receptor such as the AMPA receptor, becomes an essential approach to the treatment of ischemia. This study aims to explore the possibility of an Indonesian herbal compound as an AMPA receptor antagonist. Methods: In this study, virtual screening of 2233 herbal compounds was performed by docking method using AutoDock to find the antagonist candidate of AMPA receptor from Indonesian herbal database. The virtual screening method was validated by an area under curve (AUC) of the ROC curve and enrichment factor (EF). Lipinski{\textquoteright}s Rule of Five was used to filter the screening result. Results: The validation of virtual screening result showed that AUC was 0.9385 and EF 1\% was 23.5550. The screening result of Indonesian herbal database showed top five compound sanggenol O, blazeispirol X, progesterone, nimolicinol and boeravinone F (-8.51; -8.39; -8.19; -8.17; -8.08 kcal/mol, respectively) and have interaction with TYR61 and THR91 residues of AMPA receptor. Conclusion: Five compounds of the Indonesia herbal database were shown as hits of AMPA receptor antagonist based on the docking method.

}, keywords = {AMPA receptor, AutoDock, Herbal plants, Neuroprotective, Virtual Screening}, doi = {10.5530/pj.2019.11.187}, author = {Rezi Riadhi Syahdi and Chindy Dwi Martinah and Arry Yanuar} } @article {871, title = {Virtual Screening of Indonesian Herbal Database for Discovery of Procaspase-3 Activators Using Autodock and Autodock Vina}, journal = {Pharmacognosy Journal}, volume = {xx}, year = {2019}, pages = {xx-xx}, type = {Original Article}, chapter = {xx}, abstract = {

Objective: Cancer is a disease where body cell grows abnormal, spread to every part of human body. Previous studies have found excessive expression of Procaspase-3 on cancer that must be activated to Caspase-3 to induce apoptotic in cells. Methods: Virtual screening of Indonesian Herbal Database was carried out to discover Procaspase-3 activators. This study was validated using enrichment factor (EF), receiver operating characteristics (ROC) area under curve (AUC) parameters. Among 1412 compounds were screened using Autodock and Autodock Vina software. Results: The virtual screening results using Autodock obtained the best ten compounds with binding energy -8.28 ~ -9.31 kcal/mol and Autodock Vina obtained the best ten compounds with binding energy -8.1 ~ -8.8 kcal/mol. Both virtual screening software showed two compounds in common, i.e., betulinic acid and maslinic acid. Conclusion: Betulinic acid interacts with Leu136A, Lys137A, Tyr195A and Pro201 residues in Autodock and Autodock Vina. While maslinic acid interacts with Leu136A, Lys137A and Pro201 residues in Autodock and Autodock Vina.

}, keywords = {Apoptotic, Cancer, Herbal, Procaspase-3 activator, Virtual Screening}, doi = {10.5530/pj.2019.11xx}, author = {Rezi Riadhi Syahdi and Ayu Annissa and Arry Yanuar} } @article {839, title = {Virtual Screening of Indonesian Herbal Database for Discovery of Procaspase-3 Activators Using Autodock and Autodock Vina}, journal = {Pharmacognosy Journal}, year = {2019}, pages = {xx-xx}, type = {Original Article}, chapter = {xx}, abstract = {

Objective: Cancer is a disease where body cell grows abnormal, spread to every part of human body. Previous studies have found excessive expression of Procaspase-3 on cancer that must be activated to Caspase-3 to induce apoptotic in cells. Methods: Virtual screening of Indonesian Herbal Database was carried out to discover Procaspase-3 activators. This study was validated using enrichment factor (EF), receiver operating characteristics (ROC) area under curve (AUC) parameters. Among 1412 compounds were screened using Autodock and Autodock Vina software. Results: The virtual screening results using Autodock obtained the best ten compounds with binding energy -8.28 ~ -9.31 kcal/mol and Autodock Vina obtained the best ten compounds with binding energy -8.1 ~ -8.8 kcal/mol. Both virtual screening software showed two compounds in common, i.e., betulinic acid and maslinic acid. Conclusion: Betulinic acid interacts with Leu136A, Lys137A, Tyr195A and Pro201 residues in Autodock and Autodock Vina. While maslinic acid interacts with Leu136A, Lys137A and Pro201 residues in Autodock and Autodock Vina

}, keywords = {Apoptotic, Cancer, Herbal, Procaspase-3 activator, Virtual Screening}, doi = {10.5530/pj.2017.4.x}, author = {Rezi Riadhi Syahdi, and Ayu Annissa and Arry Yanuar} } @article {631, title = {Antioxidant and Antidiabetic Potential of Galing Stem Extract (Cayratia trifolia Domin)}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {June 2018}, pages = {686-690}, type = {Original Article}, chapter = {686}, abstract = {

Galing (Cayratia trifolia Domin.) have been used empirically to treat various diseases, one of them is antidiabetic. Objective: To determine the phytochemical content and the activity of the ethanol extract of the galing stem as antioxidant and antidiabetic. Method: The galing stem extract was investigated for phytochemical by Thin Layer Chromatography (TLC) and its antioxidant activity using DPPH scavenging activity assay. In vivo, antidiabetic test was conducted by animal diabetes modeling that has given streptozotocin 150 g/kg BW and 10\% of sucrose solution intraperitoneally. The average level of fasting blood glucose at 307 mg/dL. Mice were divided into 6 groups, normal control group, diabetes induction group, positive group (treated by glibenclamide) and treatment group consisted of three groups were treated by ethanol extract of galing stem in dose 400, 500, and 600 mg/kg BW, respectively. Mice treated with appropriate doses of each treatment once a day for 7 days. The measuring blood glucose level was using a photometer 5010V5+. Results: The ethanol extract of galing stem contained the alkaloid, flavonoid, saponin, tannin, and triterpene. It is potential as an antioxidant with the IC50 61,52 mg/L which indicated that the extract had strong antioxidant. The antidiabetic activity showed that the effect of extract 400 and 500 mg/kg BW are not different significantly with glibenclamide in reducing blood glucose levels subset of the statistics ANOVA (p\> 0.05). Conclusion: The ethanol extract of galing steam is potent as an antioxidant due to the phytochemical content inside particularly the flavonoid compound.

}, keywords = {Antidiabetic, Antioxidant, Galing stem, Mice, Phytochemical}, doi = {10.5530/pj.2018.4.113}, url = {http://fulltxt.org/article/651}, author = {Muhammad Ilyas Yusuf and Wahyuni and Sri Susanty and Ruslan and Muammar Fawwaz} } @article {774, title = {Chemicals and Bioactivity Discrimination of Syconia of Seven Varieties of Ficus deltoidea Jack via ATR-IR Spectroscopic-Based Metabolomics}, journal = {Pharmacog Journal}, volume = {10}, year = {2018}, month = {November 2018}, pages = {s147-s151}, type = {Original Article}, chapter = {s147}, abstract = {

Introduction: Ficus deltoidea is one of the common Malaysian medicinal plants and currently commercialized as raw ingredients in some local food products. However, those products do not discriminate the varieties of Ficus deltoidea used. Methods: FTIR-based metabolomics coupled with chemometric technique was applied to discriminate chemical components in ethanolic extracts of syconia of seven varieties of Ficus deltoidea namely; var. deltoidea, var. trengganuensis, var. kunstleri, var. angustifolia, var. bilobata, var. intermedia and var. motleyana. Unsupervised multivariate data analysis (MVDA) including principal component analysis (PCA) was used as to evaluate chemical variability among the seven varieties. For discrimination, orthogonal partial least square discriminant analysis (OPLS-DA) was applied, while partial least square (PLS) was used to evaluate the relationship between the alpha-glucosidase inhibition, antioxidant activity and Ficus deltoidea varieties. Results: As a result, OPLS-DA successfully discriminated the seven varieties. The FTIR fingerprints which were responsible for the discrimination includes 1729, 1705, 1448, 1095, 453, 443 cm-1. In addition, PPLS model demonstrated the correlation between var. kunstleri, var. deltoidea and var. intermedia respective chemicals fingerprints and their bioactivity (DPPH, FRAP and \α-glucosidase inhibition). Conclusion: The findings revealed that FTIR spectroscopy, in combination with MVDA, can be used for structural functional discrimination in relation to the sample bioactivity.

