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The effect of rifampicin and pyrazinamide on isoniazid pharmacokinetics in rats

dc.contributor.authorBaldan, Helen M. [UNESP]
dc.contributor.authorDe Rosa, Helene J. [UNESP]
dc.contributor.authorBrunetti, Iguatemy Lourenço [UNESP]
dc.contributor.authorXimenes, Valdecir Farias [UNESP]
dc.contributor.authorMachado, Rosangela G. P. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:24:37Z
dc.date.available2014-05-20T13:24:37Z
dc.date.issued2007-11-01
dc.description.abstractTuberculosis chemotherapy involves combination of the drugs isoniazid (INH), rifampicin (RMP) and pyrazinamide (PYR) for a 6-month period. The present work investigated the influence of RMP and PYR on the pharmacokinetic parameters of INH when groups of rats were pre-treated for 21 days with INH alone or in combination with RMP and/or PYR, in the following amounts per kg body weight: INH 100 mg; INH 100 mg + RMP 100 mg; INH 100 mg + PYR 350 mg; INH 100 mg + PYR 350 mg + RMP 100 mg. It was found that the co-administration of PYR caused an increase in the INH distribution volume (V-d/F), half-life of elimination t(1)/2(beta)) and clearance (Cl-T/F), and a decrease in the area under curve 0 to 24 h (AUC). Co-administration of RMP caused an increase in the Cl-T/F and a decrease in the AUC. The combination INH + PYR + RMP caused an increase in the Cl-T/F and a decrease in the AUC. These significant pharmacokinetic interactions between the tuberculostatic drugs might be related to differences in the therapeutic and toxic effects. Copyright 0( 2007 John Wiley & Sons, Ltd.en
dc.description.affiliationUniv Estadual Paulista, Fac Ciências Farmaceut, Dept Principios Ativos Nat, Araraquara, SP, Brazil
dc.description.affiliationUniv Estadual Paulista, Fac Ciências Farmaceut, Dept Analises Clinicas, Araraquara, SP, Brazil
dc.description.affiliationUniv Estadual Paulista, Fac Ciências, Dept Quim, Bauru, SP, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Fac Ciências Farmaceut, Dept Principios Ativos Nat, Araraquara, SP, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Fac Ciências Farmaceut, Dept Analises Clinicas, Araraquara, SP, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Fac Ciências, Dept Quim, Bauru, SP, Brazil
dc.format.extent409-413
dc.identifierhttp://dx.doi.org/10.1002/bdd.570
dc.identifier.citationBiopharmaceutics & Drug Disposition. Chichester: John Wiley & Sons Ltd, v. 28, n. 8, p. 409-413, 2007.
dc.identifier.doi10.1002/bdd.570
dc.identifier.issn0142-2782
dc.identifier.lattes4066413997908572
dc.identifier.urihttp://hdl.handle.net/11449/7692
dc.identifier.wosWOS:000251955200001
dc.language.isoeng
dc.publisherWiley-Blackwell
dc.relation.ispartofBiopharmaceutics & Drug Disposition
dc.relation.ispartofjcr1.677
dc.relation.ispartofsjr0,551
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectpharmacokineticspt
dc.subjectisoniazidpt
dc.subjectpyrazinamidept
dc.subjectrifampicinpt
dc.titleThe effect of rifampicin and pyrazinamide on isoniazid pharmacokinetics in ratsen
dc.typeArtigopt
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dcterms.rightsHolderWiley-Blackwell
dspace.entity.typePublication
relation.isDepartmentOfPublicationa83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isDepartmentOfPublication.latestForDiscoverya83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.lattes4066413997908572
unesp.author.orcid0000-0003-2636-3080[4]
unesp.author.orcid0000-0003-4927-7599[3]
unesp.author.orcid0000-0002-2692-8101[5]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências, Baurupt
unesp.departmentQuímica - FCpt
unesp.departmentAnálises Clínicas - FCFpt

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