@article {1386, title = {Anti-Cancer Activity of Cayratia Auriculata Ethanolic Extracts Against Cancer Cell Line A549 An In Vitro Analysis}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {March 2021}, pages = {495-499}, type = {Research Article}, chapter = {495}, abstract = {

Background: The purpose of this study was to evaluate the anticancer activity of ethanolic cayratia auriculata extracts using the A549 cell line MTT assay. Materials and Methods: Using Soxhlet apparatus, ethanolic extracts from cayratia auriculata were prepared. The cancer cells were exposed to 12.5, 25, 50 , 100 , 150, 200 μg / mL and incubated for 24 h at different concentrations. Compared with control, C. auriculata exhibited a cytotoxic effect. Results: At 150 and 200μg / ml concentrations, with 61 percent and 73.7 percent respectively, the highest cytotoxicity was identified. The findings show that cytotoxicity is directly proportionate to the concentration of the extract. IC50 of the ethanolic extract value of C. auriculata was found to be 102.9μg / ml against the A549 cell line. Conclusion: In the present analysis, C.auriculata ethanolic extract was shown to be a strong suppressant for cell division and proliferation. As for anti-tumor medicine, it can be a new source and can be effectively used as an immunological anti-malignant compound.

}, keywords = {Activity against cancer, Cell line cancer, Ethanol Extract, MTT Assay}, doi = {10.5530/pj.2021.13.62}, author = {S Lalitha and D Anusha and Yogeshkumar Murkunde and Viji Devanand and K Maheshkumar} } @article {1370, title = {Cytotoxicity Study of Ethanol Extract of Bintangor Leaf (Calophyllum soulattri Burm.f) on T47D Breast Cancer Cell Line (Cytotoxicity Study with MTT Assay Method)}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {March 2021}, pages = {362-367}, type = {Original Article}, chapter = {362}, abstract = {

Introduction: The public has used Bintangor leaf (Calophyllum soulattri Burm.f) for various medical treatments, including treated inflamed eyes and gout. Aim: This research aimed to determine the cytotoxic effect of ethanol extract and fraction of Calophyllum soulattri Burm. f leaf toward T47D breast cancer cell. Methods: The test used T47D breast cancer cells, the 3-4,5-dimethylthiazol-2yl -2,5-diphenyltetrazolium bromide (MTT) test method, and ELISA Reader to determine the absorbance. This method{\textquoteright}s principle was the presence of tetrazolium salts by the reductase system in the mitochondria of living cells formed purple formazan crystals. The used parameter was the value of IC50. Results: The result showed that ethanol extract, n-hexane fraction, ethyl acetate fraction, and butanol fraction did not have a cytotoxic effect on T47D breast cancer cell. The values of IC50 respectively are 585.31 μg/ml; 409.33 μg/ ml; 534.08 μg/ml; and 563.22 μg/ml. Conclusion: Ethanol extract and Calophyllum soulattri Burm.f leaf fraction did not have a cytotoxic effect on T47D breast cancer cells.

}, keywords = {Bintangor Leaf, Breast Cancer Line, Calophyllum soulattri Burm.f, Cytotoxicity, MTT Assay, T47D}, doi = {10.5530/pj.2021.13.46}, author = {Elidahanum Husni and Fatma Sri Wahyuni and Hanifa Nurul Fitri and Elsa Badriyya} } @article {1166, title = {Assessment of the Impact of Wild Stinkhorn Mushroom Extracts on Different Cancer Cell Proliferation and Study of Primary Metabolites}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {699-708}, type = {Original Article}, chapter = {699}, abstract = {

