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Glucose is an active chemical agent on degradation of hydroxyapatite nanostructure

dc.contributor.authorMartins, Murillo L.
dc.contributor.authorIessi, Isabela L.
dc.contributor.authorQuintino, Michelle P.
dc.contributor.authorDamasceno, Débora C. [UNESP]
dc.contributor.authorRodrigues, Cloves G.
dc.contributor.institutionPontifical Catholic University of Goias
dc.contributor.institutionPaul Langerhans Institute Dresden of the Helmholtz Zentrum München at the University Hospital and Faculty of Medicine Carl Gustav Carus of TU Dresden
dc.contributor.institutionPontifical Catholic University of Goiás
dc.contributor.institutionState University of Goiás (UEG)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2020-12-12T01:39:25Z
dc.date.available2020-12-12T01:39:25Z
dc.date.issued2020-01-15
dc.description.abstractThe mechanisms governing the glucose/bone mineral interface are still not fully described. By recognizing the multidisciplinary character of this problem, in this work we exclude any biological variable and provide insight with a pure materials science perspective. For that, hydroxyapatite nanoparticles were prepared in media with glucose concentrations analogous to those found in healthy and diabetic patients. We report that the influence of glucose over the nanoparticles depends on the stage in which it is added to the synthesis. First, nanoparticles precipitated in glucose-rich solutions present, as expected, decrease in crystallinity. However, this effect is driven by the action of glucose as an active chemical agent, rather than simply as a dispersant. This effect becomes more severe when hydroxyapatite nanoparticles are separately prepared and further allowed to interact with glucose. In this scenario, the deterioration of the nanoparticles’ bulk structure accompanies increase in surface crystallinity. In general, the effects of glucose over hydroxyapatite are concentration-dependent and associated with the precipitation of secondary phases - calcium hydroxide and calcium carbonate. Finally, we present illustrative data from bone minerals from one diabetic and one healthy rat and show that our methods and outcomes are employable in future biomedical investigations.en
dc.description.affiliationPost-Graduation Program in Industrial and Systems Engineering Pontifical Catholic University of Goias
dc.description.affiliationPaul Langerhans Institute Dresden of the Helmholtz Zentrum München at the University Hospital and Faculty of Medicine Carl Gustav Carus of TU Dresden
dc.description.affiliationSchool of Exact Sciences and Computing Pontifical Catholic University of Goiás
dc.description.affiliationState University of Goiás (UEG)
dc.description.affiliationLaboratory of Experimental Research on Gynecology and Obstetrics Botucatu Medical School Sao Paulo State University (UNESP)
dc.description.affiliationUnespLaboratory of Experimental Research on Gynecology and Obstetrics Botucatu Medical School Sao Paulo State University (UNESP)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de Goiás
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdFundação de Amparo à Pesquisa do Estado de Goiás: 20171026700070
dc.description.sponsorshipIdCNPq: 205609/2014-7
dc.description.sponsorshipIdCNPq: 300509/2017-0
dc.identifierhttp://dx.doi.org/10.1016/j.matchemphys.2019.122166
dc.identifier.citationMaterials Chemistry and Physics, v. 240.
dc.identifier.doi10.1016/j.matchemphys.2019.122166
dc.identifier.issn0254-0584
dc.identifier.scopus2-s2.0-85072178683
dc.identifier.urihttp://hdl.handle.net/11449/199424
dc.language.isoeng
dc.relation.ispartofMaterials Chemistry and Physics
dc.sourceScopus
dc.subjectGlucose
dc.subjectHydroxyapatite
dc.subjectInfrared spectroscopy
dc.subjectX-ray diffraction
dc.titleGlucose is an active chemical agent on degradation of hydroxyapatite nanostructureen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicationec2d1b26-b2b3-4b5f-b820-763909960fff
relation.isDepartmentOfPublication.latestForDiscoveryec2d1b26-b2b3-4b5f-b820-763909960fff
relation.isOrgUnitOfPublicationa3cdb24b-db92-40d9-b3af-2eacecf9f2ba
relation.isOrgUnitOfPublication.latestForDiscoverya3cdb24b-db92-40d9-b3af-2eacecf9f2ba
unesp.author.orcid0000-0002-3883-9114[1]
unesp.author.orcid0000-0003-0140-9847 0000-0003-0140-9847[5]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentGinecologia e Obstetrícia - FMBpt

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