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A stability-indicating LC method for difloxacin in the presence of degradation products

dc.contributor.authorCazedey, Edith Cristina Laignier
dc.contributor.authorJuodinis, Vanessa D'amaro [UNESP]
dc.contributor.authorSalgado, Hérida Regina Nunes [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Federal da Bahia (UFBA)
dc.date.accessioned2016-01-28T16:56:35Z
dc.date.available2016-01-28T16:56:35Z
dc.date.issued2014
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.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.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.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.lattes6258455310334944
dc.identifier.lattes9881720291571774
dc.identifier.urihttp://hdl.handle.net/11449/133781
dc.language.isoeng
dc.relation.ispartofWorld Journal of Pharmacy & Pharmaceutical Sciences
dc.rights.accessRightsAcesso restritopt
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.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscoverye214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.lattes6258455310334944
unesp.author.lattes9881720291571774
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentFármacos e Medicamentos - FCFpt

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