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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/15973
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dc.contributor.authorSalles, Loise Pedrosa-
dc.contributor.authorGomes-Cornelio, Ana Livia-
dc.contributor.authorGuimaraes, Felipe Coutinho-
dc.contributor.authorHerrera, Bruno Schneider-
dc.contributor.authorBao, Sonia Nair-
dc.contributor.authorRossa-Junior, Carlos-
dc.contributor.authorGuerreiro-Tanomaru, Juliane Maria-
dc.contributor.authorTanomaru-Filho, Mario-
dc.date.accessioned2013-09-30T18:31:50Z-
dc.date.accessioned2014-05-20T13:45:25Z-
dc.date.accessioned2016-10-25T16:59:26Z-
dc.date.available2013-09-30T18:31:50Z-
dc.date.available2014-05-20T13:45:25Z-
dc.date.available2016-10-25T16:59:26Z-
dc.date.issued2012-07-01-
dc.identifierhttp://dx.doi.org/10.1016/j.joen.2012.02.018-
dc.identifier.citationJournal of Endodontics. New York: Elsevier B.V., v. 38, n. 7, p. 971-976, 2012.-
dc.identifier.issn0099-2399-
dc.identifier.urihttp://hdl.handle.net/11449/15973-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/15973-
dc.description.abstractIntroduction: The main purpose of this study was to evaluate the biocompatibility and bioactivity of a new mineral trioxide aggregate (MTA)-based endodontic sealer, MTA Fillapex (MTA-F; Angelus, Londrina, Brazil), in human cell culture. Methods: Human osteoblast-like cells (Saos-2) were exposed for 1, 2, 3, and 7 days to MTA-F, Epiphany SE (EP-SE; SybronEndo, Orange, CA), and zinc oxide-eugenol sealer (ZOE). Unexposed cultures were the control group (CT). The viability of the cells was assessed by MTT assay and the morphology by scanning electron microscopy (SEM). The bioactivity of MTA-F was evaluated by alkaline phosphatase activity (ALP) and the detection of calcium deposits in the culture with alizarin red stain (ARS). Energy-dispersive X-ray spectroscopy (EDS) was used to chemically characterize the hydroxyapatite crystallites (HAP). Saos-2 cells were cultured for 21 days for ARS and SEM/EDS. ARS results were expressed as the number of stained nodules per area. Statistical analysis was performed with analysis of variance and Bonferroni tests (P < .01). Results: MTA-F exposure for 1, 2, and 3 days resulted in increased cytotoxicity. In contrast, viability increased after 7 days of exposure to MTA-F. Exposure to EP-SE and ZOE was cytotoxic at all time points. At day 7, ALP activity increase was significant in the MTA-F group. MTA-F presented the highest percentage of ARS-stained nodules (MTA-F > CT > EP-SE > ZOE). SEM/EDS analysis showed hydroxyapatite crystals only in the MTA-F and CT groups. In the MTA-F group, crystallite morphology and chemical composition were different from CT. Conclusions: After setting, the cytotoxicity of MTA-F decreases and the sealer present; suitable bioactivity to stimulate HAP crystal nucleation. (J Endod 2012;38:971-976)en
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.description.sponsorshipFundação de Apoio à Pesquisa do Distrito Federal (FAPDF)-
dc.description.sponsorshipFinanciadora de Estudos e Projetos (FINEP)-
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.format.extent971-976-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectBioactivityen
dc.subjectbiocompatibilityen
dc.subjecthydroxyapatiteen
dc.subjectmineral trioxide aggregate sealeren
dc.titleMineral Trioxide Aggregate-based Endodontic Sealer Stimulates Hydroxyapatite Nucleation in Human Osteoblast-like Cell Cultureen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de Brasília (UnB)-
dc.description.affiliationSão Paulo State Univ, Sch Dent, Dept Restorat Dent, São Paulo, Brazil-
dc.description.affiliationUniversidade de Brasilia (UnB), Inst Biol Sci, Dept Cellular Biol, BR-70910900 Brasilia, DF, Brazil-
dc.description.affiliationSão Paulo State Univ, Araraquara Dent Sch, Dept Diag & Surg, São Paulo, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Sch Dent, Dept Restorat Dent, São Paulo, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Araraquara Dent Sch, Dept Diag & Surg, São Paulo, Brazil-
dc.description.sponsorshipIdFAPESP: 10/10769-1-
dc.identifier.doi10.1016/j.joen.2012.02.018-
dc.identifier.wosWOS:000305850400018-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Endodontics-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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