}, keywords = {Alpha-glucosidase Inhibition, antioxidant activity, Fourier Transform Infra-red Spectroscopy, Orthogonal Partial Least Square Discriminant Analysis, Principal Component Analysis}, doi = {10.5530/pj.2018.6s.27}, author = {Alkasim Kabiru Yunusa and Zalilawati Mat Rashid and Nashriyah Mat and Che Abdullah Abu Bakar and Abdul Manaf Ali} } @article {516, title = {Evaluation of Chemoprotective Effect of Quercetin from Argyreia speciosa against N-methyl-N-Nitro-N-Nitrosoguanidine and NaCl-Induced Gastric Carcinomas in Wistar Rats}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {January 2018}, pages = {215-220}, type = {Original Article}, chapter = {215}, abstract = {

Objectives: This study was carried out to investigate the chemo protective potential of Quercetin, an isolated compound from Argyreia speciosa, on N-methyl-N-nitro-N-nitrosoguanidine and NaCl-induced gastric carcinomas in Wistar rats. Methods: The rats were fed with a diet supplemented with 8\% NaCl and simultaneously given N-methyl-N-nitro-N-nitrosoguanidine. After administration of the carcinogen, quercetin was administered. The whole stomach and a part of duodenum were sampled, cut open and tumors were recorded. The specimens were histopathologically investigated and the expression of surviving was examined with immunohistochemical analysis. Results and Conclusions: The treatment with quercetin significantly increases body weight in the rats after N-methyl-N-nitro-N-nitrosoguanidine administration. Survivin expression in glandular stomachs of normal rats, of rats in adenocarcinomas and quercetin at dose dependent manner treated rats were 0\%, 90\%, 75\%, 33.3-25\%, respectively. Compared with the survivin expression in negative rats, the differences were significant. Compared with the survivin expression in normal rats, the differences were significant. Histological observations of stomach tissues too correlated with the biochemical observations. These findings indicated that the Quercetin treatment could stimulate immunity activity in rats with N-methyl-N-nitro-N-nitrosoguanidine induced gastric carcinoma and have pronounced effect on survivin which is an attractive target for gastric cancer therapy.

}, keywords = {Argyreia speciosa, Gastric carcinoma, Immunochemistry, Quercetin}, doi = {10.5530/pj.2018.2.37}, url = {http://fulltxt.org/article/467}, author = {Lubna Azmi and Ila Shukla and Shyam Sundar Gupta and Aniruddh Chaudhary and Padam Kant and Narayan Prasad Yadav and Chandana Venkateswara Rao} } @article {632, title = {Functional and Morphological Studies of Organic and Inorganic Tomatoes}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {June 2018}, pages = {715-719}, type = {Original Article}, chapter = {715}, abstract = {

Aim: To study the functional and morphological characteristics of organic and inorganic tomatoes. Methodology: UV treated, and untreated organic and inorganic tomato powdered samples were assessed using an analytical technique FT-IR and SEM. Results: FT-IR spectra of organic control samples showed peaks at (3290.12, 2924.72 and 1611.61 cm-1) while, organic treated samples revealed some peaks at (3287.11, 2925.66 and 1612.91 cm-1), inorganic control tomatoes confirmed the peaks at (3289.47, 2925.76 and 1619.26 cm-1) and in inorganic treated tomatoes peaks was at (3289.42, 2925.34 and 1619.31 cm-1) respectively, on confirming the presence of O-H, C-H, C=C, C=O and C-OH functional groups. However, results confirmed slight changes in functional groups of organic and inorganic samples and UV treatment helps in decreasing the effect of fluoride, chloride and other synthetic chemicals level by disinfecting the samples. SEM micrographs showed non-significant changes with minimal effect of UV in all samples. Conclusion: The outcome of the study helps in effective understanding of functional and microstructural differences between organic and inorganic tomatoes.

}, keywords = {FT-IR, Inorganic, Organic, SEM, Tomatoes, UV treatment}, doi = {10.5530/pj.2018.4.119}, url = {http://fulltxt.org/article/657}, author = {Shwetha Manchanabele Shankar and Sinija Vadakkepulppara Ramachandran Nair and Manoharan Duragdevi and Binod Kumar Yadav and Shanmugasundaram Saravanan} } @article {606, title = {Functional and Morphological Studies of Organic and Inorganic Tomatoes}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {May 2018}, pages = {715-719}, type = {Original Article}, chapter = {715}, abstract = {

Aim: To study the functional and morphological characteristics of organic and inorganic tomatoes. Methodology: UV treated, and untreated organic and inorganic tomato powdered samples were assessed using an analytical technique FT-IR and SEM. Results: FT-IR spectra of organic control samples showed peaks at (3290.12, 2924.72 and 1611.61 cm-1) while, organic treated samples revealed some peaks at (3287.11, 2925.66 and 1612.91 cm-1), inorganic control tomatoes confirmed the peaks at (3289.47, 2925.76 and 1619.26 cm-1) and in inorganic treated tomatoes peaks was at (3289.42, 2925.34 and 1619.31 cm-1) respectively, on confirming the presence of O-H, C-H, C=C, C=O and C-OH functional groups. However, results confirmed slight changes in functional groups of organic and inorganic samples and UV treatment helps in decreasing the effect of fluoride, chloride and other synthetic chemicals level by disinfecting the samples. SEM micrographs showed non-significant changes with minimal effect of UV in all samples. Conclusion: The outcome of the study helps in effective understanding of functional and microstructural differences between organic and inorganic tomatoes.

}, keywords = {FT-IR, Inorganic, Organic, SEM, Tomatoes, UV treatment}, doi = {10.5530/pj.2018.4.119}, url = {http://fulltxt.org/article/657}, author = {Shwetha M S and Sinija V R and M Durgadevi and B K Yadav and S Shanmugasundaram} } @article {640, title = {Indonesian Herbal SGLT2 Inhibitor Discovery through Pharmacophore-Based Virtual Screening}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {June 2018}, pages = {803-807}, type = {Original Article}, chapter = {803}, abstract = {

Objective: Sodium-glucose cotransporter 2 (SGLT2) inhibitor had been evaluated in clinical trials as the basic strategy of hyperglycemia handling in diabetes. However, because of SGLT2 inhibitors is the new class of oral antidiabetic, it is rare to be found in Indonesia, and it is costly. This study was intended to find compounds from Indonesian herbal database that show capability to be used as SGLT2 inhibitors through a pharmacophore-based virtual screening approach. Methods: The SGLT2 inhibitor pharmacophore models were made from 10 training sets of SGLT2 ligand inhibitors using the Ligand Scout 4.1.5. Ten pharmacophore models which had been made were validated using test set and decoy set methods to know how the performance of pharmacophore model worked. Virtual screening were then applied to the best pharmacophore model. Results: The model-1 pharmacophore was the best model, with values of 0.9080, EF1\% = 56.5, EF5\% = 56.5 and AUC100\% = 0.87 which served as model for virtual screening. Model-1 consisted of one hydrophobic interaction, one aromatic ring, four hydrogen bond donors and five hydrogen bond acceptors. Virtual screening showed three compounds (Hits) with best pharmacophore fit scores according to model-1 among 1377 compounds, they were vitexin = 113.62; cucumerin A = 112.62; and cucumerin B = 113.51. Conclusion: These results showed that vitexin, cucumerin A, and cucumerin B potentially have activity as an SGLT2 inhibitor.

