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Bone healing in critical-size defects treated with new bioactive glass/calcium sulfate: A histologic and histometric study in rat calvaria

dc.contributor.authorNagata, Maria José Hitomi [UNESP]
dc.contributor.authorFurlaneto, Flavia A. C. [UNESP]
dc.contributor.authorMoretti, Antonio J.
dc.contributor.authorBouquot, Jerry E.
dc.contributor.authorAhn, Chul W.
dc.contributor.authorMessora, Michel R. [UNESP]
dc.contributor.authorFucini, Stephen E. [UNESP]
dc.contributor.authorGarcia, Valdir Gouveia [UNESP]
dc.contributor.authorBosco, Álvaro Francisco [UNESP]
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.date.accessioned2013-09-30T18:29:35Z
dc.date.accessioned2014-05-20T13:43:20Z
dc.date.available2013-09-30T18:29:35Z
dc.date.available2014-05-20T13:43:20Z
dc.date.issued2010-11-01
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.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.sponsorshipFundação para o Desenvolvimento da UNESP (FUNDUNESP)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipIdFUNDUNESP: 00933/07-DFP
dc.description.sponsorshipIdCAPES: 1090/06-2
dc.format.extent269-275
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.doi10.1002/jbm.b.31710
dc.identifier.issn1552-4973
dc.identifier.lattes8399870097572073
dc.identifier.lattes4068921369233125
dc.identifier.lattes9831236034935598
dc.identifier.urihttp://hdl.handle.net/11449/15107
dc.identifier.wosWOS:000283103400004
dc.language.isoeng
dc.publisherWiley-liss
dc.relation.ispartofJournal of Biomedical Materials Research Part B: Applied Biomaterials
dc.relation.ispartofjcr3.373
dc.relation.ispartofsjr0,715
dc.rights.accessRightsAcesso restritopt
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.typeArtigopt
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dcterms.rightsHolderWiley-liss
dspace.entity.typePublication
relation.isOrgUnitOfPublication8b3335a4-1163-438a-a0e2-921a46e0380d
relation.isOrgUnitOfPublication.latestForDiscovery8b3335a4-1163-438a-a0e2-921a46e0380d
unesp.author.lattes8399870097572073
unesp.author.lattes4068921369233125
unesp.author.lattes9831236034935598
unesp.author.orcid0000-0002-8072-3983[2]
unesp.author.orcid0000-0001-5903-5652[1]
unesp.author.orcid0000-0001-8485-9645[6]
unesp.author.orcid0000-0002-6715-8334[8]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatubapt
unesp.departmentCirurgia e Clínica Integrada - FOApt

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