<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Manggiasih Dwiayu Larasati</style></author><author><style face="normal" font="default" size="100%">Silvia W. Lestari</style></author><author><style face="normal" font="default" size="100%">Mulyoto Pangestu</style></author><author><style face="normal" font="default" size="100%">Andon Hestiantoro</style></author><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Effect of Cryopreservation on the Sperm Ultrastructure of Mus Musculus Albinus Strain DDY: Comparison of Nakagata vs Modified vs Kitazato Cryoprotectants</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">cryopreservation</style></keyword><keyword><style  face="normal" font="default" size="100%">glycerol</style></keyword><keyword><style  face="normal" font="default" size="100%">mice sperm</style></keyword><keyword><style  face="normal" font="default" size="100%">raffinose</style></keyword><keyword><style  face="normal" font="default" size="100%">Scanning electron microscope</style></keyword><keyword><style  face="normal" font="default" size="100%">Trehalose</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">563-569</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Sperm morphology analysis is very necessary to understand male fertility and the etiology of infertility. Currently, scanning electron microscopy (SEM) has been widely used to determine surface topology. In this study, we will compare the effects of spermatozoa cryopreservation using three different types of cryoprotectants, namely Nakagata, modification and Kitazato. The cryoprotectant compositions used are Nakagata (raffinose and skim milk), modified (glycerol and raffinose) and Kitazato (glycerol and trehalose). &lt;strong&gt;Methods:&lt;/strong&gt; SEM analysis was carried out on 8 sperm samples before cryopreservation and after the freeze-thaw process. &lt;strong&gt;Results:&lt;/strong&gt; The results obtain showed that cryoprotectant modification was able to protect spermatozoa morphology better than Nakagata and Kitazato. Analysis revealed damage to plasma membrane, acrosome and loss of mitochondria in all treatment groups compared to fresh sperm. SEM showed obvious signs of post-thaw damage such as missing plasma membranes, sperm showing damaged acrosomes and mitochondria in the middle showing structural disorganization. &lt;strong&gt;Conclusion: &lt;/strong&gt;SEM revealed that cryopreservation caused ultrastructural damage to mice sperm due to freezing and thawing. These details provide valuable data for further research to minimize the damage caused by cryopreservation to mice sperm. Apart from that, further examination using TEM is recommended to obtain a more comprehensive picture.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">563</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Manggiasih Dwiayu Larasati&lt;sup&gt;1&lt;/sup&gt;, Silvia W. Lestari&lt;sup&gt;2&lt;/sup&gt;,* Mulyoto Pangestu&lt;sup&gt;3&lt;/sup&gt;, Andon Hestiantoro&lt;sup&gt;4&lt;/sup&gt;, Kusmardi Kusmardi&lt;sup&gt;5-7&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Doctoral Program in Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya No. 6, Jakarta 10430 INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Medical Biology, Faculty of Medicine, Universitas Indonesia, Jakarta 10430 INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Education Program in Reproduction and Development, Department of Obstetrics and Gynecology, School of Clinical Sciences, Monash University, Victoria, AUSTRALIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, Faculty of Medicine, Universitas Indonesia, Jakarta 10430 INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Pathological Anatomy, Faculty of Medicine, Universitas Indonesia, Jalan Salemba Raya No. 6, Jakarta 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Drug Development Research Center, Indonesia Medical Education and Research Institute (IMERI), Universitas Indonesia, Jalan Salemba Raya No. 6, Jakarta 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Human Cancer Research Center, Indonesia Medical Education and Research Institute (IMERI), Universitas Indonesia, Jalan Salemba Raya No. 6, Jakarta 10430, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Taufiq MMJ</style></author><author><style face="normal" font="default" size="100%">Darah I</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Biological Activity of Lasiodiplodia pseudotheobromae IBRL OS- 64 Extracts, an Endophytic Fungus Isolated from Medicinal Herb, Ocimum sanctum Against Foodborne Diarrhea-Caused Bacteria</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Foodborne disease</style></keyword><keyword><style  face="normal" font="default" size="100%">Lasiodiplodia pseudotheobromae</style></keyword><keyword><style  face="normal" font="default" size="100%">Minimum bactericidal concentration</style></keyword><keyword><style  face="normal" font="default" size="100%">Minimum inhibitory concentration</style></keyword><keyword><style  face="normal" font="default" size="100%">Scanning electron microscope</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">897-904</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Foodborne disease is a serious public health problem worldwide and most of the disease is related to food spoilage by bacteria. Thus, there is a need for the discovery of a natural antibiotic to inhibit these foodborne bacteria. