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http://acervodigital.unesp.br/handle/11449/25849
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DC Field | Value | Language |
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dc.contributor.author | Oliveira, G. A. R. | - |
dc.contributor.author | Ferraz, E. R. A. | - |
dc.contributor.author | Chequer, F. M. D. | - |
dc.contributor.author | Grando, M. D. | - |
dc.contributor.author | Angeli, J. P. F. | - |
dc.contributor.author | Tsuboy, M. S. | - |
dc.contributor.author | Marcarini, J. C. | - |
dc.contributor.author | Mantovani, M. S. | - |
dc.contributor.author | Osugi, M. E. | - |
dc.contributor.author | Lizier, T. M. | - |
dc.contributor.author | Zanoni, Maria Valnice Boldrin | - |
dc.contributor.author | Oliveira, D. P. | - |
dc.date.accessioned | 2014-05-20T14:19:24Z | - |
dc.date.accessioned | 2016-10-25T17:41:03Z | - |
dc.date.available | 2014-05-20T14:19:24Z | - |
dc.date.available | 2016-10-25T17:41:03Z | - |
dc.date.issued | 2010-12-21 | - |
dc.identifier | http://dx.doi.org/10.1016/j.mrgentox.2010.09.001 | - |
dc.identifier.citation | Mutation Research-genetic Toxicology and Environmental Mutagenesis. Amsterdam: Elsevier B.V., v. 703, n. 2, p. 200-208, 2010. | - |
dc.identifier.issn | 1383-5718 | - |
dc.identifier.uri | http://hdl.handle.net/11449/25849 | - |
dc.identifier.uri | http://acervodigital.unesp.br/handle/11449/25849 | - |
dc.description.abstract | The treatment of textile effluents by the conventional method based on activated sludge followed by a chlorination step is not usually an effective method to remove azo dyes, and can generate products more mutagenic than the untreated dyes. The present work evaluated the efficiency of conventional chlorination to remove the genotoxicity/mutagenicity of the azo dyes Disperse Red 1, Disperse Orange 1, and Disperse Red 13 from aqueous solutions. The comet and micronucleus assays with HepG2 cells and the Salmonella mutagenicity assay were used. The degradation of the dye molecules after the same treatment was also evaluated, using ultraviolet and visible absorption spectrum measurements (UV-vis), high performance liquid chromatography coupled to a diode-array detector (HPLC-DAD), and total organic carbon removal (TOC) analysis. The comet assay showed that the three dyes studied induced damage in the DNA of the HepG2 cells in a dose-dependent manner. After chlorination, these dyes remained genotoxic, although with a lower damage index (DI). The micronucleus test showed that the mutagenic activity of the dyes investigated was completely removed by chlorination, under the conditions tested. The Salmonella assay showed that chlorination reduced the mutagenicity of all three dyes in strain YG1041, but increased the mutagenicity of Disperse Red 1 and Disperse Orange 1 in strain TA98. With respect to chemical analysis, all the solutions showed rapid discoloration and a reduction in the absorbance bands characteristic of the chromophore group of each dye. However, the TOC was not completely removed, showing that chlorination of these dyes is not efficient in mineralizing them. It was concluded that conventional chlorination should be used with caution for the treatment of aqueous samples contaminated with azo dyes. (C) 2010 Elsevier B.V. All rights reserved. | en |
dc.description.sponsorship | Faculdade de Ciencias Farmaceuticas de Ribeirao Preto | - |
dc.description.sponsorship | Universidade de São Paulo | - |
dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | - |
dc.description.sponsorship | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) | - |
dc.format.extent | 200-208 | - |
dc.language.iso | eng | - |
dc.publisher | Elsevier B.V. | - |
dc.source | Web of Science | - |
dc.subject | Azo dye | en |
dc.subject | Chlorination | en |
dc.subject | Comet assay | en |
dc.subject | Micronucleus assay | en |
dc.subject | Salmonella assay | en |
dc.title | Chlorination treatment of aqueous samples reduces, but does not eliminate, the mutagenic effect of the azo dyes Disperse Red 1, Disperse Red 13 and Disperse Orange 1 | en |
dc.type | outro | - |
dc.contributor.institution | Universidade de São Paulo (USP) | - |
dc.contributor.institution | Universidade Estadual de Londrina (UEL) | - |
dc.contributor.institution | Universidade Estadual Paulista (UNESP) | - |
dc.description.affiliation | Univ São Paulo, Dept Anal Clin Toxicol & Bromatol, Fac Ciencias Farmaceut Ribeirao Preto, USP, BR-14040903 Ribeirao Preto, SP, Brazil | - |
dc.description.affiliation | Universidade Estadual de Londrina (UEL), Dept Biol Geral, Ctr Ciencias Biol, UEL, BR-86061990 Londrina, PR, Brazil | - |
dc.description.affiliation | Univ Estadual Paulista, UNESP, Inst Quim Araraquara, Dept Quim Analit, BR-14800900 Araraquara, SP, Brazil | - |
dc.description.affiliationUnesp | Univ Estadual Paulista, UNESP, Inst Quim Araraquara, Dept Quim Analit, BR-14800900 Araraquara, SP, Brazil | - |
dc.identifier.doi | 10.1016/j.mrgentox.2010.09.001 | - |
dc.identifier.wos | WOS:000285865400018 | - |
dc.rights.accessRights | Acesso restrito | - |
dc.relation.ispartof | Mutation Research: Genetic Toxicology and Environmental Mutagenesis | - |
dc.identifier.orcid | 0000-0002-2296-1393 | - |
Appears in Collections: | Artigos, TCCs, Teses e Dissertações da Unesp |
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