Objective: Present study aims to evaluate the efficacy of methanolic and ethyl acetate extracts of wild mushroom Phallus sp. on cell proliferation of both normal and cancer cells. This study also looked at anti-oxidant potentiality of methanolic extract and also unravels the phytochemical profiling of both extracts. Methods: Anti-proliferative activity was assessed by MTT assay on different human cancer cell lines such as MCF-7, MOLT-4, REH and Peripheral Blood Mononuclear Cells or PBMC isolated from a healthy donor. Gas Chromatography-Mass Spectrometry (GC-MS) analysis was used for comparative assessment of phytochemical constituents of both extracts. The anti-oxidant profile of methanolic extract was also evaluated by DPPH and ABTS{\textbullet}+ assays. Results: Results indicated that the both methanolic and ethyl acetate extracts of Phallus sp. showed appreciable anti-proliferative activity against breast cancer cell line MCF-7 with IC50 of 8.544{\textpm}2.812 μg/mL and 35.279{\textpm}2.863 μg/mL respectively. Both of the extracts also showed its moderate impact on human B cell precursor leukemia cell line (REH) with IC50 of 25.987{\textpm}2.696 μg/mL for methanol and 51.484{\textpm}1.480 μg/mL for ethyl acetate extract respectively. No effect was observed in MOLT-4 cell line. Methanolic extract was selected as better anti cancer extract over ethyl acetate extract. No significant anti-proliferative activity was observed in normal PBMC by both extracts. GC-MS analysis indicated that 43 and 114 compounds were identified from methanolic and ethyl acetate extracts respectively. Among them nine compounds shared its existence in both of the extracts. Different derivatives of ergosterol and several fatty acid esters ware identified as major components from both of the extracts. Methanolic extracts of the Phallus sp. showed its effectiveness on both of DPPH and ABTS{\textbullet}+ free radical, and result indicated that it contain more flavonoid content than phenol. Conclusion: The methanolic extract of Phallus sp. show very specific anti-proliferative effect on MCF-7 with moderate anti-oxidant activity and holds a great promise for isolation of bio molecules for treating Breast Cancer. Several derivatives of ergosterol identified as probable anti-cancer compound.

}, keywords = {ABTS{\textbullet}+, GC-MS, MCF-7, MTT Assay, Phallus}, doi = {10.5530/pj.2020.12.102}, author = {Ribhu Ray and Amrita Pal and Santanu Paul} } @article {1056, title = {Evaluation of Anti-proliferative Potential and Antioxidant Activity of a Wild Edible Mushroom Macrocybe crassa (Sacc.) Pegler and Lodge}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {November 2019}, pages = {1504-1510}, type = {Original Article}, chapter = {1504}, abstract = {

Objective: This study aims to quantify the anti-oxidant activity of the methanolic extract of Macrocybe crassa and its anti-proliferative activity on normal and cancer cells. Methods: The anti-oxidant potential of the extract was determined by several in vitro assay system like DPPH radical scavenging activity, superoxide anion scavenging activity, percentage inhibition of lipid peroxidation and nitric oxide (NO) scavenging activity. Anti-proliferative activity was tested by MTT assay on breast cancer cell line MCF7, Human acute T lymphoblastic leukaemic cell MOLT-4 and Peripheral Blood Mononuclear Cells or PBMC isolated from a healthy donor to check its cytotoxic effect on normal cells. Results: Results indicated that the methanolic extract of Macrocybe crassa shows appreciable anti-proliferative activity against breast cancer cell line MCF7 and negligible effect on MOLT4 cells. In contrast no significant anti-proliferative effect has been observed in normal PMMCs. Moderate anti-oxidant activity was recorded in methanolic extract. Conclusion: Methanolic extract of of Macrocybe crassa with moderate anti-oxidant activity and specific anti-proliferative effect on MCF7 holds a great promise can be used for isolation of bio molecules for treating Breast Cancer.