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;Disk diffusion and broth microdilution assays were performed to access the antibacterial activity of the fungal extracts against test bacteria. Meanwhile, the scanning electron microscope (SEM) was employed to study the structural degeneration of bacterial cells exposed to the extracts. &lt;strong&gt;Results: &lt;/strong&gt;The ethyl acetate extract of &lt;em&gt;Lasiodiplodia pseudotheobromae&lt;/em&gt; IBRL OS- 64 demonstrated favorable antibacterial activity towards all test bacteria with inhibition zone ranged from 15.0 mm to 26.0 mm. All test bacteria were resistant to hexane and butanolic extracts. Minimum inhibition concentration (MIC) values of the ethyl acetate extract between 62.5 μg/mL to 500 μg/mL whereas minimum bactericidal concentration (MBC) was in the range of 125 μg/mL to 2000 μg/mL. The SEM micrographs exhibited major abnormalities that occurred on the bacterial cells after exposure to the extract with alteration in their morphology and cell death beyond repair. &lt;strong&gt;Conclusion:&lt;/strong&gt; The extracts of &lt;em&gt;L. pseudotheobromae&lt;/em&gt; IBRL OS-64 may be an effective antibacterial agent to treat foodborne bacteria.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">897</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Taufiq MMJ*, Darah I&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Industrial Biotechnology Research Laboratory, School of Biological Sciences, Universiti Sains Malaysia, 11800 Minden, Penang, MALAYSIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Astha Pandey</style></author><author><style face="normal" font="default" size="100%">Shalvi Agrawal</style></author><author><style face="normal" font="default" size="100%">Amruta D Patel</style></author><author><style face="normal" font="default" size="100%">Dushyant Pendarkar</style></author><author><style face="normal" font="default" size="100%">Jalpa D Bambhaniya</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evergreen Conventional and Modern Microscopic Methods for Solving Various Cases of Forensic Botany by Morphological and Histological Study</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Botanical evidences</style></keyword><keyword><style  face="normal" font="default" size="100%">Cannabis sativa</style></keyword><keyword><style  face="normal" font="default" size="100%">Papaver somniferum</style></keyword><keyword><style  face="normal" font="default" size="100%">Ricinus communis</style></keyword><keyword><style  face="normal" font="default" size="100%">Scanning electron microscope</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">171-176</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The study concerning forensic evidences commences from the physical examination. Microscopic examination serves a good preliminary technique and provides a relatively quick and non-destructive means of obtaining qualitative information without much sample preparation. Various plants or plant materials such as pollens at the crime scene or a rare plant type present near a murder victim can be helpful in connecting suspect to a victim or scene. For examination of such evidences, the initial step is the identification of collected botanical evidences. Scanning electron microscope (SEM) produces images that rely on secondary electrons image and is concerned primarily with the observation of surface topography. SEM images at all direction (X-Y-Z rotation) giving a three dimensional view of the sample under study. &lt;strong&gt;Methods:&lt;/strong&gt; For morphological and histological examination, compound microscope and SEM has been used. Three plant specimens have been taken i.e. &lt;em&gt;Cannabis sativa&lt;/em&gt;,&lt;em&gt; Ricinus communis&lt;/em&gt; and &lt;em&gt;Papaver somniferum&lt;/em&gt;. For compound microscopic examination, sample has been stained with saffranin dye and for SEM examination; sample surface has been coated with gold-palladium layer to make it conductive.&lt;strong&gt; Results:&lt;/strong&gt; The morphological and histological examination by compound microscope and SEM revealed many characteristic features like ellipsoidal pollens in &lt;em&gt;Ricinus&lt;/em&gt;, cystolythic trichomes in &lt;em&gt;Cannabis&lt;/em&gt;, large oval stomata in poppy, etc. &lt;strong&gt;Conclusion:&lt;/strong&gt; The microscopic examination of botanical evidences by such sophisticated technique like SEM holds a lot of scope in forensic investigations with minimal evidence destruction and maximum details can be obtained in a preliminary examination only without using other complicated techniques.