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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/15107
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dc.contributor.authorNagata, Maria José Hitomi-
dc.contributor.authorFurlaneto, Flavia A. C.-
dc.contributor.authorMoretti, Antonio J.-
dc.contributor.authorBouquot, Jerry E.-
dc.contributor.authorAhn, Chul W.-
dc.contributor.authorMessora, Michel R.-
dc.contributor.authorFucini, Stephen E.-
dc.contributor.authorGarcia, Valdir Gouveia-
dc.contributor.authorBosco, Álvaro Francisco-
dc.date.accessioned2013-09-30T18:29:35Z-
dc.date.accessioned2014-05-20T13:43:20Z-
dc.date.accessioned2016-10-25T16:57:57Z-
dc.date.available2013-09-30T18:29:35Z-
dc.date.available2014-05-20T13:43:20Z-
dc.date.available2016-10-25T16:57:57Z-
dc.date.issued2010-11-01-
dc.identifierhttp://dx.doi.org/10.1002/jbm.b.31710-
dc.identifier.citationJournal of Biomedical Materials Research Part B-applied Biomaterials. Hoboken: Wiley-liss, v. 95B, n. 2, p. 269-275, 2010.-
dc.identifier.issn1552-4973-
dc.identifier.urihttp://hdl.handle.net/11449/15107-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/15107-
dc.description.abstractThis study analyzed histologically the influence of new spherical bioactive glass (NBG) particles with or without a calcium sulfate (CS) barrier on bone healing in surgically created critical-size defects (CSD) in rat calvaria. A CSD was made in each calvarium of 60 rats, which were divided into three groups: C (control): the defect was filled with blood clot only; NBG: the defect was filled with NBG only; and NBG/CS: the defect was filled with NBG covered by CS barrier. Subgroups were euthanized at 4 or 12 weeks. Amounts of new bone and remnants of implanted materials were calculated as percentages of total area of the original defect. Data were statistically analyzed. In contrast to Group C, thickness throughout defects in Groups NBG and NBG/CS was similar to the original calvarium. At 4 weeks, Group C had significantly more bone formation than Group NBG/CS. No significant differences were found between Group NBG and either Group C or Group NBG/CS. At 12 weeks, Group C had significantly more bone formation than Group NBG or NBG/CS. NBG particles, used with or without a CS barrier, maintained volume and contour of area grafted in CSD. Presence of remaining NBG particles might have accounted for smaller amount of new bone in Groups NBG and NBG/CS at 12 weeks postoperative. (C) 2010 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 95B: 269-275, 2010.en
dc.description.sponsorshipFundação para o Desenvolvimento da UNESP (FUNDUNESP)-
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.format.extent269-275-
dc.language.isoeng-
dc.publisherWiley-liss-
dc.sourceWeb of Science-
dc.subjectbone regenerationen
dc.subjectbone substitutesen
dc.subjectbioactive glass 45S5en
dc.subjectcalcium sulfateen
dc.titleBone healing in critical-size defects treated with new bioactive glass/calcium sulfate: A histologic and histometric study in rat calvariaen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniv N Carolina-
dc.contributor.institutionUniv Texas Hlth Sci Ctr Dent Branch-
dc.contributor.institutionUniv Texas SW Med Ctr Dallas-
dc.description.affiliationSão Paulo State Univ UNESP, Dent Sch Aracatuba, Div Periodont, Dept Surg, São Paulo, Brazil-
dc.description.affiliationSão Paulo State Univ UNESP, Dent Sch Aracatuba, Integrated Clin, São Paulo, Brazil-
dc.description.affiliationUniv N Carolina, Dept Periodont, Chapel Hill, NC USA-
dc.description.affiliationUniv Texas Hlth Sci Ctr Dent Branch, Dept Diagnost Sci, Houston, TX USA-
dc.description.affiliationUniv Texas SW Med Ctr Dallas, Dept Clin Sci, Dallas, TX 75390 USA-
dc.description.affiliationUnespSão Paulo State Univ UNESP, Dent Sch Aracatuba, Div Periodont, Dept Surg, São Paulo, Brazil-
dc.description.affiliationUnespSão Paulo State Univ UNESP, Dent Sch Aracatuba, Integrated Clin, São Paulo, Brazil-
dc.description.sponsorshipIdFUNDUNESP: 00933/07-DFP-
dc.description.sponsorshipIdCAPES: 1090/06-2-
dc.identifier.doi10.1002/jbm.b.31710-
dc.identifier.wosWOS:000283103400004-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Biomedical Materials Research Part B: Applied Biomaterials-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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