}, keywords = {Antioxidant, Macrocybe crassa, MCF7, MOLT-4, MTT Assay}, doi = {10.5530/pj.2019.11.231}, author = {Amrita Pal and Anirban Chouni and Arpan Das and Ribhu Ray and Santanu Paul} } @article {904, title = {In vitro Antidiabetic Activity of Methanolic Leaf Extract of Indianthus virgatus (Roxb.) Suksathan and Borchs by Glucose Uptake Method}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {674-677}, type = {Original Article}, chapter = {674}, abstract = {

Medicinal plants play a key role to cure many diseases from time immemorial. The usage of medicinal plants in traditional medicinal system is the vital process of India. Diabetes Mellitus is a systemic metabolic disease characterized by hyperglycemia, abnormal elevated levels of lipid and fat in blood and hypoinsulinaemia. The current epidemic of diabetes indicates the need of proper and effective medications that are limited in their potency to have many side effects. Thus, introduction of alternative and complementary medicine is now in picture. Objective: The main objective of this work is to evaluate the in vitro anti diabetic activity of methanolic extracts of Indianthus virgatus (Roxb.) Suksathan and Borchs in skeletal muscle cell line. Methods: The in vitro cytotoxicity was performed for leaf extract (Methanol) on L-6 (Rat skeletal muscle) cell line to find toxic concentration of the leaf extract by MTT assay. Glucose uptake activity of test substance was determined in differentiated L-6 cells. Results: In Glucose uptake assay, Methanol Extract exhibited moderate toxicity to skeletal muscle cell line and glucose uptake assay it shows dose dependent glucose uptake. Glucose uptake rate increased with the increasing concentration of the leaf extract. Conclusion: The results of the current study clearly demonstrated the antidiabetic potency of methanolic leaf extract obtained from Indianthus virgatus (Roxb.) Suksathan and Borchs. under in vitro model.

}, keywords = {Antidiabetic activity, In vitro cytotoxicity, Indianthus virgatus (Roxb.) Suksathan and Borchs, L-6 cell line, Methanolic leaf extract, MTT Assay, Skeletal muscle Cell Lines, Therapeutic agents}, doi = {10.5530/pj.2019.11.106}, author = {Sangeetha DN and S. Rajamani} } @article {915, title = {Investigation of Secondary Metabolites and Cytotoxicity of Jacquemontia pentantha (Jacq.)}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {718-723}, type = {Original Article}, chapter = {718}, abstract = {

Introduction: The aim of this study is to isolate and identify sterols and terpenes from the chloroform/methanol extract (3:1) of aerial parts of Jacquemontia pentantha (Jacq.) and evaluation of cytotoxic activity of crude extract and phytol for the first time from this plant. Methods: Different chromatographic techniques for the aerial parts of Jacquemontia pentantha extract were used resulting in isolation of eight compounds. Their structures were elucidated by spectroscopic methods including 1HNMR, 13CNMR, EI/MS spectrometry and by comparing their data with those reported in the literature. The cytotoxicity was evaluated using MTT assay. The mode of action of the extract was predicted by using Enzyme-linked Immunosorbent Assay Kit for Tubulin beta (TUBb). Results: Eight compounds for the first time from this plant were identified as Palmitic acid (1), Phytol (major) (2), Stigmast-4-en- 3-one (3), mixture of α-amyrin (4) and β{\textendash}amyrin (5), 1,6,10,14,18,22-Tetracosahexaen-3- ol,2,6,10,15,19,23-hexamethyl (all-E) (6) and mixture of α{\textendash} amyrin acetate (7) and β-amyrin acetate (8). The extract showed potent cytotoxic activity on MCF-7 breast carcinoma cell line as well as HCT-116 colon carcinoma cell line at different concentrations (100-6.25 ug/ml) with IC50 (21.8 {\textpm} 0.9) and (40.9 {\textpm} 1.3) respectively. Phytol showed potent cytotoxic activity on MCF-7 cell line at different concentrations (100-12.5 ug/ml) with IC50 (60 {\textpm} 2.4), while it had no cytotoxic effect on HCT-116 cell line. The extract showed significant TUBb polymerization inhibition activity. Conclusion: The extract of aerial parts of Jacquemontia pentantha (Jacq.) and also phytol compound has cytotoxic activity due to the presence of phytochemicals such as sterols and terpenes.