}, keywords = {Diabetes, Pharmacophore, SGLT2 Inhibitor, Virtual Screening}, doi = {10.5530/pj.2018.4.136}, url = {http://fulltxt.org/article/674}, author = {Rezwendy R and Rezi Riadhi Syahdi and Arry Yanuar} } @article {641, title = {Molecular Dynamic Simulation of Hydroxymethylglutaryl-CoA Reductase Inhibitors from Gnetum gnemon L. Seed Extract}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {June 2018}, pages = {793-797}, type = {Original Article}, chapter = {793}, abstract = {

Objective: Gnetum gnemon L. (melinjo) seed extract contained trans-resveratrol which has been shown to inhibit hydroxymethylglutaryl-CoA (HMG-CoA) reductase. Therefore it has a potent activity for lowering blood cholesterol. This study was carried out to determine the molecular dynamics simulation of HMG-CoA reductase inhibitors from Gnetum gnemon L. seed extract. Methods: Molecular dynamics simulation using AMBER was used. The simulation was set at 300 K as default temperature and 310 K, average human body temperature. The main parameters of this study were ligand-residue interaction, binding affinity, root mean square deviation (RMSD), root mean square fluctuation (RMSF), hydrogen bonds analysis, molecular mechanics Poisson Boltzmann surface area (MMPBSA), and molecular mechanics generalized born surface area (MMGBSA). Results: In the simulation study, trans-resveratrol, trans-piceid, gnemonol M, gnemonoside B, viniferin and gnetin C had shown lower energy than HMG (PDB ID: MAH), the substrate of HMG-CoA Reductase. Free energy binding obtained from simulation was between 11.1 to -31.38 kcal/mol. Conclusion: The simulation at 310 K was preferable than 300 K as more interactions were performed and higher affinity was obtained.

}, keywords = {Gnetum gnemon L, Hydroxymethylglutaryl-CoA reductase inhibitor, Molecular dynamics, Trans-resveratrol}, doi = {10.5530/pj.2018.4.134}, url = {http://fulltxt.org/article/672}, author = {Yuditya Artha and Arif Arrahman and Azminah and Arry Yanuar} } @article {619, title = {Neuroprotective Activity of Sesbania grandifolara Seeds Extract Against Celecoxib Induced Amnesia in Mice}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {May 2018}, pages = {747-752}, type = {Original Article}, chapter = {747}, abstract = {

Background: Sesbania grandiflora are characterized by their high anti-oxidant properties. The degeneration of neurons in Alzheimer disease mainly occurs because of high production of free radicals. However, the impact of Sesbania grandiflora on cholinergic system and oxidative stress parameter has not been investigated. Aim: The present study was designed to evaluate the neuroprotective effect of ethanolic extract of Sesbania grandiflora seeds in mice. Material and method: The seeds of Sesbania grandiflora were powdered and subjected to successive extraction in Soxhlet apparatus. The different doses of ethanolic extract of Sesbania grandiflora seeds were evaluated for its neuroprotective activity against celecoxib induced amnesia in mice. Result and Conclusion: Phytochemical analysis of various extracts of Sesbania grandiflora revealed the presence of steroid, saponin, flavonoid, tannins and phenolic compounds. The ethanolic extract of Sesbania grandiflora significantly improves the memory of mice and reestablishes the amnesia induced by celecoxib. In addition to improvement in memory the extract treatment also decreases the activity of AchE and MDA and restore the antioxidant anzyme SOD, GSH and catalase in experimental animals. The results of our study showed that ethanolic extract of Sesbania grandiflora improve the cognition dysfunction in celecoxib treated mice through the modification in cholinergic system or by the blockage of oxidative stress and inhibition of AchE enzyme.

}, keywords = {Acetylcholine, Celecoxib, Free radical, Morris water maze, Sesbania grandiflora}, doi = {10.5530/pj.2018.4.125}, url = {http://fulltxt.org/article/663}, author = {Bhupesh Chander Semwal and Madhuri Verma and Yogesh Murti and Harlokesh Narayan Yadav} } @article {583, title = {The Phythochemical Research of Armenian Apricot Gums (Gummi armeniacae)}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {March 2018}, pages = {476-479}, type = {Original Article}, chapter = {476}, abstract = {

Aim: The plant derivative, the gum\’s exudates are of great interest among polysaccharides. Nowadays, it is of crucial importance to study the structural peculiarities and the conditioned biological activity of the Gummi Armenicae of native origin as an alternative version of the Gummi Arabicae. Materials and methods: As a material for research served the gum procured from Apricot trees (Armenian Vulgaris Lam.), cultivated in different regions of Armenia annually in spring during juice motion period in 2010-2014 years. The quantity of polysaccharides in gum was determined by the method of gravimetric balance after drying. The quantitative ratio of monosaccharide in the examined polysaccharide complex was detected by the method of MRI. Results: By the methods of spectral analysis (PMR 1H and NMR 13C) the structure of Apricot gums polysaccharide fraction was detected. From the analysis of PMR 1H and NMR 13C spectra it is obvious that polysaccharide complex fraction is composed from the rest of \α- L-arabionopyranose, \β -L-arabionopyranose, \α- D-galactopyranose, \β -D-galactopyranose, \α -D-glucopyranose, \β -D-glucopyranose. Low molecular compounds in nonpolar fraction of apricot gum were determined by GC-MS method. The results show that in Rt1=22.5, Rt2=26.3, Rt3=31.4. Simple phenols were registered \– peaks of catechols{\textquoteleft} hydroquinones, pyrogallols, amounts of which are respectively 7.58\%, 4.27\%, 5.69\%.

}, keywords = {13C NMR, Apricot gum, Chemical structure, GC-MS, Simple phenols}, doi = {10.5530/pj.2018.3.78}, url = {http://fulltxt.org/article/511}, author = {Chichoyan Naira Babken and Mamyan Suren and Shaboyan Naira and Melikyan Yelena} } @article {724, title = {A Review on Phytopharmacopial Potential of Epilobium angustifolium}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1076-1078}, type = {Review Article}, chapter = {1076}, abstract = {

Nature has been a source of medicinal agents for thousands of years, and an impressive number of modern drugs have been isolated from natural sources which are based on their use in traditional medicine. Epilobium angustifolium L is a perennial herbaceous plant that belongs to the Onagraceae family. It exhibits various therapeutic properties like anticancer, antibacterial, anti-inflammatory, antioxidant, and anti-aging properties. Epilobium angustifolium L. contains polyphenols and secondary metabolites like oenothein B. Information was collected via Medline, PubMed, and Science Direct. Also some data have been collected from scientific journals, books, and reports. This review gives the current information on the chemical composition, traditional uses, and documented biological activities of Epilobium angustifolium L. These studies reveal that Epilobium angustifolium L is a source of medicinally active compounds and have various pharmacological effects. These studies will be helpful to create interest toward Epilobium angustifolium L and may be useful in developing a new direction for further research.Epilobium angustifolium L.is a medicinally important plant belongs to Onagraceae family. Extract from the plant is used in the treatment of many diseases for its anti-tumor, antimicrobial, anti-inflammatory, antioxidant, anti-ulcer and many other properties. The medicinal properties of fireweed have been attributed to its high content in polyphenols and more particularly to the most abundant of its secondary metabolites: Oenothein B.

}, keywords = {Biological activities, Epilobium angustifolium L, Herbaceous, Oenothein B, Pharmacological Effects}, doi = {10.5530/pj.2018.6.181}, author = {Prasad Kadam and Manohar Patil and Kavita Yadav} } @article {491, title = {Simultaneous Quantification of Bioactive Triterpene acids (Ursolic acid and Oleanolic acid) in Different Extracts of Eucalyptus globulus (L) by HPTLC Method}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {December 2017}, pages = {179-185}, type = {Original Article}, chapter = {179}, abstract = {

Objective: To develop a novel analytical method for simultaneous determination of two triterpenic acids by high-performance thin layer chromatography in methanol and dichloromethane extracts of Eucalyptus globulus leaf. Ursolic acid was also isolated from Eucalyptus globulus leaf. Materials and Methods: Two triterpenic acids (ursolic and oleanolic acid) were extracted using methanol and dichloromethane as the extraction solvents. Study for total triterpenoids present in Eucalyptus globulus leaves was carried out which shows considerable amount of terpenoids present. Because of the similarity of chemical structure, the prechromatographic derivatization was necessary to separate these triterpenic acids. The samples were treated by 1\% iodine solution in chloroform directly on the chromatographic plate and developed with the mobile phase consisting of petroleum ether, ethyl acetate and acetone (7.8:2.2:0.1, v/v/v). After drying, the plates were sprayed with 10\% (v/v) ethanol solution of sulfuric acid and heated to 120 \°C for 3 min. Quantification was performed in absorbance/transmittance mode at a wavelength of 345 nm. The developed HPTLC method was validated for linearity, precision and accuracy. Results: Correlation coefficient (r2 \> 0.99), R.S.D. values, detection limits as well as recovery values were found to be satisfactory. Ursolic acid was isolated from E. globulus leaves. The identification of isolated ursolic acid was done on the basis of Rf value (0.26) for HPTLC and peak interpretation for FT-IR. Conclusion: The method has been successfully applied in the analysis of both triterpenic acids in medicinal herbs.

