Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/64139
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dc.contributor.authorSiriporn Taokaewen_US
dc.contributor.authorSuratsawadee Piyaviriyakulen_US
dc.contributor.authorPongpun Siripongen_US
dc.contributor.authorMuenduen Phisalaphongen_US
dc.date.accessioned2019-05-07T09:59:49Z-
dc.date.available2019-05-07T09:59:49Z-
dc.date.issued2018en_US
dc.identifier.issn0125-2526en_US
dc.identifier.urihttp://it.science.cmu.ac.th/ejournal/dl.php?journal_id=9143en_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/64139-
dc.description.abstractThe antimicrobial, anticancer and cytotoxic activities of crude extracts of the pericarps of mangosteen fruits, generated using water or ethanol as the extractant, were evaluated and compared with those of a-mangostin. Due to higher total mangostin content in the ethanolic extract (EEM), this extract exhibited considerably stronger activities against pathogenic microbes and skin cancer cells than the aqueous extract (AEM) did. Staphylococcus aureus and Escherichia coli showed high sensitivity to EEM, with minimum inhibitory concentrations (MICs) of 31.25 and 125 mg/ml, respectively. Selected bacteria and fungi exhibited good in vitro susceptibility to EEM, with minimum bactericidal and fungicidal concentrations (MBC and MFC) of less than 0.5 mg/ml. Shrinkage and lysis of bacteria were clearly observed after treatment with EEM or a-mangostin. EEM and a-mangostin also caused swelling and lysis of Candida albicans. EEM showed a great cytotoxic effect on B16F10 murine melanoma cells at 24, 48, and 72 h judged by IC50 values of less than 25 mg/ml, which were 15-100 times lower than IC50 values of AEM, but 4-10 times higher than those of a-mangostin. It was shown that the cell membranes of B16F10 cells were damaged after being treated with EEM and a-mangostin for 24 h.en_US
dc.languageEngen_US
dc.publisherScience Faculty of Chiang Mai Universityen_US
dc.titleAqueous and Ethanolic Extracts of Mangosteen Peels as Natural Antimicrobial/anticancer Materials Against Pathogenic Microbes and B16F10 Murine Melanomaen_US
dc.typeบทความวารสารen_US
article.title.sourcetitleChiang Mai Journal of Scienceen_US
article.volume45en_US
article.stream.affiliationsChemical Engineering Research Unit for Value Adding of Bioresources, Department of Chemical Engineering, Faculty of Engineering, Chulalongkorn University, Bangkok 10330, Thailand.en_US
article.stream.affiliationsNatural Products Research Section, Research Division, National Cancer Institute of Thailand, Bangkok 10400, Thailand.en_US
article.stream.affiliationsDepartment of Materials Science and Technology, Graduate School of Engineering, Nagaoka University of Technology, Niigata 940-2188, Japan.en_US
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