}, keywords = {Cytotoxic activity, Enzyme-Linked Immunosorbent Assay, Jacquemontia pentantha, MTT Assay, Sterols, Terpenes}, doi = {10.5530/pj.2019.11.114}, author = {Dina M Eskander and Ezzel -Din A El-Khrisy and Mary H Grace and Marian Nabil and Mahmoud I Nassar and Marwa M Mounier} } @article {466, title = {Cytotoxic Activities of Fractions from Dioscorea bulbifera L. Chloroform and Methanol Extracts on T47D Breast Cancer Cells}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {December 2017}, pages = {33-38}, type = {Original Article}, chapter = {33}, abstract = {

Objective: To elucidate cytotoxic activity of fractions from chloroform and methanol extracts of D. bulbifera organs on T47D breast cancer cells. Method: The vegetative organs of D. bulbifera were extracted gradually using chloroform and methanol. Cytotoxicity tested on T47D cells using MTT Assay. The most toxic extract was fractioned by vacuum liquid chromatography (VLC) followed by thin layer chromatography (TLC). The extract and fractions potential were tested on the Vero cells using the same method as cancer cells. The most toxic fraction was analyzed using TLC followed by the application of various spray reagents for the identification of active compound. Results: The chloroform extract of the D. bulbifera leaves was the highest cytotoxic on T47D cells (IC50 115.63\±86.01 \μg/mL). Moreover, the cytotoxicity test on the combined fractions of leaves chloroform extract showed that fraction 5 (F5) and fraction 6 (F6) were the most toxic fractions compared to those of other fractions. The IC50 of both fractions were 14.55\±8.62 and 7.12\±4.43 \μg/mL respectively. However, Its were very weak compared to those of cancer medicine (Doxorubicin) with the IC50 was 0.04\±0.02 \μg/mL. Potential fractions were not toxic against Vero cells with IS\>10. The active compounds in those fractions were alkaloid and terpenoid. Conclusion: Chloroform extract of the D. bulbifera leaves had the highest cytotoxic effect on T47D cells. Potential fractions were not toxic against Vero cells. The active compounds in those fractions were alkaloid and terpenoid.

}, keywords = {Cytotoxicity, D. bulbifera, MTT Assay, Secondary metabolites, T47D}, doi = {10.5530/pj.2018.1.7}, url = {http://fulltxt.org/article/362}, author = {Rinto Muhammad Nur and Laurentius Hartanto Nugroho} } @article {730, title = {Cytotoxic Activity of Ethanol Extract of Arbuscular Mycorrhizal Fungi Induced Ginger Rhizome on T47D Breast Cancer Cell Lines}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1133-1136}, type = {Original Article}, chapter = {1133}, abstract = {

Objective: A study of investigate the cytotoxicity activity of ethanolic extract of ginger (Zingiber officinale Rosc.) induced with arbuscular mycorrhizal fungi (AMF) against T47D cells line breast cancer have been conducted. Methods: Cytotoxicity were determined using the \“microtetrazolium (MTT) Assay\”, by measuring the activity of mitochondrial dehydrogenase in living cells that have ability to convert pale yellow of dissolved MTT to purple formazan product. The extract used at various concentration (0.1, 1.0, 10 and 100 \μg / mL. The level of cytotoxic actifity was determined by calculating the inhibitory concentration (IC50) value that was based on the precentage of cell death after 24 h treatment with the extract. The change of cell morphology were observed by using inverted microscope. Results: The statistic results proved that ethanol extract of AMF induced ginger rhizome could barriers T47D breast cancers significantly at concentrations of 10 \μg / mL and 100 ug / mL, with IC50 value was 12.5 \± 3.73 \μg / mL. centration of 0.1 \μg / mL, 1.0 \μg / mL, 10 \μg / mL and 100 mg / mL. Results of statistical analysis showed that the ethanol extract of ginger rhizome induced AMF at a concentration of 10 \μg / mL and 100 \μg / mL was able to inhibit the growth of breast cancer cells T47D significantly. Conclusion: The results showed the ethanol extract of AMF induced ginger rhizome was potential as herbal medicine for cancer-related ailments with IC50 value was 12.5 \± 3.73 \μg / mL.