}, keywords = {HPTLC, Iodine derivatization, Oleanolic acid, Triterpenes, Ursolic acid}, doi = {10.5530/pj.2018.1.30}, url = {http://fulltxt.org/article/416}, author = {Arti Gupta and Pooja Maheta and Renu Chauhan and Sonia Pandey and Jitendra Singh Yadav and Shailesh Shah} } @article {769, title = {Total Phenolic, Total Flavonoid, Quercetin Content and Antioxidant Activity of Standardized Extract of Moringa oleifera Leaf from Regions with Different Elevation}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {November 2018}, pages = {s104-s108}, type = {Original Article}, chapter = {s104}, abstract = {

Context: Moringa oleifera is the famous plant that has been used as medicinal plant for diverse pharmacological activity. Aims: To evaluate the total phenolic, total flavonoid, quercetin content as well as the antioxidant activity of standardized extract of Moringa oleifera (Lamk) leaf, collected from three regions with different elevation. Materials and Methods: The leaves were extracted by maceration method using ethanol 96\% and evaporated by rotary evaporator to obtain the viscous extract. The determination of total phenolic and total flavonoid were performed by spectroscopic method, while the quercetin concentration were determined by high performance liquid chromatography (HPLC). The antioxidant activity was evaluated by 2,2-diphenyl-1-picrylhydrazyl (DPPH) method. Results: Ethanolic extracts of Moringa oleifera leaf from region with medium altitude (Sigi regency) showed higher total phenolic, total flavonoid, quercetin concentration and antioxidant activity than regions with low and high altitude (Parigi and Palu cities). Conclusion: This study reveals the potency of standardized extracts of Moringa oleifera growing in medium altitude (Sigi regency) to be developed as antioxidant herbal medicine.

}, keywords = {Antioxidant, Kelor, Moringa oleifera, total flavonoid, total phenolic}, doi = {10.5530/pj.2018.6s.20}, author = {Evi Sulastri and Muhammad Sulaiman Zubair and Nurafni Israyanti Anas and Syakila Abidin and Ririen Hardani and Risfah Yulianti and Aliyah} } @article {738, title = {Virtual Screening of Indonesian Herbal Database as Murine Double Minute-2 (MDM2) Inhibitor}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1184-1189}, type = {Original Article}, chapter = {1184}, abstract = {

Background: Murine Double Minute-2 (MDM2) overexpression causes the p53 deficiency, so the role p53 as a cell regulator does not work in the case of cancer. Methods: In this study, virtual screening of Indonesian herbal database to discover MDM2 inhibitors was carried out. Autodock and Autodock Vina validated with Directory of Useful Decoy-Enhanced (DUD-E). Validation parameters were performed with Enrichment Factor, Receiver Operating Characteristics, and Area Under Curve. Results: The validation with the grid box 70x70x70 on Autodock resulting AUC value 0.72, while in Autodock Vina 0.43. Autodock Vina did not fulfilll the standard value but still used for comparison. Based on the virtual screening result, top ten compounds from Autodock are Nimolicinol, Jacoumaric acid, Isoarborinol, Lantic acid, Diosgenin, Theasaponin E1, Taraxasterol, Leucadenone C, Simiarenol, and Alpha-Amyrin were found to have strong interaction with MDM2, with binding energy (\ΔG) ranging from -8.83 to -9.65 kcal/mol. The Autodock Vina screening resulted in the identification of Yuehchukene, Morusin, Cyanidin, Leucadenone C, Roxburghine-B, Ocidentoside, Beta-sitosterol, Curine, Withangulatin, and Jacoumaric acid as potential inhibitors with binding energy (\ΔG) ranging from -8.7 to -9.4 kcal/mol. Conclusion: Jacoumaric acid and Leucadenone C were shown to interact with the active site in MDM2 at residues Leu54, Ile61, Met62, and Ile99.

}, keywords = {Cancer, Docking, Indonesian Herbal, Inhibitor, MDM2, Virtual Screening}, doi = {10.5530/pj.2018.6.203}, author = {Alexander Victory and Rezi Riadhi Syahdi and Arry Yanuar} } @article {260, title = {ACE Inhibitory Activity, Total Phenolic and Flavonoid Content of Watercress (Nasturtium officinale R. Br.) Extract}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {February 2017}, pages = {249-251}, type = {Original Article}, chapter = {249}, abstract = {

Introduction: Hypertension is the main risk factor for cardiovascular disease. There are many developed antihypertension drugs, one of them is focusing in ACE (Angiotensin Converting Enzyme) inhibition activity. ACE inhibition activity known can decrease vasoconstriction effect and also can decrease bradykinin degradation (vasodilator) by creating NO (nitric oxide). Methods: In this study, we conducted an in vitro ACE inhibition activity test which was obtained from watercress on 70\% ethanolic extract and each fraction (n-hexane, ethyl acetate, and n-butanol). Results: Results of the study showed that ethanolic extract of watercress had ACE activity with IC50 value was 19.05 g/mL and the highest IC50 of each fraction is ethyl acetate with IC50 value was 2,303 g/ mL. n-butanol fraction had the highest total phenolic content with 15.798 mg GAE/g of the extract, while the highest total flavonoid content was obtained on ethyl acetate fraction with 82.847 mg QE/g of the extract. Conclusion: The results suggest that Watercress (Nasturtium officinale R. Br.) possess ACE inhibitory activity.

}, keywords = {ACE inhibitor, Flavonoid, phenolic, Watercress (Nasturtium officinale R. Br.)}, doi = {10.5530/pj.2017.2.42}, url = {http://phcogj.com/fulltext/309}, author = {Catty Amalia Yaricsha and Rissyelly and Katrin} } @article {256, title = {Application of Ionic Liquid based Microwave-Assisted Extraction of the Secondary Metabolite from Peperomia pellucida (L) Kunth}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {February 2017}, pages = {227-234}, type = {Original Article}, chapter = {227}, abstract = {

Introduction: An ionic liquid (ILs) is a new alternative solvent (containing cations and anions) has the physical and specific solutions properties, and also had proven to be a promising substituent of conventional organic solvents are flammable, volatile and toxic in various processes. The ILS application in separating the secondary metabolites compound from Peperomia pellucida (L) Kunth herbaceous can be carried out using microwaveassisted extraction method (MAE). Objective: The aim of this study was to investigate the effect of ionic liquid based microwave-assisted extraction method for attracting the secondary metabolites compound from P. pellucida compared with a conventional solvent for the enrichment of secondary metabolites (especially polyphenols group) and their HPTLC fingerprinting profile. Methods: The herb dried powder extracted by microwave-assisted extraction using an ionic liquid such us 1-Butyl-3-methylimidazolium chloride ([BMIM]Cl), 1-Butyl-3-methylimidazolium Bromide ([BMIM]Br). The obtained extract solution was partitioned using an organic solvent; the extract was evaporated to obtain a dry extract and determination the HPTLC fingerprinting profile. Results: Based on the research results was obtained from the various types of solvents there are differences in the extraction of secondary metabolite.

