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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/73473
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dc.contributor.authorNwidu, Lucky Lebgosi-
dc.contributor.authorNwafor, Paul Alozie-
dc.contributor.authorVilegas, Wagner-
dc.date.accessioned2014-05-27T11:26:54Z-
dc.date.accessioned2016-10-25T18:37:43Z-
dc.date.available2014-05-27T11:26:54Z-
dc.date.available2016-10-25T18:37:43Z-
dc.date.issued2012-08-01-
dc.identifierhttp://dx.doi.org/10.7324/JAPS.2012.2841-
dc.identifier.citationJournal of Applied Pharmaceutical Science, v. 2, n. 8, p. 233-242, 2012.-
dc.identifier.issn2231-3354-
dc.identifier.urihttp://hdl.handle.net/11449/73473-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/73473-
dc.description.abstractCarpolobia lutea leaves (CLL) (Polygalaceae) were earlier screened and the antiulcer ethnomedicinal claim established. This article seeks to quantitatively isolate, elucidate the active compounds from most active CLL fraction. Fractionation was by semi-preparative HPLC; the active fraction was subjected to radical scavenging assays (RSA) and quantification of the total phenolic content (TPC) were also executed. Results: Ethyl acetate fraction (EAF) was observed to be the most pharmacologically active antiulcer fraction when screened using acute ulcer models induced in rodents. The EAF demonstrated significant (p < 0.05-0.001) antiulcer activity in various in vivo induced ulceration models by reducing the ulcer index and increasing the preventive ratio. The EAF demonstrated > 70% in TPC and < 20 % in RSA. Cinnamic and coumaric acids derivatives were isolated from EAF. Cinnamic acids have been implicated and patented as antiulcer agent. Isolated compounds could in part mediate the observed pharmacological activities which lend credence to its ethnobotanical uses.en
dc.format.extent233-242-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectCarpolobia lutea-
dc.subjectCinnamoyl-
dc.subjectCoumaroyl-1-deoxyglucoside-
dc.subjectPolygalaceae-
dc.subjectUlcerogenic-
dc.titleAntiulcer effects of Ethyl acetate fraction of Carpolobia lutea leafen
dc.typeoutro-
dc.contributor.institutionNiger Delta University-
dc.contributor.institutionUniversity of Uyo-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Pharmacology and Toxicology Faculty of Pharmacy Niger Delta University, P.O.Box 10935, Wilberforce, Island, Bayelsa State-
dc.description.affiliationDepartment of Pharmacology and Toxicology Faculty of Pharmacy University of Uyo, Uyo, Akwa Ibom State, 520003-
dc.description.affiliationDepartment of Organic Chemistry Chemistry Institute São Paulo State University, UNESP-CP 355, CEP 14801-970, Araraquara, SP-
dc.description.affiliationUnespDepartment of Organic Chemistry Chemistry Institute São Paulo State University, UNESP-CP 355, CEP 14801-970, Araraquara, SP-
dc.identifier.doi10.7324/JAPS.2012.2841-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-84876061315.pdf-
dc.relation.ispartofJournal of Applied Pharmaceutical Science-
dc.identifier.scopus2-s2.0-84876061315-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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