}, keywords = {AMF, Breast cancer, Cytotoxicity, Ginger, MTT Assay, T47D}, doi = {xx10.5530/pj.2018.6.193}, author = {Netty Suharty and Fatma Sri Wahyuni and Dachriyanus} } @article {706, title = {In vitro Evaluation of Seaweed Gracilaria verrucosa for Cytotoxic Activity against Cervical HeLa Cells}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1007-1011}, type = {Original Article}, chapter = {1007}, abstract = {

Background: Seaweed macroalgae of Gracilaria verrucosa has been known to have a potent anticancer activity, however the cytotoxicity against cervical cancer has not been explored further. Objective: This study aims to utilize Indonesia\’s marine resource which is focused on seaweed macroalgae G. verrucosa as a future anti-cervical cancer agent. Materials and Method: Seaweed G. verrucosa originated from Labuan Aji beach, Nusa Tenggara Barat, Indonesia, extracted, macerated, and fractionated into four organic solvents of different polarity, consisting of hexane, ethyl acetate, chloroform and ethanol. Then, the macroalgae extracts are diluted into 8 different concentrations. Afterwards, in vitro anticancer activity evaluation of hexane, ethyl acetate, chloroform and ethanol extracts of G. verrucosa against cervical HeLa cells were conducted by MTT cell proliferation assay. Triplo mechanism is also applied in this study to increase the accuracy of the results. The anticancer activity is measured using IC50 value. Results: The four concentrated extracts G. verrucosa showed cytotoxicity against cervical HeLa cells. The greatest anticancer activity is depicted by hexane extract with an IC50 of 14.94 \μg/mL, followed by chloroform (IC50 15.74 \μg/mL), ethyl acetate (IC50 16.18 \μg/mL), and ethanol (IC50 19.43 \μg/mL). Conclusion: Our results clearly indicate that hexane, ethanol, chloroform, and ethyl acetate extracts of seaweed G. verrucosa can be further developed to be anti-cervical cancer agents, with hexane extract displaying the greatest cytotoxic effect.

}, keywords = {Cytotoxicity, Gracillaria verrucosa, HeLa cervical cancer cells, IC50 value, MTT Assay}, doi = {10.5530/pj.2018.5.171}, author = {Micheylla Kusumaning Dewi and Ade Arsianti and Cut Raisya Zahira Zagloel and Yully Astika Nugrahayning Aziza and Kartika Dwi Kurniasari and Baiq Kirana Dyahningrum Mandasari and Riathul Masita and Futihati Ruhama Zulfa and Norma Nur Azizah and Rista Putrianingsih} } @article {561, title = {Purified Anthocyanin, its Elicitation from Cell Cultures of Begonia malabarica and Begonia rex-cultorum {\textquoteleft}Baby Rainbow{\textquoteright}and it{\textquoteright}s In vitro Cytotoxicity Analysis by MTT Assay}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {March 2018}, pages = {553-558}, type = {Original Article}, chapter = {553}, abstract = {

Background: According to recent statistics, cancer accounts about marked percentage of total deaths in the world, although there are many therapeutic approaches. Unfortunately, the cytotoxicity properties of most chemotherapy drug are nonspecific and therefore do not distinguish between normal healthy cells and tumor cells, these events have led to inappropriate and toxic therapeutic agents with a wide range of side effects. However, several experimental and epidemiological studies have suggested that fruits and vegetables are associated with low risk of various types of cancer. Anthocyanins are natural pigments that provide intense purple to red color in plants. Anthocyanin possess the ability to inhibit oxidative stress and to induce apoptosis in malignant cells, thus may prevent carcinogenesis. Methods: Antiproliferative properties of purified anthocyanin extract from elicited cell suspension cultures of Begonia malabarica and Begonia rex-cultorum \‘Baby rainbow\’ was investigated in terms of MTT assay. Anthocyanin extracts were tested for their ability to inhibit the growth of HT29 (colon cancer cells), MG63 (Osteosarcoma), HeLa (Cervical cancer cells) and L929 (Mouse Fibroblast L929) cell lines. Results: Cell viability decreased in a dose dependent manner in all the considered cell lines treated with anthocyanin extracts. The extract of Begonia rex-cultorum \‘Baby rainbow\’ exhibited significant cytotoxic activity against all tumor cell lines than Begonia malabarica extract. Begonia malabarica and Begonia rex-cultorum \‘Baby rainbow\’ anthocyanin extract exhibited the highest cytotoxicity towards HT29 and HeLa cell lines respectively. But, MG63 resulted in comparatively higher percentage of viability of cell lines at the same concentrations. The anthocyanin extract produced significant morphological alterations on cell lines in culture. Meanwhile, the extracts showed poor cytotoxicity against the normal cell line. Conclusion: The morphological alteration of the treated cancer cells presented clear evidence of significant cytotoxicity of anthocyanin extracts of both Begonias in all the three cell lines. Thus, anthocyanin may act as chemopreventive agents for various cancer cell lines.

