CYP-450 isoenzymes catalyze the generation of hazardous aromatic amines after reaction with the azo dye Sudan III
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.fct.2013.03.035 http://hdl.handle.net/11449/75764 |
Resumo: | This 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. |
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CYP-450 isoenzymes catalyze the generation of hazardous aromatic amines after reaction with the azo dye Sudan IIIAromatic aminesBiomimetical modelsElectrochemical oxidationIronporphyrinsOxidative metabolismSudan dyes2 methoxy 5 methylaniline2,6 dimethylaniline4 biphenylamine4,4' diaminodiphenyl ether4,4' methylenedianilineanisidinearomatic amineironporphyrinoil scarletporphyrinunclassified drugbase pairingcatalysiselectrochemistryframeshift mutationliquid chromatographymass spectrometrymetabolic activationmutagenic activityoxidationSalmonella typhimuriumThis 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.Faculdade 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, SPInstituto de Química Departamento de Química Analítica Universidade Estadual Paulista - UNESP, Rua Professor Francisco Degni, 55 Quitandinha, 14800-900 Araraquara, SPFaculdade de Filosofia, Ciências e Letras de Ribeirão Preto Departamento de Química Universidade de São Paulo, Av. Bandeirantes 3900, 14040-901 Ribeirão Preto, SPInstituto de Química Departamento de Química Analítica Universidade Estadual Paulista - UNESP, Rua Professor Francisco Degni, 55 Quitandinha, 14800-900 Araraquara, SPUniversidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Zanoni, Thalita BoldrinLizier, Thiago M. [UNESP]Assis, Marilda das DoresZanoni, Maria Valnice Boldrin [UNESP]De Oliveira, Danielle Palma2014-05-27T11:29:48Z2014-05-27T11:29:48Z2013-07-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article217-226application/pdfhttp://dx.doi.org/10.1016/j.fct.2013.03.035Food and Chemical Toxicology, v. 57, p. 217-226.0278-69151873-6351http://hdl.handle.net/11449/7576410.1016/j.fct.2013.03.035WOS:0003204983000282-s2.0-848767993822-s2.0-84876799382.pdf0000-0002-2296-1393Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengFood and Chemical Toxicology3.9771,144info:eu-repo/semantics/openAccess2023-12-25T06:21:28Zoai:repositorio.unesp.br:11449/75764Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:16:14.992738Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
CYP-450 isoenzymes catalyze the generation of hazardous aromatic amines after reaction with the azo dye Sudan III |
title |
CYP-450 isoenzymes catalyze the generation of hazardous aromatic amines after reaction with the azo dye Sudan III |
spellingShingle |
CYP-450 isoenzymes catalyze the generation of hazardous aromatic amines after reaction with the azo dye Sudan III Zanoni, Thalita Boldrin Aromatic amines Biomimetical models Electrochemical oxidation Ironporphyrins Oxidative metabolism Sudan dyes 2 methoxy 5 methylaniline 2,6 dimethylaniline 4 biphenylamine 4,4' diaminodiphenyl ether 4,4' methylenedianiline anisidine aromatic amine ironporphyrin oil scarlet porphyrin unclassified drug base pairing catalysis electrochemistry frameshift mutation liquid chromatography mass spectrometry metabolic activation mutagenic activity oxidation Salmonella typhimurium |
title_short |
CYP-450 isoenzymes catalyze the generation of hazardous aromatic amines after reaction with the azo dye Sudan III |
title_full |
CYP-450 isoenzymes catalyze the generation of hazardous aromatic amines after reaction with the azo dye Sudan III |
title_fullStr |
CYP-450 isoenzymes catalyze the generation of hazardous aromatic amines after reaction with the azo dye Sudan III |
title_full_unstemmed |
CYP-450 isoenzymes catalyze the generation of hazardous aromatic amines after reaction with the azo dye Sudan III |
title_sort |
CYP-450 isoenzymes catalyze the generation of hazardous aromatic amines after reaction with the azo dye Sudan III |
author |
Zanoni, Thalita Boldrin |
author_facet |
Zanoni, Thalita Boldrin Lizier, Thiago M. [UNESP] Assis, Marilda das Dores Zanoni, Maria Valnice Boldrin [UNESP] De Oliveira, Danielle Palma |
author_role |
author |
author2 |
Lizier, Thiago M. [UNESP] Assis, Marilda das Dores Zanoni, Maria Valnice Boldrin [UNESP] De Oliveira, Danielle Palma |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Zanoni, Thalita Boldrin Lizier, Thiago M. [UNESP] Assis, Marilda das Dores Zanoni, Maria Valnice Boldrin [UNESP] De Oliveira, Danielle Palma |
dc.subject.por.fl_str_mv |
Aromatic amines Biomimetical models Electrochemical oxidation Ironporphyrins Oxidative metabolism Sudan dyes 2 methoxy 5 methylaniline 2,6 dimethylaniline 4 biphenylamine 4,4' diaminodiphenyl ether 4,4' methylenedianiline anisidine aromatic amine ironporphyrin oil scarlet porphyrin unclassified drug base pairing catalysis electrochemistry frameshift mutation liquid chromatography mass spectrometry metabolic activation mutagenic activity oxidation Salmonella typhimurium |
topic |
Aromatic amines Biomimetical models Electrochemical oxidation Ironporphyrins Oxidative metabolism Sudan dyes 2 methoxy 5 methylaniline 2,6 dimethylaniline 4 biphenylamine 4,4' diaminodiphenyl ether 4,4' methylenedianiline anisidine aromatic amine ironporphyrin oil scarlet porphyrin unclassified drug base pairing catalysis electrochemistry frameshift mutation liquid chromatography mass spectrometry metabolic activation mutagenic activity oxidation Salmonella typhimurium |
description |
This 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. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-07-01 2014-05-27T11:29:48Z 2014-05-27T11:29:48Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.fct.2013.03.035 Food and Chemical Toxicology, v. 57, p. 217-226. 0278-6915 1873-6351 http://hdl.handle.net/11449/75764 10.1016/j.fct.2013.03.035 WOS:000320498300028 2-s2.0-84876799382 2-s2.0-84876799382.pdf 0000-0002-2296-1393 |
url |
http://dx.doi.org/10.1016/j.fct.2013.03.035 http://hdl.handle.net/11449/75764 |
identifier_str_mv |
Food and Chemical Toxicology, v. 57, p. 217-226. 0278-6915 1873-6351 10.1016/j.fct.2013.03.035 WOS:000320498300028 2-s2.0-84876799382 2-s2.0-84876799382.pdf 0000-0002-2296-1393 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Food and Chemical Toxicology 3.977 1,144 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
217-226 application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808129302565224448 |