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A new multiphase calcium phosphate graft material improves bone healing—An in vitro and in vivo analysis

dc.contributor.authorGuastaldi, Fernando Pozzi Semeghini [UNESP]
dc.contributor.authorMatheus, Henrique Rinaldi [UNESP]
dc.contributor.authorFaloni, Ana Paula de Souza
dc.contributor.authorde Almeida-Filho, Edson [UNESP]
dc.contributor.authorCominotte, Mariana Aline [UNESP]
dc.contributor.authorMoretti, Livia Alves Correa [UNESP]
dc.contributor.authorVerzola, Mario Henrique Arruda [UNESP]
dc.contributor.authorMarcantonio, Elcio [UNESP]
dc.contributor.authorde Almeida, Juliano Milanezi [UNESP]
dc.contributor.authorGuastaldi, Antonio Carlos [UNESP]
dc.contributor.authorCirelli, Joni Augusto [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionHarvard School of Dental Medicine
dc.contributor.institutionUniversity Center of Araraquara (UNIARA)
dc.date.accessioned2023-03-01T20:53:52Z
dc.date.available2023-03-01T20:53:52Z
dc.date.issued2022-01-01
dc.description.abstractThis study aims to evaluate the potential of a novel biomaterial synthesized from amorphous calcium phosphate (ACP), octacalcium phosphate (OCP), and hydroxyapatite (HA) to repair critical-sized defects (CSD) in rabbit calvaria. In vitro analyses of cell viability, cell proliferation, formation of mineral nodules, and cell differentiation using qPCR were performed for comparing experimental calcium phosphate (ECP), deproteinized bovine bone (DBB), and beta-tricalcium phosphate (β-TCP). Bilateral CSDs were created in 45 rabbit calvaria. Six groups were evaluated: ECP, ECP + fibrin sealant (ECP + S), coagulum, autogenous bone, DBB, and β-TCP. Euthanasia was performed at 2, 4, and 8 weeks, followed by micro-computed tomography and histological and immunohistochemical analyses. Results from in vitro analyses revealed similar biocompatibility for all tested materials and a tendency for higher gene expression of some bone markers in the ECP group than in β-TCP and DBB groups at 7 days. In contrast to that in DBB and β-TCP groups, ECP displayed growing bone volume over total volume percentage (BV/TV%) with time in vivo. Histological analysis revealed a greater number of giant cells and reduced size of grafted particles in ECP during all periods of analysis. RUNX-2 expression was statistically lower in ECP than DBB at 2 and 4 weeks. Despite no statistical significance, ECP presented the highest absolute values for ALP-expression at 2, 4, and 8 weeks compared with other groups. Together, our findings indicate that a combination of the ACP, OCP, and HA phases into ECP is beneficial and promising for bone regeneration.en
dc.description.affiliationDepartment of Diagnosis and Surgery São Paulo State University (Unesp) School of Dentistry, São Paulo
dc.description.affiliationDepartment of Oral and Maxillofacial Surgery Massachusetts General Hospital Harvard School of Dental Medicine
dc.description.affiliationDepartment of Health Sciences University Center of Araraquara (UNIARA), São Paulo
dc.description.affiliationDepartment of Physical Chemistry São Paulo State University (Unesp) Institute of Chemistry, São Paulo
dc.description.affiliationUnespDepartment of Diagnosis and Surgery São Paulo State University (Unesp) School of Dentistry, São Paulo
dc.description.affiliationUnespDepartment of Physical Chemistry São Paulo State University (Unesp) Institute of Chemistry, São Paulo
dc.identifierhttp://dx.doi.org/10.1002/jbm.b.35121
dc.identifier.citationJournal of Biomedical Materials Research - Part B Applied Biomaterials.
dc.identifier.doi10.1002/jbm.b.35121
dc.identifier.issn1552-4981
dc.identifier.issn1552-4973
dc.identifier.scopus2-s2.0-85133168915
dc.identifier.urihttp://hdl.handle.net/11449/241257
dc.language.isoeng
dc.relation.ispartofJournal of Biomedical Materials Research - Part B Applied Biomaterials
dc.sourceScopus
dc.subjectbiomaterials
dc.subjectbone regeneration
dc.subjectcalcium phosphates
dc.subjectrabbit calvarial defect
dc.titleA new multiphase calcium phosphate graft material improves bone healing—An in vitro and in vivo analysisen
dc.typeArtigo
unesp.author.orcid0000-0001-8554-8849[1]
unesp.author.orcid0000-0002-7082-9290[11]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Química, Araraquarapt
unesp.departmentFísico-Química - IQARpt

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