}, keywords = {Anthocyanin, Begonia, Cancer, Cell suspension., Cytotoxicity, MTT Assay}, doi = {10.5530/pj.2018.3.90}, url = {http://fulltxt.org/article/523}, author = {Aswathy Jayasree Madanakumar and Murugan Kumaraswamy} } @article {252, title = {Cytotoxic Effect of Caralluma fimbriata Against Human Colon Cancer Cells}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {February 2017}, pages = {204-207}, type = {Original Article}, chapter = {204}, abstract = {

Aim: The present study was designed to examine the cytotoxic effects of ethanolic leaf extract of Caralluma fimbriata in the COLO 320 cell line. Materials and Method: The anti-proliferative effects were evaluated using the MTT assay. The COLO 320 cells were treated with different concentrations of the leaf extract of Caralluma (100 \– 300 \μg/ml) for 24 h. The cell viability and IC50 was calculated from the cytotoxicity. The morphology of the Caralluma treated cells, control, and positive control were observed under reverse phase inverted microscope. Result: The C. fimbriata ethanolic leaf extract showed dose dependant increase in cytotoxicity in COLO 320 human colon cancer cells. The maximum cytotoxic effect was noticed with maximum dose used in this study i.e., 300 g with an IC50 value of 233.87 g. Conclusion: The present study shows that the ethanolic leaf extract of Caralluma fimbriata is capable of reducing cell proliferation by inducing cytotoxicity of COLO 320 cells.

}, keywords = {Caralluma fimbriata, COLO 320 cell line, Colonic cancer, Cytotoxicity, MTT Assay}, doi = {10.5530/pj.2017.2.34}, url = {http://phcogj.com/fulltext/301}, author = {Shenai Ashwini and Devaraj Ezhilarasan and Roy Anitha} } @article {423, title = {Cytotoxicity and Oral Acute Toxicity Studies of Litsea glutinosa C. B (ROB) Stem Bark Ethanol Extract}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {880-886}, type = {Original Article}, chapter = {880}, abstract = {

Background: Litsea glutinosa (Lauraceae) stem bark is widely used in folk medicine as a hepatoprotective, anti-diarrheal and anti-dysenteric drug but there is a lack of information about its toxicity. Objective: To evaluate cytotoxicity and acute toxicity of the stem bark ethanol extract (BEE). Materials and Methods: In vitro cytotoxicity of BEE was measured against breast adenocarcinoma, prostate, and colon carcinoma cell lines. In the acute toxicity tests, rats received oral doses of BEE as 1000, 2000, and 3000 mg/kg body weight. Mortality, signs of toxicity, body weight, food consumption, and gross findings were observed for 14 days. Blood samples were collected from anesthetized animals and used for hematological and biochemical parameters. Histopathological study was performed using liver and kidney samples. Results: The BEE does not show significant cytotoxic effect against the tested cell lines up to the range from 5 to 320 \μg/ml. In acute toxicity study, also lethality was not observed up to 3000 mg/kg b.w. No significant differences were noticed in body and organ weights and histopathology examinations between the control and treated groups. Conclusion: This study authenticates stem BEE may contain bioactive compounds of potential therapeutic significance which are relatively safe from toxic effects, and evidences the medicinal use of this plant in folk medicine.

