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dc.contributor.authorAl-Massarani, Shaza-
dc.contributor.authorEl-Sayed, Mohamed-I Kotb-
dc.contributor.authorEl-Shaibany, Amina-
dc.date.accessioned2022-10-26T10:11:35Z-
dc.date.available2022-10-26T10:11:35Z-
dc.date.issued2019-09-16-
dc.identifier.citationAl-Massarani, S., El-Sayed, M. I. K., & El-Shaibany, A. (2019). Antioxidant and anti-proliferative activities of Acalypha fruticosa: Possible elucidated mechanism. Pakistan Journal of Pharmaceutical Sciences, 32(5).en_US
dc.identifier.issn1011-601X-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/13765-
dc.description.abstractThis study aimed to investigate the potential anti-oxidant activity of methanol (Aca-M) extract and n-hexane (Aca-H), chloroform (Aca-Ch), ethyl acetate (Aca-E), n-butanol (Aca-B) and aqueous (Aca-A) fractions obtained from the aerial parts of Acalypha fruticosa (Aca) using the 2, 2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging assay. Data obtained revealed that A. fruticosa methanol extract and different fractions inhibited the DPPH radicals in the following descending order: Aca-E ˃Aca-B ˃Aca-M ˃Aca-A ˃Aca-Ch ˃Aca-H compared to ascorbic acid. Additionally, in vitro 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium (MTT) assay against MCF-7, HCT-116, HepG-2 and noncancerous MRC-5 cell lines was performed to determine their selective anti-cancer activity. The Aca-Ch fraction exhibited remarkable cytotoxic activity against all tested cancerous cell lines with IC50 4.81- 12.2μg/mL, while both AcaCh and Aca-H fractions possessed potent cytotoxic activities on HCT-116 (IC50 4.81 and 10.1, respectively) with negligible harm but selective effect on non-cancerous MRC-5 cells (IC50 20.4 and 85.2, respectively).en_US
dc.language.isoen_USen_US
dc.subjectAcalypha fruticosaen_US
dc.subjectantioxidanten_US
dc.subjectcell linesen_US
dc.subjectcytotoxicityen_US
dc.subjectantiproliferativeen_US
dc.subjectapoptosisen_US
dc.titleAntioxidant and anti-proliferative activities of Acalypha fruticosa: Possible elucidated mechanismen_US
dc.typeArticleen_US
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