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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/75764
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dc.contributor.authorZanoni, Thalita Boldrin-
dc.contributor.authorLizier, Thiago M.-
dc.contributor.authorAssis, Marilda das Dores-
dc.contributor.authorZanoni, Maria Valnice Boldrin-
dc.contributor.authorDe Oliveira, Danielle Palma-
dc.date.accessioned2014-05-27T11:29:48Z-
dc.date.accessioned2016-10-25T18:50:18Z-
dc.date.available2014-05-27T11:29:48Z-
dc.date.available2016-10-25T18:50:18Z-
dc.date.issued2013-07-01-
dc.identifierhttp://dx.doi.org/10.1016/j.fct.2013.03.035-
dc.identifier.citationFood and Chemical Toxicology, v. 57, p. 217-226.-
dc.identifier.issn0278-6915-
dc.identifier.issn1873-6351-
dc.identifier.urihttp://hdl.handle.net/11449/75764-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/75764-
dc.description.abstractThis work describes the mutagenic response of Sudan III, an adulterant food dye, using Salmonella typhimurium assay and the generation of hazardous aromatic amines after different oxidation methods of this azo dye. For that, we used metabolic activation by S9, catalytic oxidation by ironporphyrin and electrochemistry oxidation in order to simulate endogenous oxidation conditions. The oxidation reactions promoted discoloration from 65% to 95% of Sudan III at 1×10-4molL-1 and generation of 7.6×10-7molL-1 to 0.31×10-4molL-1 of aniline, o-anisidine, 2-methoxi-5-methylaniline, 4-aminobiphenyl, 4,4'-oxydianiline; 4,4'-diaminodiphenylmethane and 2,6-dimethylaniline. The results were confirmed by LC-MS-MS experiments. We also correlate the mutagenic effects of Sudan III using S. typhimurium with the strain TA1535 in the presence of exogenous metabolic activation (S9) with the metabolization products of this compound. Our findings clearly indicate that aromatic amines are formed due to oxidative reactions that can be promoted by hepatic cells, after the ingestion of Sudan III. Considering that, the use of azo compounds as food dyestuffs should be carefully controlled. © 2013 Elsevier Ltd.en
dc.format.extent217-226-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAromatic amines-
dc.subjectBiomimetical models-
dc.subjectElectrochemical oxidation-
dc.subjectIronporphyrins-
dc.subjectOxidative metabolism-
dc.subjectSudan dyes-
dc.subject2 methoxy 5 methylaniline-
dc.subject2,6 dimethylaniline-
dc.subject4 biphenylamine-
dc.subject4,4' diaminodiphenyl ether-
dc.subject4,4' methylenedianiline-
dc.subjectanisidine-
dc.subjectaromatic amine-
dc.subjectironporphyrin-
dc.subjectoil scarlet-
dc.subjectporphyrin-
dc.subjectunclassified drug-
dc.subjectbase pairing-
dc.subjectcatalysis-
dc.subjectelectrochemistry-
dc.subjectframeshift mutation-
dc.subjectliquid chromatography-
dc.subjectmass spectrometry-
dc.subjectmetabolic activation-
dc.subjectmutagenic activity-
dc.subjectoxidation-
dc.subjectSalmonella typhimurium-
dc.titleCYP-450 isoenzymes catalyze the generation of hazardous aromatic amines after reaction with the azo dye Sudan IIIen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationFaculdade de Ciências Farmacêuticas de Ribeirão Preto Departamento de Análises Clínicas Toxicológicas e Bromatológicas Universidade de São Paulo, Avenida do Café, s/n, 14040-903 Ribeirão Preto, SP-
dc.description.affiliationInstituto de Química Departamento de Química Analítica Universidade Estadual Paulista - UNESP, Rua Professor Francisco Degni, 55 Quitandinha, 14800-900 Araraquara, SP-
dc.description.affiliationFaculdade de Filosofia, Ciências e Letras de Ribeirão Preto Departamento de Química Universidade de São Paulo, Av. Bandeirantes 3900, 14040-901 Ribeirão Preto, SP-
dc.description.affiliationUnespInstituto de Química Departamento de Química Analítica Universidade Estadual Paulista - UNESP, Rua Professor Francisco Degni, 55 Quitandinha, 14800-900 Araraquara, SP-
dc.identifier.doi10.1016/j.fct.2013.03.035-
dc.identifier.wosWOS:000320498300028-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-84876799382.pdf-
dc.relation.ispartofFood and Chemical Toxicology-
dc.identifier.scopus2-s2.0-84876799382-
dc.identifier.orcid0000-0002-2296-1393-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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