}, keywords = {Acute toxicity, Breast adenocarcinoma cell line, Haematology., Litsea glutinosa, MTT Assay}, doi = {10.5530/pj.2017.6.138}, url = {http://fulltxt.org/article/191}, author = {Arunodaya Hosahalli Sumithregowda and Krishna Venkatarangaiah and Kumaraswamy Malleshappa Honnenahally and Vinaykumar Nagenahalli Manjunath} } @article {403, title = {Cytotoxicity Effect and Morphological Study of Different Duku(Lansium domesticum corr.) Extract towards Human Colorectal Adenocarcinoma Cells Line (HT-29)}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {757-761}, type = {Original Article}, chapter = {757}, abstract = {

Context: Lansium domesticum corr. is a member of the family Meliaceae, and known locally as duku and has been used traditionally in the prevention and treatment of various illness. Aim: To study the cytotoxic effect and morphological changes of human colorectal adenocarcinoma cells (HT-29) treated with different duku (Lansium domesticum corr.) extracts. Methods: The L.domesticum corr. fruit extracts were processed involving three different solvents; methanol, ethanol and ethyl acetate. HT-29 cell lines were treated with different concentrations of L. domesticum corr. (0-100 \μg/ml) extracts for a total of 24, 48 and 72 hours. Cytotoxicity of cells line was determined by using MTT assay as per IC50 values. Results: Methanol extract of L. domesticum corr. showed IC50 value at 6.79 \± 0.00 \μg/ml and 50.0 \± 0.00 \μg/ml respective, while ethyl acetate extract of L. domesticum corr. reached IC50 value at 86.00 \± 0.08 \μg/ml, and 96.0 \± 0.12 \μg/ml. There was no IC50 value of ethanol extract from L.domesticum corr. Only methanol extract showed toxicity towards HT-29 cells line. Conclusion: To the best of our knowledge, this is the first repeat the exploring the effect of duku (L. domesticum corr.) extract on HT-29 cells line.

}, keywords = {Anti-proliferative effect, colorectal cancer, IC50 value., MTT Assay, polarity extracts}, doi = {10.5530/pj.2017.6.119}, url = {http://fulltxt.org/article/172}, author = {Rohin Mohd Adzim Khalili and Jumli Mimie Noratiqah and Ridzwan Norhaslinda and Abd Hadi Norhayati and Baig Atif Amin and Arshad Roslan and A. Latif Ahmad Zubaidi} } @article {127, title = {In vitro Cytotoxicity Studies of Zn (Zinc) Nanoparticles Synthesized from Abutilon indicum L. against Human Cervical Cancer (HeLa) Cell Lines.}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {December 2015}, pages = {127-131}, type = {Original Article}, chapter = {127}, abstract = {

Background: The Zn nanoparticles synthesized from the plant sources are ecofriendly and are potent anticancer agents. Objective: The objective of the present work was to evaluate In vitro cytotoxic activity of Zn nanoparticles green synthezised from Abutilon indicum extract against HeLa cell lines (cervical cancer). Methods: The aqueous extract is prepared by cold extraction (maceration) using water as a solvent. Phytochemical analysis was done by using the standard procedures. Aqueous extract of A. indicum was used for synthesis of Zn nanoparticles. The nanoparticles were characterized by UV-Visible spectrometry and Scanning electron microscopy (SEM) techniques. In vitro cytotoxicity studies of Zn nanoparticles were done by MTT assay using HeLa cell lines. Results: The preliminary phytochemical results revealed that the aqueous extract of A. indicum contains broad spectrum of secondary metabolites like Tannins, Saponins, Glycosides, Flavonoids, Anthroquinones, Terpenoids and Steroids. The U.V spectrophotometeric analysis of Zn nanoparticles displayed maximum absorption at 270 nm and scanning electron microscopic studies showed that the nanoparticles size ranges from 50-500 nm. The MTT assay results revealed that the of Zn nanoparticles exhibits potent cytotoxicity against HeLa cell lines with IC50 value of 45.82 \μg/ml. Conclusion: Thus the present study concludes that Zn nanoparticles can be used as a potent drug in alternative therapy for treating the cervical cancer patients.