}, keywords = {HPTLC profile, Ionic liquid, Microwave-assisted extraction, Peperomia pellucida (L) Kunth, Secondary metabolite.}, doi = {10.5530/pj.2017.2.38}, url = {http://phcogj.com/fulltext/305}, author = {Islamudin Ahmad and Arry Yanuar and Kamarza Mulia and Abdul Mun{\textquoteright}im} } @article {258, title = {Effect of Gamma Irradiation on Suruhan (Peperomia pellucida (L.) Kunth) Herb Powder}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {February 2017}, pages = {239-243}, type = {Original Article}, chapter = {239}, abstract = {

Introduction: Peperomia pellucida (L.) Kunth is known as a raw material for herbal medicine; Preservation of herbs powder by gamma irradiation is reported to be able to keep products free from contamination. Methods: This study aims to evaluate the effect of gamma irradiation (0; 2.5; 5; 7.5; and 10 kGy) on the ACE inhibitory activity (ACE Kit \– WST test kit method), antioxidant activity (DPPH radical scavenging method), total phenolic content (colorimetric method using Folin-Ciocalteu reagent), total flavonoid content (colorimetric method using AlCl3 and sodium acetate), and TLC profiling (silica gel F254 as the stationary phase and dichlormethane:methanol [92:8] as the mobile phase) of suruhan herb powder. Results: Results showed that the 2.5 kGy irradiation dose gave the smallest alteration in ACE inhibitory activity compared to others irradiated doses. Furthermore, the 5 and 7.5 kGy dose didn\’t cause significant change (p\>0.05) on antioxidant activity, total phenolic content, and total flavonoid content. Antioxidant activity was found to correlate with the total phenolic content but not with the total flavonoid content. Conclusion: Based on these finding, it is concluded that gamma irradiation can be used as a preservation method for P. pellucida herb powder.

}, keywords = {Angiotensin converting enzyme, antioxidant activity, Peperomia pellucida, total flavonoid, total phenolic}, doi = {10.5530/pj.2017.2.40}, url = {http://phcogj.com/fulltext/307}, author = {Mubarika Sekarsari Yusuf and Intan Wulandari and Lili Amelia and Katrin and Arikadia Noviani and Rissyelly and Abdul Mun{\textquoteright}im} } @article {398, title = {HPLC Determination of Quercetin in Three Plant Drugs from Genus Sedum and Conjecture of the Best Harvest Time}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {725-728}, type = {Original Article}, chapter = {725}, abstract = {

To establish a method for quercetin content determination of the three plant drugs from genus Sedum and to decide their best harvesting time. Dried herbs of Sedum sarmentosum Bunge., S. lineare Thunb. and S. erythrostictum Migo. are all traditional medicines from Genus Sedum. They all have long been used to cure hepatitis, dysentery, swelling poison and so on. It has been reported that flavonoids contained in S. sarmentosum Bunge. were one type of the active components to protect liver and reduce serum alanine aminotransferase level. Through the qualitative analysis and TLC assay, we have verified that both S. lineare Thunb. and S. sarmentosum Bunge. contain flavonoid glycosides whose aglycones include quercetin. In this study, a HPLC methodology was established to determine quercetin which was a common hydrolyzate of the flalvonoid glycosides in the three plant medicines. The determination method developed showed good linearity in the range of 41.2-412.0 \μg/mL, and had a nice accuracy and repeatability. It indicated that the content of quercetine in Sedum sarmentosum, Sedum lineare and Sedum emarginatum can achieve the quality standard required by Chinese Pharmacopoeia.( No less than 0.01\%), The results also revealed preliminarily a relation between collected season and medicine quality. Thus it could be used to control some flavonoids content in the three plant drugs indirectly. By determining the samples of the 3 drugs collected in different seasons, the optimal harvest periods could be preliminarily ascertained.

}, keywords = {best harvest time., Genus Sedum, HPLC determination, Plant medicines, Quercetin}, doi = {10.5530/pj.2017.6.114}, url = {http://fulltxt.org/article/167}, author = {Ma Yue-ling and Chen Yu-jie and Wan Ding-rong and Chen ping and Xu Ran} } @article {415, title = {Hypoglycemic and Hypolipidemic Activities of Ethanolic Extract from Mimosa pudica L. in Normal and Streptozotocin-Induced Diabetic Rats}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {834-837}, type = {Original Article}, chapter = {834}, abstract = {

Context: Mimosa pudica L. its unique property to collapse when touched and opens up. Aims: To evaluate hypoglycemic and hypolipidemic activities of 80\% ethanolic extract from whole plant of Mimosa pudica L. (MPE) by measuring fasting blood glucose in normal and streptozotocin (STZ)-induced diabetic rats treated with MPE. Materials and Methods: An eight-week study using MPE was performed in normal and streptozotocin (STZ)-induced diabetic rats. Hypoglycemic activities in normal and STZ-induced diabetic rats and oral glucose tolerance test (OGTT) and biochemical data include total cholesterol (TC), triglycerides (TG), high-density lipoprotein (HDL) and low-density lipoprotein (LDL) of MPE were compared with glibenclamide, a standard anti-diabetic drug. Results: OGTT showed that MPE did not decrease blood glucose both in normal and STZ-induced diabetic rats comparable to controls and glibenclamide treated rats. Moreover, MPE did not affect FBG in the normal rats. However, it significantly (p\<0.05) decreased FBG in the diabetic rats while MPE increased HDL and decreased TC, TG and LDL in the diabetic rats. Conclusions: The results from this study confirmed the traditional use of Mimosa pudica L. for the treatment of diabetes mellitus.

}, keywords = {Hypoglycemic, Hypolipidemic, Mimosa pudica, Oral glucose tolerance test.}, doi = {10.5530/pj.2017.6.130}, url = {http://fulltxt.org/article/183}, author = {Piyapong Yupparach and Ampa Konsue} } @article {414, title = {Phenolic Constituents, Anti-Inflammatory and Antidiabetic Activities of Cyperus laevigatus L.}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {828-833}, type = {Original Article}, chapter = {828}, abstract = {

Background: Cyperus species are well known traditional plants and used for several diseases around the world. Aim of the Study: Our study aimed to identification of the phenolic constituents in addition to evaluation of different extracts of Cyperus laevigatus L as antioxidant, antiinflammatory and antidiabetic agents. Materials and Methods: The phenolic constituents were identified using spectroscopic techniques. The antioxidant activity was evaluated using in vitro DPPH assay. Total extract, methanol and EtOAc fractions were evaluated for their antiinflammatory activity using RAW 264.7 macrophages assay. Antidiabetic activity of the total extract was examined biochemically and histopathologically using streptozotocin-induced diabetic rats. Results: A new flavone, chrysoeriol 7-O-\β-(6'''-O-acetyl-\β-D-glucopyranosyl)-(1\→4) glucopyranoside (1), along with seven knowns (2-8) were isolated from Cyperus laevigatus L. The structures of isolated compounds were established depending upon 1D, 2D-NMR and HR-ESI-MS. The MeOH and EtOAc fractions exhibited significant antioxidant activity while the isolated flavonoids exhibited from moderate to weak antioxidant activity. The total extract, MeOH and EtOAc fractions exhibited significant anti-inflammatory activity using LPS-stimulated RAW 264.7 macrophages model by decreasing of NO accumulation by 76 \– 66\% and 84 \– 67\%, of the original accumulation values with increasing concentrations in comparison with the reference drug, dexamethasone. The total extract exhibited antidiabetic activity in streptozotocin-induced diabetic rats and this effect was manifested by decreasing serum levels of glucose, glucagon and NO. It also increased level of insulin and promoted paraoxonase activity. Conclusion: These results proved that this plant may be multiple sources for medicinal natural drugs especially for anti-inflammatory and antidiabetic.

}, keywords = {Anti-inflammatory, Antidiabetic., Antioxidant, Cyperus Laevigatus, New Flavone}, doi = {10.5530/pj.2017.6.129}, url = {http://fulltxt.org/article/182}, author = {Abdelsamed Ibrahim Elshamy and Mohamed El-Shazly and Yomna Mahmoud Yassine and Mona Anwar El-Bana and Abdel- Razik Farrag and Mahmoud Ibrahim Nassar and Abdel Nasser Singab and Masaaki Noji and Akemi Umeyama} } @article {223, title = {The Serum Protein Fractions in Streptozotocin (STZ) Administrated Rat Models}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {December 2016}, pages = {35-38}, type = {Original Article}, chapter = {35}, abstract = {

Background: Experimental diabetes can be induced using chemical agents such as streptozotocin. Objective: This study aimed to investigate the effect of streptozotocin (STZ) which is most important agent to produce experimental diabetic model at two different doses on serum protein fractions in rat models. Materials and Methods: Twenty-four male rats that weighed an average of 250 g and were 3\–4 months old were used as the experimental models. They were sorted into three groups composed of eight rats each of STZ 55 mg/kg, STZ 65 mg/kg and control. Diabetes was induced by administering STZ 55 mg/kg and 65 mg/kg intraperitoneally. The serum protein fractions were analyzed by cellulose acetate electrophoresis. Results: No significant difference was observed between the groups for all fractions except alpha-2 and beta globulins. The alpha-2 and beta globulin levels were significantly higher in the 55 mg/kg group than in the 65 mg/kg STZ and control groups (p\<0.05). Conclusion: This increase may be due to the involvement of different proteins in the alpha-2 and beta globulin protein fractions.