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">171</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Astha Pandey&lt;sup&gt;1,&lt;/sup&gt;*, Shalvi Agrawal&lt;sup&gt;2&lt;/sup&gt;, Amruta D Patel&lt;sup&gt;2&lt;/sup&gt;, Dushyant Pendarkar&lt;sup&gt;2&lt;/sup&gt;, Jalpa D Bambhaniya&lt;sup&gt;2&lt;/sup&gt;. &lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Assistant Professor, Institute of Forensic Science Gujarat Forensic Sciences University Sector 9, near DFS office, Gandhinagar 382009- Gujarat, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Research Scholar, Institute of Forensic Science, Gujarat Forensic Sciences University, Gujarat, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Parichat Phalanisong</style></author><author><style face="normal" font="default" size="100%">Kanit Vichitphan</style></author><author><style face="normal" font="default" size="100%">Jaehong Han</style></author><author><style face="normal" font="default" size="100%">Sukanda Vichitphan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">High Antioxidant and Phenolic Contents Related to Antibacterial Activity against Gastrointestinal Pathogenic Bacteria of Some Thai Medicinal Plants</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antibacterial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">antioxidant activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Caesalpinia sappan</style></keyword><keyword><style  face="normal" font="default" size="100%">Scanning electron microscope</style></keyword><keyword><style  face="normal" font="default" size="100%">total phenolic content</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/488</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">341-348</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; Thai medicinal plants were used as the traditional medicines and as part of everyday plants diet. Plants contain a mixture of phytochemical and exhibit a lot of functional food and medicinal properties. This project aims to investigate the potential of selected Thai medicinal plants according to the properties of their antioxidant and antibacterial activities. &lt;strong&gt;Methods:&lt;/strong&gt; The eighteen plants were extracted using maceration method with 95% ethanol. The antioxidant activity was evaluated by DPPH and FRAP assay. The total phenolic content was evaluated by Folin-Ciocalteu phenol reagent. The antibacterial activity was evaluated by agar disc diffusion method. The extract which exhibited high antioxidant and antibacterial activity was selected to observe morphological changes by the scanning electron microscope (SEM). &lt;strong&gt;Results:&lt;/strong&gt; The extract of &lt;em&gt;Caesalpinia sappan&lt;/em&gt; showed the highest activities on both antioxidant assayed by FRAP method and total phenolic contents, however, exhibited high antioxidant assayed by DPPH compared to &lt;em&gt;Bauhinia strychnifolia&lt;/em&gt; extract. Moreover, the extract of &lt;em&gt;C. sappan&lt;/em&gt; showed the excellent antibacterial activities against six pathogenic bacteria in Gastro-intestinal tract. The morphological change by SEM was selected for further investigation antibacterial activities of &lt;em&gt;C. sappan&lt;/em&gt; extract. The results showed that the inhibitory effect to those bacterial strains could be caused by the disruption of the cell membrane and decrease biofilm formation after treatment with the extract. &lt;strong&gt;Conclusion:&lt;/strong&gt; The ethanol extract of &lt;em&gt;C. sappan&lt;/em&gt; exhibited strong antioxidant and antibacterial activities against the six pathogenic bacteria. This result suggested that &lt;em&gt;C. sappan&lt;/em&gt; could be applied to use for medicinal purpose and functional products.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">341</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Parichat Phalanisong&lt;sup&gt;1,2,&lt;/sup&gt; Kanit Vichitphan&lt;sup&gt;2,3&lt;/sup&gt;*, Jaehong Han&lt;sup&gt;4&lt;/sup&gt;, Sukanda Vichitphan&lt;sup&gt;2,3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Graduate School, Khon Kaen University, Khon Kaen, THAILAND.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biotechnology, Faculty of Technology, Khon Kaen University, Khon Kaen, THAILAND.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Fermentation Research Center for Value Added Agricultural Products (FerVAAP), Khon Kaen University, Khon Kaen, THAILAND.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Integrative Plant Science, Chung-Ang University, Anseong, KOREA.&lt;/p&gt;</style></auth-address></record></records></xml>