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CYP-450 isoenzymes catalyze the generation of hazardous aromatic amines after reaction with the azo dye Sudan III

dc.contributor.authorZanoni, Thalita Boldrin
dc.contributor.authorLizier, Thiago M. [UNESP]
dc.contributor.authorAssis, Marilda das Dores
dc.contributor.authorZanoni, Maria Valnice Boldrin [UNESP]
dc.contributor.authorDe Oliveira, Danielle Palma
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:29:48Z
dc.date.available2014-05-27T11:29:48Z
dc.date.issued2013-07-01
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.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.format.extent217-226
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.doi10.1016/j.fct.2013.03.035
dc.identifier.file2-s2.0-84876799382.pdf
dc.identifier.issn0278-6915
dc.identifier.issn1873-6351
dc.identifier.orcid0000-0002-2296-1393
dc.identifier.scopus2-s2.0-84876799382
dc.identifier.urihttp://hdl.handle.net/11449/75764
dc.identifier.wosWOS:000320498300028
dc.language.isoeng
dc.relation.ispartofFood and Chemical Toxicology
dc.relation.ispartofjcr3.977
dc.relation.ispartofsjr1,144
dc.rights.accessRightsAcesso aberto
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.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dspace.entity.typePublication
unesp.author.orcid0000-0002-2296-1393[4]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentQuímica Analítica - IQARpt

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