}, keywords = {electrophoresis, experimental diabetes, Rat, serum proteins, STZ}, doi = {10.5530/pj.2017.1.7}, author = {Cennet Ragbetli and Semiha Dede and Feride Koc and Veysel Yuksek and Murat Cetin Ragbetli} } @article {211, title = {Antioxidant and Hypoglycemic Activities of Clausena anisata (Willd.) Hook F. Ex Benth. Root Mediated Synthesized Silver Nanoparticles}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {September 2016}, pages = {579-586}, type = {Original Article}, chapter = {579}, abstract = {

The present study was carried out to examine the hypoglycemic effect of Silver Nanoparticles (SNPs) using ethanolic root extract of Clausena anisata (Willd.) Hook. f. ex Benth. A cost effective and eco friendly technique for green synthesis of SNPs from 1mM AgNO3 solution through the root extract was carried out. The biosynthesized SNPs were characterized using UV spectrophotometry, Field Emission Scanning Electron Microscopy (FESEM), X-ray Diffraction analysis (XRD), Energy Dispersive Spectroscopy (EDS) and Fourier transform infra-red (FTIR) spectrometry. DPPH assay was done to determine the antioxidant activity and for in vitro hypoglycemic activity glucose uptake by yeast cells, alpha amylase inhibition assay, adsorption capacity and glucose diffusion assay was performed. The SNPs of ethanolic root extract were found to be spherical in shape and up to 32.75 nm average in size. They showed alpha amylase inhibitory activity of 83.60\% at 500 g/ml. The glucose uptake by yeast cells was found to increase with an increase in concentration. The maximum glucose uptake was found to be 69.51\% at 10mM concentration. The molar concentration of glucose was directly proportional to the glucose binding capacity of extracts.The rate of glucose diffusion across the membrane was found to increase from 30 to 180 minutes. The DPPH scavenging activity was found to be potent (74.07\%) at 500 g/ml. The hypoglycemic effect exhibited by the SNPs was revealed by simple in vitro model of yeast cells, mediated by glucose adsorption, increasing glucose diffusion and glucose transport across the cell membrane.

}, keywords = {antioxidant activity, C. anisata, Diabetes, Glucose and Silver nitrate, Silvernanoparticles}, doi = {10.5530/pj.2016.6.10}, author = {Arsia Tarnam Yakoob and Nargis Begum Tajuddin and Muhammad Ilyas Mohammed Hussain and Shilu Mathew and Archunan Govindaraju and Ishtiaq Qadri} } @article {129, title = {Assessment of Total Phenolic, Flavonoid, Tannin Content and Phytochemical Screening of Leaf and Flower Extracts from Peltophorum pterocarpum (DC.) Backer ex K.Heyne: a comparative study}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {December 2015}, pages = {140-143}, type = {Original Article}, chapter = {140}, abstract = {

Introduction: Total phenolic, flavonoid and tannin content of leaf and flower extract of Peltophorum pterocarpum (DC.) Backer ex K.Heyne was compared. Objective: To explore total phenolic, flavonoid and tannin content of both leaf and flower extracts of Peltophorum pterocarpum (DC) K Heyne. Method: Initially, collected fresh leaves and flower samples were shade dried and extracted with various solvents such as aqueous methanol (1:1), ethyl acetate, ethanol and aqueous. Qualitative analysis was performed for various phytochemical. Then the total phenolic content, total flavonoid content and total tannin content was estimated. Results: In preliminary phyto-chemical examination of various solvent extracts of both leaf and flowers of P. pterocarpum revealed that the presence of various phytochemicals such as phlobatannins, terpenoids, alkaloids, saponins, tannin, reducing sugars, phenols and steroids. In phtyochemical evaluation, when compare with all other solvents, Ethanolic extracts shows maximum extractive value. In case of ethyl acetate, it shows very low extractive value in all three phyto-chemicals. In phytochemical evaluation studies, total phenolic content of leaves shows highest in ethanolic extract (33.17 \± 4.72 mg/g) and lowest in ethyl acetate extract from flower (4.71 \± 0.07 mg/g), Similarly, flavonoid content of leaves shows highest in ethanolic extract (1.43 \± 0.01 mg/g) and lowest in aqueous extract of flower (0.23 \± 0.09 mg/g) but in case of tannin content, flower extracts shows higher tannin content in ethanolic extract (844.59 \± 10.38 mg/g) whereas lowest tannin content in leaf ethyl acetate extract (9.54 \± 6.98 mg/g). Conclusion: This is first report of comparative studies on total phenolic, flavonoid and tannin content of various solvent extracts both leaves and flowers from Peltophorum pterocarpum (DC) K Heyne.

}, keywords = {Flavonoid, Peltophorum pterocarpum, Phenolic content, Phytochemicals, Solvent extraction., Tannin}, doi = {10.5530/pj.2016.2.7}, author = {Peraman Muthukumaran and Nachimuthu Saraswathy and Vijayasekar Aswitha and Ramesh Balan and Venkatesh Babu Gokhul and Palanikumar Indumathi and Sivasubramani Yuvapriya} } @article {210, title = {Gc-Ms Analysis of Ethanolic Stem Extract of Clausena anisata (Willd.) Hook F Ex Benth}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {September 2016}, pages = {576-578}, type = {Original Article}, chapter = {576}, abstract = {

Objective: In the present study, the bioactive components present in the ethanol stem extract of Clausena anisata was analyzed by using Gas Chromatography Mass Spectrometry analysis technique (GC-MS). Clausena anisata, a medicinal plant belonging to the family Rutaceae, is represented by 20 species available in India and used traditionally for the treatment of several ailments but there is a requirement to identify its phytoconstituents, its target, mode of action and treatment using plant products either alone or in combination with synthetic drugs. Methods: Clausena anisata stem was procured from Manamettupatti, a village of Pudukottai District, Tamil Nadu. The shade dried stem was powdered and extracted using ethanol by maceration method. One microlitre of the extract was subjected to GC-MS analysis to detect the presence of bioactive compounds present in the stem of C. anisata. Results:The results showed that the ethanol stem extract of C. anisata contained nine bioactive compounds, of which the major one is n-hexadecanoic acid (78.54\%), followed by 8-octadecenoic acid, methyl ester, [E]- (6.638\%). The total number of compounds obtained was compared with National Institutes of Standard and Technology (NIST) library that contains more than 62,000 known compounds based on retention time and molecular mass. Conclusion: In this study, nearly nine compounds have been identified from the ethanolic stem extract of C. anisata using GC-MS analysis which was mainly composed of fatty acids and sterols. The GC-MS analysis is used to understand the nature of active principles present in this plant revealed that the plant can be used as a potential source of new useful drugs.

}, keywords = {C. anisata, Ethanol, GC-MS analysis, maceration and phytoconstituents}, doi = {10.5530/pj.2016.6.9}, author = {Arsia Tarnam Yakoob and Nargis Begum Tajuddin and Shilu Mathew and Muhammad Ilyas Mohammed Hussain and Ishtiaq Qadri} } @article {209, title = {Green synthesis, Antioxidant Potential and Hypoglycemic Effect of Silver Nanoparticles using Ethanolic Leaf Extract of Clausena anisata (Willd.) Hook. F. Ex Benth. of Rutaceae}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {September 2016}, pages = {565-575}, type = {Original Article}, chapter = {565}, abstract = {

The current study was conducted to examine the hypoglycemic effect of Silver Nano particles (SNPs) using ethanolic leaf extract of Clausena anisata (Willd.) Hook f. ex Benth. A cost effective and eco-friendly technique for the green synthesis of SNPs from 1mM AgNO3 solution through the leaf extract was carried out. The biosynthesized SNPs were characterized using UV spectro photometry, Field Emission Scanning Electron Microscopy (FESEM), X-ray Diffraction analysis (XRD), Energy Dispersive Spectroscopy (EDS) and Fourier transform infra-red (FTIR) spectrometry. DPPH assay was done to determine the antioxidant activity and for in vitro hypoglycemic activity glucose uptake by yeast cells, alpha-amylase inhibition assay, adsorption capacity and glucose diffusion assay was carried out. The SNPs of ethanol leaf extract were found to be spherical in shape and up to 60.67 nm average in size. They showed alpha-amylase inhibitory activity of 80.32\% at 500 g/ml and IC50 100 g/ml. The glucose uptake by yeast cells was found to increase with an increase in concentration. The maximum glucose uptake was found to be 68.29\% at 10mM concentration. The molar concentration of glucose was directly proportional to the glucose binding capacity of extracts. The rate of glucose diffusion across the membrane was found to increase from 30 to 180 minutes. The DPPH scavenging activity was found to be potent (71.60\%) at 500 g/ml. The hypoglycemic effect exhibited by the SNPs was revealed by simple in vitro model of yeast cells, mediated by glucose absorption, increasing glucose diffusion and glucose transport across the cell membrane.

