Characterization and cytotoxicity evaluation of bio-inspired bioactive Glass/Collagen/Magnesium composites

dc.contributor.authorGABBAI-ARMELIN, P.R.pt_BR
dc.contributor.authorFERNANDES, K.R.pt_BR
dc.contributor.authorMAGRI, A.M.P.pt_BR
dc.contributor.authorSILVA, A.C. dapt_BR
dc.contributor.authorFORTULAN, C.A.pt_BR
dc.contributor.authorRENNO, A.C.M.pt_BR
dc.coverageInternacionalpt_BR
dc.date.accessioned2019-08-09T12:45:31Z
dc.date.available2019-08-09T12:45:31Z
dc.date.issued2019pt_BR
dc.description.abstractBone fractures are a common clinical event related to trauma, aging or diseases. Since bone repair is complex, abnormal consolidation may occur or, even, non-union. Biomaterials have a key role in this context, since they can stimulate bone cell differentiation, accelerating the healing process. Bioactive glasses (BG) represent a promising class of biomaterials due to its high bioactivity and osteogenic potential. Nevertheless, the osteoconductive properties of BG may not be enough to stimulate consolidation in critical situations. Thus, it was hypothesized that enriching BG with other materials such as collagen (Col) and magnesium (Mg), trying to make a composite with similar properties to bone tissue, would constitute a more suitable graft for tissue engineering. This work aimed at obtaining BG/Col/Mg composites and evaluating their physicochemical features. Moreover, L929 and MC3T3-E1 cell culture studies were done to investigate the cytotoxicity of the composites. The results showed that Mg could be successfully introduced, at different percentages (1, 3 and 5%), into BG and BG/Col composites, improving mechanical properties and retaining the bioactivity of BG. Ca assay measurements demonstrated that reactions in the Mg/solution interface, i.e. reactions between Mg and the ions in the simulated body fluid (SBF) have led to an increased Ca uptake for compositescontaining 3 and 5% Mg compared to plain BG and BG/Col. In vitro studies showed that BG and BG/Col containing 1% of Mg were non-cytotoxic and biocompatible. This percentage of Mg is promising for forward works. Our data on the present BG/Mg and BG/Col/Mg-based composites are encouraging and may lead to further molecular and cell culture studies, and in vivo investigations to clarify the biological performance of these new biomaterials.pt_BR
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)pt_BR
dc.description.sponsorshipIDFAPESP: 15/20704-8pt_BR
dc.format.extent201-209pt_BR
dc.identifier.citationGABBAI-ARMELIN, P.R.; FERNANDES, K.R.; MAGRI, A.M.P.; SILVA, A.C. da; FORTULAN, C.A.; RENNO, A.C.M. Characterization and cytotoxicity evaluation of bio-inspired bioactive Glass/Collagen/Magnesium composites. <b>Materials Chemistry and Physics</b>, v. 228, p. 201-209, 2019. DOI: <a href="https://dx.doi.org/10.1016/j.matchemphys.2019.02.072">10.1016/j.matchemphys.2019.02.072</a>. Disponível em: http://repositorio.ipen.br/handle/123456789/30060.
dc.identifier.doi10.1016/j.matchemphys.2019.02.072pt_BR
dc.identifier.issn0254-0584pt_BR
dc.identifier.percentilfi63.535pt_BR
dc.identifier.percentilfiCiteScore75.00
dc.identifier.urihttp://repositorio.ipen.br/handle/123456789/30060
dc.identifier.vol228pt_BR
dc.relation.ispartofMaterials Chemistry and Physicspt_BR
dc.rightsopenAccesspt_BR
dc.subjectskeleton
dc.subjecttoxicity
dc.subjectcollagen
dc.subjectmagnesium
dc.subjectglass
dc.subjectcomposite materials
dc.subjectskeletal diseases
dc.subjectbiological repair
dc.subjectbiological materials
dc.titleCharacterization and cytotoxicity evaluation of bio-inspired bioactive Glass/Collagen/Magnesium compositespt_BR
dc.typeArtigo de periódicopt_BR
dspace.entity.typePublication
ipen.autorANTONIO CARLOS DA SILVA
ipen.codigoautor2949
ipen.contributor.ipenauthorANTONIO CARLOS DA SILVA
ipen.date.recebimento19-08
ipen.identifier.fi3.408pt_BR
ipen.identifier.fiCiteScore4.9
ipen.identifier.ipendoc25854pt_BR
ipen.identifier.iwosWoSpt_BR
ipen.range.fi3.000 - 4.499
ipen.range.percentilfi50.00 - 74.99
ipen.type.genreArtigo
relation.isAuthorOfPublication839a3a2d-55ca-4376-993c-a8279c5cf017
relation.isAuthorOfPublication.latestForDiscovery839a3a2d-55ca-4376-993c-a8279c5cf017
sigepi.autor.atividadeSILVA, A.C. da:2949:720:N

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