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dc.contributor.authorLopes, Cristiani C. G. O.
dc.contributor.authorSalgado, Hérida Regina Nunes [UNESP]
dc.date.accessioned2014-05-20T13:24:49Z
dc.date.available2014-05-20T13:24:49Z
dc.date.issued2010-08-15
dc.identifierhttp://dx.doi.org/10.1016/j.talanta.2010.05.056
dc.identifier.citationTalanta. Amsterdam: Elsevier B.V., v. 82, n. 3, p. 918-922, 2010.
dc.identifier.issn0039-9140
dc.identifier.urihttp://hdl.handle.net/11449/7799
dc.description.abstractLinezolid (LNZ) is one of the first commercially available (and most widely used) oxazolidinone antibiotics. This study describes the development and validation of a microbiological assay, applying the cylinder-plate method, for the determination of the antibiotic linezolid, as well as the evaluation of the ability of the method in determining the stability of linezolid in tablets. The validation method yielded good results and included linearity, precision, accuracy, robustness and selectivity. The assay is based on the inhibitory effect of LNZ upon the strain of Bacillus subtilis ATCC 9372 used as the test microorganism. The results of the assay were treated statistically by analysis of variance (ANOVA) and were found to be linear (r(2) = 0.9998) in the range of 20-80 mu g mL(-1), precise (inter-assay: R.S.D. = 0.61) and accurate (R.S.D. = 1.7). The method developed and validated proved to be indicative of stability and capable of determining the decay of linezolid in the presence of photodegradation products. Comparison of bioassay and liquid chromatography by ANOVA showed no significant difference between methodologies. The results demonstrated the validity of the proposed bioassay, which is a simple and useful alternative methodology for LNZ determination in routine quality control. (C) 2010 Elsevier B.V. All rights reserved.en
dc.description.sponsorshipPACD-FCFAr-UNESP (Araraquara, Brazil)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipFUNDUNEP (São Paulo, Brazil)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.format.extent918-922
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofTalanta
dc.sourceWeb of Science
dc.subjectLinezoliden
dc.subjectBioassayen
dc.subjectPharmaceutical formulationsen
dc.subjectStability solid stateen
dc.titleDevelopment and validation of a stability-indicative agar diffusion assay to determine the potency of linezolid in tablets in the presence of photodegradation productsen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dc.contributor.institutionUniversidade Federal do Ceará (UFC)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.description.affiliationUniversidade Federal do Ceará (UFC), Dept Farm, FFOE, BR-60430370 Fortaleza, Ceara, Brazil
dc.description.affiliationUniv Estadual Paulista, Fac Ciencias Farmaceut, Dept Farmacos & Medicamentos, UNESP, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Fac Ciencias Farmaceut, Dept Farmacos & Medicamentos, UNESP, BR-14801902 Araraquara, SP, Brazil
dc.identifier.doi10.1016/j.talanta.2010.05.056
dc.identifier.wosWOS:000281177100008
dc.rights.accessRightsAcesso restrito
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.author.orcid0000-0002-8120-2362[1]
unesp.author.orcid0000-0002-0385-340X[2]
dc.relation.ispartofjcr4.244
dc.relation.ispartofsjr1,186
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