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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/133781
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dc.contributor.authorCazedey, Edith Cristina Laignier-
dc.contributor.authorJuodinis, Vanessa D'amaro-
dc.contributor.authorSalgado, Hérida Regina Nunes-
dc.date.accessioned2016-01-28T16:56:35Z-
dc.date.accessioned2016-10-25T21:28:52Z-
dc.date.available2016-01-28T16:56:35Z-
dc.date.available2016-10-25T21:28:52Z-
dc.date.issued2014-
dc.identifierhttp://www.wjpps.com/wjpps_controller/abstract_id/1922-
dc.identifier.citationWorld Journal of Pharmacy & Pharmaceutical Sciences, v. 3, n. 9, p. 45-56, 2014.-
dc.identifier.issn2278-4357-
dc.identifier.urihttp://hdl.handle.net/11449/133781-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/133781-
dc.description.abstractA novel stability-indicating reversed-phase liquid chromatographic (LC) method for the determination of difloxacin (DI) in coated tablets in the presence of degradation products is described. The method was developed using isocratic mode on a reversed-phase C18 column (250 x 4.6 mm id, 5 μm particle size). The mobile phase containing a mixture of 5% acetic acid-methanol (70: 30, v/v) was pumped at a constant flow rate of 1.0 mL/min. The eluted compounds were monitored at 276 nm. DI was subjected to the stress conditions of oxidative, acid, base, hydrolytic, thermal and photolytic degradation. DI was found to degrade significantly in oxidative, acid and base degradation conditions and mildly in hydrolytic degradation conditions and stable in thermal and photolytic degradation conditions. All degradation products were well resolved from the main peak providing the stability-indicating power of the method. The developed method was validated as per International Conference on Harmonization (ICH) guidelines with respect to specificity, limit of detection, limit of quantitation, precision, linearity, accuracy, robustness and system suitability.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.format.extent45-56-
dc.language.isoeng-
dc.sourceCurrículo Lattes-
dc.subjectLiquid chromatographyen
dc.subjectDifloxacinen
dc.subjectStability-indicating methoden
dc.subjectPharmaceutical analysisen
dc.subjectValidationen
dc.titleA stability-indicating LC method for difloxacin in the presence of degradation productsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal da Bahia (UFBA)-
dc.description.affiliationUniversidade Estadual Paulista Júlio de Mesquita Filho, Departamento de Fármacos e Médicamentos, Faculdade de Ciências Farmacêuticas de Araraquara, Araraquara, Rodovia Araraquara-Jaú, km1, Campus, CEP 14801-902, SP, Brasil-
dc.description.affiliationFaculty of Pharmacy, Federal University of Bahia, Salvador, Bahia, Brazil-
dc.description.affiliationUnespUniversidade Estadual Paulista Júlio de Mesquita Filho, Departamento de Fármacos e Médicamentos, Faculdade de Ciências Farmacêuticas de Araraquara, Araraquara, Rodovia Araraquara-Jaú, km1, Campus, CEP 14801-902, SP, Brasil-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofWorld Journal of Pharmacy & Pharmaceutical Sciences-
dc.identifier.lattes9881720291571774-
dc.identifier.lattes6258455310334944-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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