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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/130910
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dc.contributor.authorSantos, Jean L.-
dc.contributor.authorBosquesi, Priscila L.-
dc.contributor.authorAlmeida, Adélia E.-
dc.contributor.authorChin, Chung Man-
dc.contributor.authorVaranda, Eliana A.-
dc.date.accessioned2015-12-07T15:30:07Z-
dc.date.accessioned2016-10-25T21:22:17Z-
dc.date.available2015-12-07T15:30:07Z-
dc.date.available2016-10-25T21:22:17Z-
dc.date.issued2011-
dc.identifierhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614842/-
dc.identifier.citationInternational Journal Of Biomedical Science : Ijbs, v. 7, n. 4, p. 263-267, 2011.-
dc.identifier.issn1550-9702-
dc.identifier.urihttp://hdl.handle.net/11449/130910-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/130910-
dc.description.abstractThe hydroxyurea, a cytotoxic drug, is the mainly available therapeutical strategy for the treatment of sickle cell disease. This study aimed to evaluate the mutagenic and genotoxic potential of the hydroxyurea through the Salmonella/Microsome assay and micronucleus test in peripheral blood of mice. The doses were evaluated at 29.25-468 μmol/plate in Salmonella/Microsome assay in presence and absence of metabolic activation the drug. In the micronucleus test the doses were evaluated at 12.5; 25; 50; 75 and 100 mg/kg. The results show that hydroxyurea present mutagenic activity in TA98 and TA100 in doses above 117 μmol/plate and 234 μmol/plate respectively. The drug induced a significant increase in the frequency of micronuclei in reticulocytes of mice at concentrations of 50, 75 and 100 mg/kg, compared to negative control (water). These results demonstrated the mutagenic and genotoxic potential of hydroxyurea.en
dc.format.extent263-267-
dc.language.isoeng-
dc.publisherInternational Journal Of Biomedical Science : Ijbs-
dc.sourcePubMed-
dc.subjectGenotoxicityen
dc.subjectHydroxyureaen
dc.subjectMicronucleus testen
dc.subjectMutagenicityen
dc.titleMutagenic and genotoxic effect of hydroxyureaen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationLapdesf - Laboratório de Pesquisa e Desenvolvimento de Fármacos. Departamento de Fármacos e Medicamentos - Faculdade de Ciências Farmacêuticas - Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP) Rodovia Araraquara-Jaú Km.01 s/n, 14801-902, Araraquara, São Paulo, Brasil;-
dc.description.affiliationUnespLapdesf - Laboratório de Pesquisa e Desenvolvimento de Fármacos. Departamento de Fármacos e Medicamentos - Faculdade de Ciências Farmacêuticas - Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP) Rodovia Araraquara-Jaú Km.01 s/n, 14801-902, Araraquara, São Paulo, Brasil;-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofInternational Journal Of Biomedical Science : Ijbs-
dc.identifier.pubmed23675245-
dc.identifier.pmcPMC3614842-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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