}, keywords = {Abutilon indicum, Cervical cancer, Cytotoxicity, MTT Assay, Zn nanoparticles}, doi = {10.5530/pj.2016.2.5}, author = {Badarinath Druvarao Kulkarni and Samim Sultana and Mayuri Bora and Ishita Dutta and Padmaa Milaap Paarakh and Vedamurthy Ankala Basappa.} } @article {82, title = {Cytotoxicity Study of Ethanol Extract of the Leaves of Asam Kandis (Garcinia cowa Roxb.) on T47D Breast Cancer Cell line}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {Nov-Dec 2015}, pages = {369-371}, type = {Original Article}, chapter = {369}, abstract = {

Objective: To investigate the cytotoxic effect of ethanolic extract of the leaves of asam kandis (Garcinia cowa Roxb.) against T47D breast cancer cells. Methods: The cytotoxicity of ethanol extract was carried out by measuring the activity of mitochondrial dehydrogenase in living cells that have ability to convert dissolved MTT pale yellow to purple formazan product. The extract was added at various concentrations (0.1, 1, 10 and 100 \μg/mL). The level of cytotoxicity was determined by calculating the IC50 value that was based on the percentage of the cell death after 24 hours treatment with the extract. Cell morphological changes were observed by using inverted microscope. Results: The IC50 value showed that ethanol extract of leaves of asam kandis could resist T47D breast cancer cells with IC50 6.13 \± 3.51 \μg/mL. The statistic results proved that ethanol extract of the leaves of asam kandis could inhibit the growth of T47D breast cancer cells significantly at concentrations of 10 \μg/mL and 100 \μg/mL. Conclusion: The results suggest that ethanol extract of the leaves of asam kandis was potential source of herbal medicine for cancer-related ailments.

}, keywords = {Asam kandis, Beast cancer, Cytotoxicity, Garcinia cowa Roxb, MTT Assay, T47D.}, doi = {10.5530/pj.2015.6.9}, author = {Fatma Sri Wahyuni and Dini Hara Triastuti and Helmi Arifin} } @article {1200, title = {Evaluation of Anticancer Potential of Vitus vinifera Seed Against Breast Cancer Cells - MDA-MB-231}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2012}, month = {August 2020}, pages = {1064-1071}, type = {Research Article}, chapter = {1064}, abstract = {

Objective: The aim of the present research is to evaluate the anti-cancer effect of Vitus vinifera seed on MDA-MB-231 cell line. Methods: The Vitus vinifera (Grape) seed were dried, powdered and subjected to methanol, chloroform and ethyl acetate extraction by cold maceration followed by preliminary phytochemical screening. The extracts of Vitus vinifera seed were subjected to assess anti-oxidant status, anti-proliferative activity by MTT assay, GC-MS analysis and apoptotic effect by determining LDH activity on MDA-MB-231. Results: Results indicated that methanolic extract of grape seed showed appreciable anti-oxidant and anti-cancer potential compared with other two extracts. GC-MS mass spectrum of methanolic extract of seed revealed the presence of Dotriacontane, Linoleic acid and Decanoic acid ethyl ester, 1,2,3, propenetriol, monocetate, and Dichloro methyl propane sulfone were detected. Conclusion: The data obtained in this work could be useful as a chemical standard in checking the genuineness of this plant source. Data of the results further depicted that the selected traditional Vitus vinifera seed could be used not only as a potential anti-cancer and good antioxidant.

}, keywords = {GC-MS analysis, MDA-MB-231, MTT Assay, Vitus vinifera seed}, doi = {10.5530/pj.2020.12.150}, author = {Kiruthika Dhanraj and Renuka Saravanan and Sheik Abdulla Shahul Hameed and Sivakumar Ramalingam} }