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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/15690
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dc.contributor.authorCosta, CAD-
dc.contributor.authorHebling, J.-
dc.contributor.authorGarcia-Godoy, F.-
dc.contributor.authorHanks, C. T.-
dc.date.accessioned2014-02-26T17:16:23Z-
dc.date.accessioned2014-05-20T13:44:43Z-
dc.date.accessioned2016-10-25T16:58:53Z-
dc.date.available2014-02-26T17:16:23Z-
dc.date.available2014-05-20T13:44:43Z-
dc.date.available2016-10-25T16:58:53Z-
dc.date.issued2003-09-01-
dc.identifierhttp://dx.doi.org/10.1016/S0142-9612(03)00253-9-
dc.identifier.citationBiomaterials. Oxford: Elsevier B.V., v. 24, n. 21, p. 3853-3858, 2003.-
dc.identifier.issn0142-9612-
dc.identifier.urihttp://hdl.handle.net/11449/15690-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/15690-
dc.description.abstractTo evaluate the cytotoxic effects of five glass-ionomer cements (GICs) on an odontoblast cell line (MDPC-23), disks of every material were prepared and divided into Group 1: Vitrebond, Group 2: Vitremer, Group 3: Fuji IILC, Group 4: Fuji IX GP, Group 5: Ketac-Molar, Group 6: Z-100 (positive control). In Group 7, phosphate-buffered saline solution (negative control) was applied on filter paper. After placing the samples in the bottom of wells, the cells (30,000 cells/cm(2)) were plated and incubated for 72 h. The cell number was counted, the cell morphology was assessed by scanning electron microscopy and the cell metabolism was evaluated using methyltetrazolium assay. The statistical analysis of Kruskal-Wallis was used to determine if the scores obtained for the cell metabolism and number of cells were different at the 95% confidence level. In groups 1, 2, 3, 4, 5, and 6 the materials decreased the cell number by 74.5% 75.5%, 45.5%, 29.5%, 32.5%, and 88.5%, respectively. In groups 1, 2, 3, 4, and 5, the experimental GICs reduced the cell metabolism by 79%, 84%, 54%, 40%, and 42.5%, respectively. Despite the fact that all experimental materials were cytotoxic to the MDPC-23 cells, the GICs were the least cytotoxic. on the other hand, the RMGICs caused the highest cytophatic effects. (C) 2003 Elsevier B.V. Ltd. All rights reserved.en
dc.format.extent3853-3858-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectcytotoxicitypt
dc.subjectglass-ionomer cementpt
dc.subjectculturept
dc.subjectodontoblastpt
dc.titleIn vitro cytotoxicity of five glass-ionomer cementsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionNova SE Univ-
dc.contributor.institutionUniversity of Michigan-
dc.description.affiliationUniv São Paulo State, UNESP, Sch Dent, Dept Physiol & Pathol, BR-14801903 Araraquara, SP, Brazil-
dc.description.affiliationUniv São Paulo State, UNESP, Sch Dent, Dept Orthodont & Pediat Dent, BR-14801903 Araraquara, SP, Brazil-
dc.description.affiliationNova SE Univ, Coll Dent Med, Dept Restorat Dent, Ft Lauderdale, FL 33328 USA-
dc.description.affiliationNova SE Univ, Coll Dent Med, Dept Pediat Dent, Ft Lauderdale, FL 33328 USA-
dc.description.affiliationUniv Michigan, Sch Dent, Dept Oral Med Pathol & Oncol, Ann Arbor, MI 48109 USA-
dc.description.affiliationUnespUniv São Paulo State, UNESP, Sch Dent, Dept Physiol & Pathol, BR-14801903 Araraquara, SP, Brazil-
dc.description.affiliationUnespUniv São Paulo State, UNESP, Sch Dent, Dept Orthodont & Pediat Dent, BR-14801903 Araraquara, SP, Brazil-
dc.identifier.doi10.1016/S0142-9612(03)00253-9-
dc.identifier.wosWOS:000183992700024-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofBiomaterials-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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