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dc.contributor.authorRaposo-Amaral, Cassio Eduardo-
dc.contributor.authorBueno, Daniela Franco-
dc.contributor.authorAlmeida, Ana Beatriz-
dc.contributor.authorJorgetti, Vanda-
dc.contributor.authorCosta, Cristiane Cabral-
dc.contributor.authorGouveia, Cecília Helena-
dc.contributor.authorVulcano, Luiz Carlos-
dc.contributor.authorFanganiello, Roberto D.-
dc.contributor.authorPassos-Bueno, Maria Rita-
dc.contributor.authorAlonso, Nivaldo-
dc.date.accessioned2015-12-07T15:31:01Z-
dc.date.accessioned2016-10-25T21:22:34Z-
dc.date.available2015-12-07T15:31:01Z-
dc.date.available2016-10-25T21:22:34Z-
dc.date.issued2014-
dc.identifierhttp://dx.doi.org/10.1177/2041731413519352-
dc.identifier.citationJournal Of Tissue Engineering, v. 5, p. 1-11, 2014.-
dc.identifier.issn2041-7314-
dc.identifier.urihttp://hdl.handle.net/11449/131031-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/131031-
dc.description.abstractNew strategies to fulfill craniofacial bone defects have gained attention in recent years due to the morbidity of autologous bone graft harvesting. We aimed to evaluate the in vivo efficacy of bone tissue engineering strategy using mesenchymal stem cells associated with two matrices (bovine bone mineral and α-tricalcium phosphate), compared to an autologous bone transfer. A total of 28 adult, male, non-immunosuppressed Wistar rats underwent a critical-sized osseous defect of 5 mm diameter in the alveolar region. Animals were divided into five groups. Group 1 (n = 7) defects were repaired with autogenous bone grafts; Group 2 (n = 5) defects were repaired with bovine bone mineral free of cells; Group 3 (n = 5) defects were repaired with bovine bone mineral loaded with mesenchymal stem cells; Group 4 (n = 5) defects were repaired with α-tricalcium phosphate free of cells; and Group 5 (n = 6) defects were repaired with α-tricalcium phosphate loaded with mesenchymal stem cells. Groups 2-5 were compared to Group 1, the reference group. Healing response was evaluated by histomorphometry and computerized tomography. Histomorphometrically, Group 1 showed 60.27% ± 16.13% of bone in the defect. Groups 2 and 3 showed 23.02% ± 8.6% (p = 0.01) and 38.35% ± 19.59% (p = 0.06) of bone in the defect, respectively. Groups 4 and 5 showed 51.48% ± 11.7% (p = 0.30) and 61.80% ± 2.14% (p = 0.88) of bone in the defect, respectively. Animals whose bone defects were repaired with α-tricalcium phosphate and mesenchymal stem cells presented the highest bone volume filling the defects; both were not statistically different from autogenous bone.en
dc.format.extent1-11-
dc.language.isoeng-
dc.sourcePubMed-
dc.subjectStem cellen
dc.subjectAlveolar defecten
dc.subjectBiomaterialen
dc.subjectBoneen
dc.subjectBone tissue engineeringen
dc.subjectOsseous defecten
dc.subjectΑ-tricalcium phosphateen
dc.titleIs bone transplantation the gold standard for repair of alveolar bone defects?en
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartamento de Cirurgia Plástica e Queimaduras, Faculdade de Medicina, Universidade de São Paulo (USP), São Paulo, Brazil.-
dc.description.affiliationCentro de Estudos do Genoma Humano, Instituto de Biociências, Universidade de São Paulo (USP), São Paulo, Brazil.-
dc.description.affiliationDepartamento de Clínica Médica, Faculdade de Medicina, Universidade de São Paulo (USP), São Paulo, Brazil.-
dc.description.affiliationFaculdade de Medicina Veterinária e Zootecnia, Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP), São Paulo, Brazil.-
dc.description.affiliationUnespFaculdade de Medicina Veterinária e Zootecnia, Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP), São Paulo, Brazil.-
dc.identifier.doi10.1177/2041731413519352-
dc.rights.accessRightsAcesso aberto-
dc.identifier.filePMC3924878.pdf-
dc.relation.ispartofJournal Of Tissue Engineering-
dc.identifier.pubmed24551445-
dc.identifier.pmcPMC3924878-
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