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dc.contributor.authorAlam, M. Badrul
dc.contributor.authorHossain, M. Sarowar
dc.contributor.authorChowdhury, Nargis Sultana
dc.contributor.authorMazumder, M. Ehsanul Haque
dc.contributor.authorHaque, M. Ekramul
dc.contributor.authorIslam, Anwarul
dc.date.accessioned2016-12-07T04:33:17Z
dc.date.available2016-12-07T04:33:17Z
dc.date.issued2011
dc.identifier.citationBadrul Alam, M., Sarowar Hossain, M., Chowdhury, N. S., Ehsanul Haque Mazumder, M., Ekramul Haque, M., & Islam, A. (2011). In vitro and in vivo antioxidant and toxicity evaluation of different fractions of oxalis corniculata linn. Journal of Pharmacology and Toxicology, 6(4), 337-348. doi:10.3923/jpt.2011.337.348en_US
dc.identifier.issn1816496X
dc.identifier.urihttp://hdl.handle.net/10361/7138
dc.descriptionThis article was published in Journal of Pharmacology and Toxicology [© 2011 Academeic Journals Inc.] and the definite version is available at: http://docsdrive.com/pdfs/academicjournals/jpt/2011/337-348.pdfen_US
dc.description.abstractIn course of investigation on natural antioxidants, the present study was aimed to report the antioxidant activities, both in vitro and in vivo, of the crude methanolic extracts of the whole plant of Oxalis corniculata Linn along with its various organic fractions. The different assay methods, including total antioxidant activity, scavenging free radical, authentic peroxynitrite, nitric oxide and reducing power assessment were used to evaluate the antioxidant potential of the crude extract and its organic fractions. The ethylacetate (EtOAc) fraction, showed strong activity in all the model systems tested and in peroxynitrite model this fraction (IC50 value of 2.29±0.18 μg mL-1) exerted three-fold stronger activity than standard penicillamine (IC50 value of 6.20±0.32 μg mL-1). The reducing power of the extract was found to be concentration dependent. The administration of the extract/fractions at a dose of 250 and 500 mg kg-1 body weight to the male Wistar rats increased the percentage inhibition of reduced glutathione, superoxide dismutase and catalase significantly. Whereas, lipid peroxidation level in hepatotoxic rats markedly decreased at a dose of 500 mg kg-1 body weight after 7 days. The total phenol and flavonoid content were also measured in the crude extract along with its organic fractions. The Brine shrimp lethality bioassay was used to determine the toxicity of the extracts and Vincristin sulphate was used as positive control. The dichloromethane (CH2Cl2) fraction showed highest activity (LC50 value of 29.02±1.16 μg mL-1) and other showed activity in the order of: EtOAc fraction >n-BuOH fraction > MeOH extract > aqueous fraction. Taken together, these results suggest that O. corniculata extract has strong antioxidant properties and further validate the traditional use of this plant.en_US
dc.language.isoenen_US
dc.publisher© 2011 Academeic Journals Inc.en_US
dc.relation.urihttp://scialert.net/abstract/?doi=jpt.2011.337.348
dc.subjectAntioxidant enzymeen_US
dc.subjectFree radicalen_US
dc.subjectOxalis corniculataen_US
dc.subjectPhenolic contenten_US
dc.titleIn vitro and in vivo antioxidant and toxicity evaluation of different fractions of oxalis corniculata linnen_US
dc.typeArticleen_US
dc.description.versionPublished
dc.contributor.departmentDepartment of Pharmacy, BRAC University
dc.identifier.doihttp://doi.org/10.3923/jpt.2011.337.348


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