}, keywords = {Nil}, doi = {10.5530/pj.2016.6.8}, author = {Arsia Tarnam Y and Nargis Begum T and Muhammad Ilyas MH and Shilu Mathew and Archunan Govindaraju and Ishtiaq Qadri} } @article {105, title = {Induction of hairy roots and plant regeneration from the medicinal plant Pogostemon Cablin}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {09/2015}, pages = {50-55}, type = {Original Article}, chapter = {50}, abstract = {

An efficient transformation system for the medicinal and aromatic plant, Pogostemon cablin Benth was developed by using Agrobacterium rhizogenes ATCC15834 and C58C1. Hairy roots formed directly from the cut edges of leaf explants after infection for 2 days. The highest frequency of leaf explant transformation by A. rhizogenes ATCC15834 and C58C1 were 83.3\% and 80.5\% after pre culture about 2 days and infection by the bacterium containing 15 mg l-1 acetosyringone about 25 min. The PCR amplification showed that rolB genes of Ri plasmid of A. rhizogenes were integrated and expressed into the genome of transformed hairy roots. The optimum medium for callus induction of hairy roots consisted of 2.0 mg l-1 benzyladenine (BA) and 0.1 mg l-1 a-naphthaleneacetic acid (NAA); while optimum medium for adventitious shoot regeneration from these cultures consisted of 0.1 mg l-1 BA and 0.1 mg l-1 NAA. Adventitious shoots could be rooted on 1/2MS. PCR analysis confirmed that rol genes of TL-DNA of Ri plasmid was integrated with at least three copies into the genome of hairy roots-regenerated P. cablin plants. The results presented provide a possibility for breeding of a new cultivar of P. cablin.

}, keywords = {Agrobacterium rhizogenes, ATCC15834., C58C1, Plant regeneration, Pogostemon cablin.}, doi = {10.5530/pj.2016.1.11}, author = {Han-jing Yan and Meng-ling He and Wei-Jian Huang and Dong-mei Li and Xiao-fang Yu} } @article {159, title = {Isolation of flavonoid from Abies webbiana leaves and its activity}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {June/2016}, pages = {341-345}, type = {Original Article}, chapter = {341}, abstract = {

Background: Abies webbiana commonly known as Talispatra in Bengali and Hindi, Talispatram in Sanskrit and Indian Silver Fir in English. This is a large, tall, evergreen tree occurring in the Himalayan region from Kashmir to Assam in India. It comes under the Family: Pinaceae. The present study was designed for isolation of flavonoid from ethyl acetate extract of A. webbiana leaves and assessed their toxic effect on liver and kidney. Materials and Methods: The isolation of flavonoid using different chromatographic methods (thin layer and column chromatography). The isolated flavonoid was identified; Structures and chemical bonds were analyzed by using MP, FTIR, 1-H NMR and MS spectral analysis. Effect of flavonoid on liver and kidney was assessed by inducing (0.1 ml/kg) CCl4 (i.p.) and (6 mg/kg) Cisplatin (i.p.) respectively measured by biochemical marker of liver and kidney. Results and Discussion: It was identified that isolated compound was as 4\’-hydroxy quercetin on the basis of FTIR, 1-H NMR and MS spectral analysis. Isolated flavonoid reduced the increased biochemical marker (BM) of liver and kidney. The BM was increased by inducing CCl4 and Cisplatin respectively. Conclusion: Isolated compound was 4\’-methoxy quercetin and significantly protect the liver and kidney.

}, keywords = {1-H NMR, Abies webbiana, CCl4., Cisplatin, Quercetin}, doi = {10.5530/pj.2016.4.6}, author = {Dinesh Kumar Yadav and Mohammed Ali and Ashoke Kumar Ghosh and Babita Kumar} } @article {186, title = {Macro-Microscopic evaluation, Physicochemical analysis and HPTLC Finger printing of Curculigo orchioides Gaertn. Rhizome}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {Oct 2016}, pages = {430-434}, type = {Original Article}, chapter = {430}, abstract = {

Introduction: Curculigo orchioides Gaertn. Family Hypoxydaceae (Amaryllidaceae) is a perennial herb with finger like rhizome. Its rhizomes have been significantly used in treatment of various ailments including cancer. Methods: Macro-microscopic analyses, physico-chemical studies and HPTLC finger printing of rhizomes of C. orchioides were performed according to pharmacopoeial procedures. Results: Microscopic analysis has shown rows of rectangular and conical cells in cork, thin walled cortex, parenchymatous cells, starch grains, crystal of calcium oxalate, mucilage cell and spiral xylem vessel in the rhizomes of C. orchioides. Physicochemical studies revealed loss on drying (10.469\%), total ash (8.463\%), acid insoluble ash (1.10\%), water-soluble ash (2.163\%), alcohol soluble extractive value (3.036\%), and water-soluble extractive value (22.666\%) of the raw drug. Ethanol extract of the plant were fingerprinted in petroleum ether and ethyl acetate (7.0:3.0) solvent system and scanned densitometrically after dipping in anisaldehyde-sulphuric acid reagent followed by heating at 105\°C. Conclusion: These specific identities will be useful in identification and authentication of the raw drug in dried form.

}, keywords = {Curculigo orchioides, HPTLC fingerprinting, Pharmacognostic, Quality control., Standaridisation}, doi = {10.5530/pj.2016.5.3}, author = {Deepa Yadav and Mohd Salim Reshi and Sadhana Shrivastava and Nalini Srivastava and Sunil Kumar Koppala Narayana and Sangeeta Shukla} } @article {141, title = {Pharmacognostic and Preliminary Phytochemical Investigation of Leaves of Aralia Racemosa L.}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {January 2016}, pages = {250-254}, type = {Original Article}, chapter = {250}, abstract = {

Objective: Ethnomedicinally, the entire plant and its parts are generally utilized by local people for the treatment of different aliment conditions without standardization. The standardization of crude drug is a crucial part of establishing its correct identity. Prior to any crude drug can be included in an herbal pharmacopeia, pharmacognostic and physicochemical param\­eters and standards to be established. Aralia racemosa L. perennial herb belongs to family Araliaceae. It is commonly known as American Spike\­nard. It is traditionally used in the treatment of Rheumatism, Whooping cough, skin diseases, pleurisy, diaphoretic, diuretic, pulmonary diseases, asthma, rheumatism, diarrhea, stimulant, expectorant, syphilis, Inflamma\­tion and Hay fever. In the view of lack of pharmacognostic study of leaf of Aralia racemosa L. Methods: The macroscopical, microscopical and physicochemical parameters were assessed according to WHO Quality Control Methods for herbal materials. The leaves of Aralia racemosa. L was subjected for successive solvent extraction and preliminary phytochemical screening was carried out, along with florescence analysis of leaf Pow\­der with different reagents were evaluated. Results: Macroscopy of the leaves showed oval to rounded shape with tooted margin, cordate base and pointed tip. Microscopic studies revealed the presence of anisocytic stomata, bicolateral vascular bundles, lignified fibers, spiral vessels and rosette shaped calcium oxalate crystals. Physicochemical parameters such as moisture content, extractive values, ash content and fluorescent behav\­ior of leaf powder were also determined. Preliminary Phytochemical analy\­sis revealed the presence of various phytochemical constituents viz., glyco\­sides, tannins, flavonoids, saponins and steroids. Conclusion: The results of current study could be served as a diagnostic tool for the standardization of this medicinal plant and will helpful in characterization of the crude drug.\ 

