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Safety and efficacy of hydroxyapatite scaffold in the prevention of jaw osteonecrosis in vivo

dc.contributor.authorde Almeida, Adriana Duarte
dc.contributor.authorLeite, Fernanda Gomes
dc.contributor.authorChaud, Marco Vinícius
dc.contributor.authorRebelo, Márcia de Araújo
dc.contributor.authorBorges, Liliane Cristine Ferreira de Souza
dc.contributor.authorViroel, Fabia Judice Marques
dc.contributor.authorHataka, Alessandre [UNESP]
dc.contributor.authorGrotto, Denise
dc.contributor.institutionUniversity of Sorocaba (Uniso)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:14:38Z
dc.date.available2018-12-11T17:14:38Z
dc.date.issued2018-07-01
dc.description.abstractTwo scaffolds of chitosan/sodium alginate/hydroxyapatite (Ch/NaAlg/Hap) 1:1:0.2 and 1:1:0.6 were evaluated in the prevention of bisphosphonate-induced jaw osteonecrosis. Two groups of rats (n = 24, according to the euthanasia time: 15 or 30 days after the last Zoledronic acid (ZA) administration) were subdivided in four subgroups (n = 6): I – Control (saline + teeth extraction); II – ZA 0.6 mg/kg + teeth extraction; III – ZA + teeth extraction + scaffold 1:1:0.2; IV – ZA + teeth extraction + scaffold 1:1:0.6. Jaws were evaluated histologically and blood was evaluated for hematological and biochemical parameters. Histopathology showed significant osteonecrosis in AZ group. The scaffold's implantation, despite the inflammatory process, were able to prevent the osteonecrosis. In the 15-day euthanasia group, an increase in red blood cells and platelets was observed in the subgroup II. Hemoglobin and hematocrit decreased in subgroup IV compared to II. Hepatic transaminases and creatinine concentration increased significantly in subgroup II. Calcium concentration increased in subgroup IV compared to II. In the 30-day euthanasia group, no differences among the groups were observed for any parameter. Scaffolds proved to be efficient and safe to liver and kidney function. Some hematological parameters were altered by the scaffold, but returned to normal concentrations over time. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 1799–1808, 2018.en
dc.description.affiliationLaboratory of Toxicological Research University of Sorocaba (Uniso)
dc.description.affiliationLaboratory of Biomaterials and Nanotechnology University of Sorocaba (Uniso)
dc.description.affiliationDepartment of Veterinary Clinical Sciences School of Veterinary Medicine and Animal Science São Paulo State University (UNESP)
dc.description.affiliationUnespDepartment of Veterinary Clinical Sciences School of Veterinary Medicine and Animal Science São Paulo State University (UNESP)
dc.description.sponsorshipFinanciadora de Estudos e Projetos
dc.description.sponsorshipIdFinanciadora de Estudos e Projetos: FINEP-01.10.0659.00
dc.format.extent1799-1808
dc.identifierhttp://dx.doi.org/10.1002/jbm.b.33995
dc.identifier.citationJournal of Biomedical Materials Research - Part B Applied Biomaterials, v. 106, n. 5, p. 1799-1808, 2018.
dc.identifier.doi10.1002/jbm.b.33995
dc.identifier.issn1552-4981
dc.identifier.issn1552-4973
dc.identifier.scopus2-s2.0-85029348851
dc.identifier.urihttp://hdl.handle.net/11449/175161
dc.language.isoeng
dc.relation.ispartofJournal of Biomedical Materials Research - Part B Applied Biomaterials
dc.relation.ispartofsjr0,715
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectbone regeneration
dc.subjecthydroxyapatite
dc.subjectosteonecrosis
dc.subjectscaffold
dc.subjectzoledronic acid
dc.titleSafety and efficacy of hydroxyapatite scaffold in the prevention of jaw osteonecrosis in vivoen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.lattes5436331892008857[7]
unesp.author.orcid0000-0002-2023-212X[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina Veterinária e Zootecnia, Botucatupt
unesp.departmentClínica Veterinária - FMVZpt

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