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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/125479
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dc.contributor.authorHebling, Josimeri-
dc.contributor.authorBianchi, L.-
dc.contributor.authorBasso, F. G.-
dc.contributor.authorScheffel, D. l.-
dc.contributor.authorSoares, D. G.-
dc.contributor.authorCarrilho, M. R. O.-
dc.contributor.authorPashley, D. H.-
dc.contributor.authorTjäderhane, L.-
dc.contributor.authorCosta, C. A. de Souza-
dc.date.accessioned2015-08-06T16:12:12Z-
dc.date.accessioned2016-10-25T20:52:59Z-
dc.date.available2015-08-06T16:12:12Z-
dc.date.available2016-10-25T20:52:59Z-
dc.date.issued2015-
dc.identifierhttp://www.sciencedirect.com/science/article/pii/S0109564115000214-
dc.identifier.citationDental Materials, v. 31, n. 4, p. 399-405, 2015.-
dc.identifier.issn0109-5641-
dc.identifier.urihttp://hdl.handle.net/11449/125479-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/125479-
dc.description.abstractTo evaluate the cytotoxicity of dimethyl sulfoxide (DMSO) on the repair-related activity of cultured odontoblast-like MDPC-23 cells. Methods Solutions with different concentrations of DMSO (0.05, 0.1, 0.3, 0.5 and 1.0 mM), diluted in culture medium (DMEM), were placed in contact with MDPC-23 cells (5 × 104 cells/cm2) for 24 h. Eight replicates (n = 8) were prepared for each solutions for the following methods of analysis: violet crystal dye for cell adhesion (CA), quantification of total protein (TP), alizarin red for mineralization nodules formation (MN) and cell death by necrosis (flow cytometry); while twelve replicates (n = 12) were prepared for viable cell number (Trypan Blue) and cell viability (MTT assay). Data were analyzed by ANOVA and Tukey or Kruskal–Wallis and Mann–Whitney's tests (p < 0.05). Results Cell viability, adhesion and percentage of cell death by necrosis were not affected by DMSO at any concentration, with no statistical significant difference among the groups. A significant reduction in total protein production was observed for 0.5 and 1.0 mM of DMSO compared to the control while increased mineralized nodules formation was seen only for 1.0 mM DMSO. Significance: DMSO caused no or minor cytotoxic effects on the pulp tissue repair-related activity of odontoblast-like cells.en
dc.format.extent399-405-
dc.language.isoeng-
dc.sourceCurrículo Lattes-
dc.subjectDimethyl sulfoxideen
dc.subjectCytotoxicityen
dc.subjectOdontoblast-like cellsen
dc.titleCytotoxicity of dimethyl sulfoxide (DMSO) in direct contact with odontoblast-like cellsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Anhanguera de São Paulo-
dc.contributor.institutionGeorgia Regents University College of Dental Medicine-
dc.contributor.institutionUniversity of Oulu-
dc.description.affiliationDepartment of Oral Biology-
dc.description.affiliationUnespUniversidade Estadual Paulista Júlio de Mesquita Filho, Departamento de Clínica Infantil, Faculdade de Odontologia de Araraquara, Araraquara, Rua Humaitá, 1680, Centro, CEP 14801-903, SP, Brasil-
dc.identifier.doihttp://dx.doi.org/10.1016/j.dental.2015.01.007-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofDental Materials-
dc.identifier.lattes8207097271172991-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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