}, keywords = {Anisocytic stomata, Aralia racemosa, Bicolateral vascular bundles, Lignified fibers., Pharmacognostic, Rosette shaped calcium oxalate crystals}, doi = {10.5530/pj.2016.3.13}, author = {D S N B K Prasanth and Atla Srinivasa Rao and Rajendra Prasad Yejella} } @article {57, title = {Dynamic Comparison of Free Radical Scavenging Abilities of Hypericum Perforatum L., Herba Verbenae Officinalis, and Valeriana Officinalis L. Extracts}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {198-204}, type = {Original Article}, chapter = {198}, abstract = {

Objectives: The purpose of this research was to compare the dynamic antioxidant activities and the free radical scavenging abilities of three botanical supplements, Hypericum perforatum L. (HPL), Herba Verbena Officinalis (HVO), and Valeriana officinalis L. (VO), which have been reported to effectively treat menopause symptoms. Methods: The antioxidant activities of the three supplements were determined by the ferric reducing ability of plasma (FRAP) assay. In addition, their free radical scavenging abilities were studied by ftheir interactions with the stable radicals of 2, 2\’-azino-bis-(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) and 2,2-diphenyl-1-picrylhydrazyl (DPPH). Results: The results indicated that the HPL ethanolic extract exhibited greater antioxidant activity (1.2688 \± 0.01 mmol Trolox/g) than the HVO ethanolic extract (1.1686\± 0.043 mmol Trolox/g) and the VO ethanolic extract (0.2579 \± 0.0031 mmol Trolox/g) as compared to Nilestriol (0.0026\±0.0012), a positive control agent in the experiment. Moreover, the HPL extract showed remarkable free radical scavenging activity against ABTS\•+, and the HVO extract was the most potent against DPPH\•. Conclusion: These activities may be attributed to the total flavonoid or phenolic acid contents of among these extracts.

}, keywords = {ABTS{\textbullet}+, DPPH{\textbullet}, Herba Verbena Officinalis, Hypericum perforatum L., Menopause Oxidative Stress, Valeriana officinalis L.}, doi = {10.5530/pj.2015.3.9}, author = {Yi-ming Li and Yan-Ru Liu and Bing-Kun Xiao and Jian-Yun Yang and Rong-Qing Huang} } @article {1476, title = {Dynamic Comparison of Free Radical Scavenging Abilities of Hypericum Perforatum L., Herba Verbenae Officinalis, and Valeriana Officinalis L. Extracts}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {09th Mar, 2015}, pages = {198-204}, type = {Original Article}, chapter = {198}, abstract = {

Objectives: The purpose of this research was to compare the dynamic antioxidant activities and the free radical scavenging abilities of three botanical supplements, Hypericum perforatum L. (HPL), Herba Verbena Officinalis (HVO), and Valeriana officinalis L. (VO), which have been reported to effectively treat menopause symptoms. Methods: The antioxidant activities of the three supplements were determined by the ferric reducing ability of plasma (FRAP) assay. In addition, their free radical scavenging abilities were studied by ftheir interactions with the stable radicals of 2, 2\’-azino-bis-(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) and 2,2-diphenyl-1-picrylhydrazyl (DPPH). Results: The results indicated that the HPL ethanolic extract exhibited greater antioxidant activity (1.2688 \± 0.01 mmol Trolox/g) than the HVO ethanolic extract (1.1686\± 0.043 mmol Trolox/g) and the VO ethanolic extract (0.2579 \± 0.0031 mmol Trolox/g) as compared to Nilestriol (0.0026\±0.0012), a positive control agent in the experiment. Moreover, the HPL extract showed remarkable free radical scavenging activity against ABTS\•+, and the HVO extract was the most potent against DPPH\•. Conclusion: These activities may be attributed to the total flavonoid or phenolic acid contents of among these extracts.

Key words: ABTS\•+, DPPH\•, Hypericum perforatum L.,Herba Verbena Officinalis, Menopause Oxidative Stress, Valeriana officinalis L.

}, keywords = {ABTS{\textbullet}+, DPPH{\textbullet}, Herba Verbena Officinalis, Hypericum perforatum L., Menopause Oxidative Stress, Valeriana officinalis L.}, author = {Yi-ming Li and Yan-Ru Liu and Bing-Kun Xiao and Jian-Yun Yang and Rong-Qing Huang} } @article {78, title = {Hepatoprotective effect of Livplus-A polyherbal formulation}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {311-316}, type = {Original Article}, chapter = {311}, abstract = {

Objective: The aim of the present study was to investigate the hepatoprotective effect of Livplus (a polyherbal formulation) against CCl4-induced hepatotoxicity in rats. Methods: Hepatotoxicity was induced in rats by i.p. injection of CCl4 once three days for 14 days. Livplus or Silymarin was administered along with CCl4 and the biochemical parameters like aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkalinephosphatase (ALP), total bilirubin (TB), direct bilirubin, total protein (TP), gamma-glutamyl transferase (GGT), total cholesterol (TC) and triglycerides (TG) were estimated. Furthermore, biomarkers of oxidative stress such as MDA levels, Glutathione contents, SOD and catalase activity in liver tissue were estimated. Results: Treatment with Livplus significantly reduced the elevated levels of ALT, AST, ALP, bilirubin (direct and total), GGT, TC, TG and increased levels of TP compared to CCl4 control rats. The treatment with Livplus also showed a significant increase in glutathione contents, SOD and catalase activity and a decrease in MDA levels compared to CCl4 control rats. Conclusion: The finding of present study indicates that Livplus showed a potential hepatoprotective activity. These results support the traditional use of Livplus in the treatment of liver disorders.

}, keywords = {CCl4, GGT, Hepatic enzymes., Hepatotoxicity, Livplus}, doi = {10.5530/pj.2015.5.11}, author = {Rajesh Maheshwari and Bhagyashree Pandya and Ramachandran Balaraman and Avinash Kumar Seth and Yogesh Chand Yadav and Vasa Siva Sankar} } @article {1483, title = {Anti-inflammatory and hepatoprotective activities of methanolic extract of Anthemis scrobicularis herbs}, journal = {Pharmacognosy journal}, volume = {6}, year = {2014}, month = {8th April 2014}, pages = {55-61}, type = {Original Article}, abstract = {

The anti-inflammatory and hepatoprotective activitiesof the methanolic extract of Anthemis scrobicularis(ANS) herbs were evaluated in rats against carrageenan induced inflammation and carbon tetrachloride (CCl4)induced hepatic injury. To evaluate the anti-inflammatory effects of ANS, twenty male rats were divided into four equal groups. Injection of 100 \μl carrageenan in normal saline into the subplantar region of the hind paw of rats clearly induced paw edema. The volume of paw edema was attenuated following oral administration of ANS. For hepatoprotective effects, twenty five rats were equally divided into five groups.The hepatotoxicity, induced by a single dose of CCl4, produced significant (p\<0.001) increase of the levels of serumtransaminase, phosphatase, bilirubin and a decrease in proteins were also noticed. The oxidative stress marker such as malondialdehyde (MDA)was increased and nonprotein sulfhydryl (NP-SH) was decreased in the hepatotoxic tissues. Pre-medication of CCl4-intoxicated rats with ANS at the doses 250 and 500 mg/kg reversed the abnormal liver diagnostic stricture. The results showed that ANS is toxicologically safe when orally administered and possess highly significant anti-inflammatory and hepatoprotective activities and the potentials usefulness of Anthemis scrobicularis in hepatic and inflammatory disease.

Key words: Anthemis scrobicularis, Anti-inflammatory, Hepatoprotective, Carbon tetrachloride, Histopathology.

}, keywords = {Anthemis scrobicularis, Anti-inflammatory, Carbon tetrachloride, Hepatoprotective, Histopathology}, author = {Hasan S. Yusufoglu and Aftab Alam and Mohamad Ayman A. Salkini and Ahmed M. Zaghloul} }