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Injectable β-TCP/MCPM cement associated with mesoporous silica for bone regeneration: Characterization and toxicity evaluation

dc.contributor.authorMendes, L. S. [UNESP]
dc.contributor.authorSaska, S. [UNESP]
dc.contributor.authorCoelho, F. [UNESP]
dc.contributor.authorCapote, T S De O [UNESP]
dc.contributor.authorScarel-Caminaga, R. M. [UNESP]
dc.contributor.authorMarchetto, R. [UNESP]
dc.contributor.authorCarrodeguas, R. G.
dc.contributor.authorGaspar, A. M.M. [UNESP]
dc.contributor.authorRodríguez, M. A.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionAzurebio S.L.
dc.contributor.institutionCSIC
dc.date.accessioned2018-12-11T16:52:09Z
dc.date.available2018-12-11T16:52:09Z
dc.date.issued2018-02-08
dc.description.abstractCalcium phosphate cement has been widely investigated as a bone graft substitute due to its excellent self-setting ability, biocompatibility, osteoconductivity and moldability. In addition, mesoporous materials have been studied as potential materials for application in medical devices due to their large surface area, which is capable of loading numerous biological molecules, besides being bioactive. In this study, bone β-TCP-MCPM-based injectable cement with mesoporous silica particles was synthesized and characterized in terms of its mechanical properties, microstructure, porosity, injectability, in vitro bioactivity and degradability; together with toxicity effects in CHO-K1 cell culture. The results showed that the β-TCP-MCPM cement is bioactive after soaking in simulated body fluid solution, and mesoporous silica particles provided better physicochemical properties compared with silica-free cement. Toxicity assays showed low CHO-K1 cell viability after treatment with more concentrated extracts (200 mg ml-1). However, this behavior did not compromise the reproductive capacity and did not promote significant DNA damage in those cells. In conclusion, the β-TCP-MCPM cement associated with mesoporous silica might be considered as a potential bone substitute for the repair and regeneration of bone defects.en
dc.description.affiliationSão Paulo State University (Unesp) Institute of Chemistry
dc.description.affiliationSão Paulo State University (Unesp) School of Dentistry
dc.description.affiliationAzurebio S.L.
dc.description.affiliationInstituto de Cerámica y Vidrio CSIC
dc.description.affiliationUnespSão Paulo State University (Unesp) Institute of Chemistry
dc.description.affiliationUnespSão Paulo State University (Unesp) School of Dentistry
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2012/21735-6
dc.identifierhttp://dx.doi.org/10.1088/1748-605X/aa9085
dc.identifier.citationBiomedical Materials (Bristol), v. 13, n. 2, 2018.
dc.identifier.doi10.1088/1748-605X/aa9085
dc.identifier.file2-s2.0-85042662748.pdf
dc.identifier.issn1748-605X
dc.identifier.issn1748-6041
dc.identifier.scopus2-s2.0-85042662748
dc.identifier.urihttp://hdl.handle.net/11449/170722
dc.language.isoeng
dc.relation.ispartofBiomedical Materials (Bristol)
dc.relation.ispartofsjr0,768
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectbioactivity
dc.subjectbone repair
dc.subjectcalcium phosphate cement
dc.subjectinjectability
dc.subjectmesoporous silica
dc.subjecttoxicity analysis
dc.titleInjectable β-TCP/MCPM cement associated with mesoporous silica for bone regeneration: Characterization and toxicity evaluationen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.lattes8379925533335630[8]
unesp.author.orcid0000-0001-5468-4397[1]
unesp.author.orcid0000-0002-7168-9971[8]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt

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