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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/16505
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dc.contributor.authorLima Chaves, Carolina de Andrade-
dc.contributor.authorMachado, Ana Lucia-
dc.contributor.authorCarlos, Iracilda Zeppone-
dc.contributor.authorGiampaolo, Eunice Teresinha-
dc.contributor.authorPavarina, Ana Claudia-
dc.contributor.authorVergani, Carlos Eduardo-
dc.date.accessioned2014-05-20T13:46:36Z-
dc.date.accessioned2016-10-25T17:00:17Z-
dc.date.available2014-05-20T13:46:36Z-
dc.date.available2016-10-25T17:00:17Z-
dc.date.issued2010-10-01-
dc.identifierhttp://dx.doi.org/10.1016/j.dental.2010.06.008-
dc.identifier.citationDental Materials. Oxford: Elsevier B.V., v. 26, n. 10, p. 1017-1023, 2010.-
dc.identifier.issn0109-5641-
dc.identifier.urihttp://hdl.handle.net/11449/16505-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/16505-
dc.description.abstractObjectives. The aim of this study was to evaluate the cytotoxic effect of the monomers isobutyl methacrylate (IBMA) and 1,6-hexanediol dimethacrylate (1,6-HDMA), the plasticizer di-n-butyl phthalate (DBP), and the degradation by-products methacrylic acid (MA) and benzoic acid (BA) on L929 cells. Based on previous investigations on the release of these compounds from hard chairside reline resins, a range of concentrations (mu mol/L) were selected for the cytotoxicity tests (IBMA, 5.491406.57; 1,6-HDMA, 1.2239.32; DBP, 1.12143.8; MA, 9.07581; BA, 3.19409).Methods. Cytotoxic effects were assessed using MTT and 3H-thymidine assays after the cells had been exposed to the test compounds at the given concentrations for 24h. Cytotoxicity was rated based on cell viability relative to controls (cells exposed to medium without test substances).Results. DNA synthesis activity was inhibited by all compounds. Mitochondrial dehydrogenase activity decreased in cells treated with monomers, plasticizer and MA by-product, whereas no cytotoxic effect was observed on contact with BA at the majority of concentrations tested. The ranges of suppression for 3H-thymidine assay were: IBMA, 2595%; 1,6-HDMA, 9598%; DBP, 4098%; MA, 9799%; BA, 5471%. For MTT assay, the ranges of suppression were: IBMA, 096%; 1,6-HDMA, 2689%; DBP, 1780%; MA, 5266%; BA, 027%. The 3H-thymidine assay was more sensitive than the MTT assay.Significance. This study evaluated the cytotoxicity of a wide range of concentrations of monomers (IBMA and 1,6-HDMA), plasticizer (DBP) and degradation by-products (MA and BA), including those expected to be released from hard chairside reline resins. The differences observed in the cytotoxicity of these compounds, along with other properties, may assist the dental practitioners in the selection of reline materials with improved service life performance and low risk of adverse reactions in patients who wear relined dentures.en
dc.format.extent1017-1023-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectAcrylic resinsen
dc.subjectCytotoxicityen
dc.subjectMonomeren
dc.subjectPlasticizeren
dc.subjectDegradation productsen
dc.subjectFibroblastsen
dc.titleCytotoxicity of monomers, plasticizer and degradation by-products released from dental hard chairside reline resinsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv Estadual Paulista, UNESP, Araraquara Dent Sch, Dept Dent Mat & Prosthodont, BR-14801903 São Paulo, Brazil-
dc.description.affiliationUniv Estadual Paulista, UNESP, Araraquara Pharmaceut Sch, Dept Clin Anal, BR-14801903 São Paulo, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, UNESP, Araraquara Dent Sch, Dept Dent Mat & Prosthodont, BR-14801903 São Paulo, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, UNESP, Araraquara Pharmaceut Sch, Dept Clin Anal, BR-14801903 São Paulo, Brazil-
dc.identifier.doi10.1016/j.dental.2010.06.008-
dc.identifier.wosWOS:000281349700009-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofDental Materials-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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