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Cytotoxicity and Biomineralization Potential of Flavonoids Incorporated into PNVCL Hydrogels

dc.contributor.authorBraga, Gabriela Pacheco de Almeida [UNESP]
dc.contributor.authorCaiaffa, Karina Sampaio [UNESP]
dc.contributor.authorRabelo, Rafaela Laruzo [UNESP]
dc.contributor.authorSantos, Vanessa Rodrigues dos [UNESP]
dc.contributor.authorSouza, Amanda Caselato Andolfatto [UNESP]
dc.contributor.authorRibeiro, Lucas da Silva
dc.contributor.authorCamargo, Emerson Rodrigues de
dc.contributor.authorPrakki, Anuradha
dc.contributor.authorDuque, Cristiane [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.contributor.institutionUniversity of Toronto
dc.date.accessioned2023-07-29T13:48:15Z
dc.date.available2023-07-29T13:48:15Z
dc.date.issued2023-03-01
dc.description.abstractThis study aimed to evaluate the effects of flavonoids incorporated into poly(N-vinylcaprolactam) (PNVCL) hydrogel on cell viability and mineralization markers of odontoblast-like cells. MDPC-23 cells were exposed to ampelopsin (AMP), isoquercitrin (ISO), rutin (RUT) and control calcium hydroxide (CH) for evaluation of cell viability, total protein (TP) production, alkaline phosphatase (ALP) activity and mineralized nodule deposition by colorimetric assays. Based on an initial screening, AMP and CH were loaded into PNVCL hydrogels and had their cytotoxicity and effect on mineralization markers determined. Cell viability was above 70% when MDPC-23 cells were treated with AMP, ISO and RUT. AMP showed the highest ALP activity and mineralized nodule deposition. Extracts of PNVCL+AMP and PNVCL+CH in culture medium (at the dilutions of 1/16 and 1/32) did not affect cell viability and stimulated ALP activity and mineralized nodules’ deposition, which were statistically higher than the control in osteogenic medium. In conclusion, AMP and AMP-loaded PNVCL hydrogels were cytocompatible and able to induce bio-mineralization markers in odontoblast-cells.en
dc.description.affiliationDepartment of Preventive and Restorative Dentistry Araçatuba Dental School São Paulo State University (UNESP), SP
dc.description.affiliationDepartment of Chemistry Federal University of São Carlos (UFSCar), SP
dc.description.affiliationDental Research Institute Faculty of Dentistry University of Toronto
dc.description.affiliationUnespDepartment of Preventive and Restorative Dentistry Araçatuba Dental School São Paulo State University (UNESP), SP
dc.identifierhttp://dx.doi.org/10.3390/jfb14030139
dc.identifier.citationJournal of Functional Biomaterials, v. 14, n. 3, 2023.
dc.identifier.dimensionspub.1155909735
dc.identifier.doi10.3390/jfb14030139
dc.identifier.issn2079-4983
dc.identifier.orcid0000-0003-2893-5353
dc.identifier.orcid0000-0002-8969-9043
dc.identifier.orcid0000-0002-2575-279X
dc.identifier.orcid0000-0001-8725-2136
dc.identifier.orcid0000-0003-1104-9283
dc.identifier.pmcidPMC10058549
dc.identifier.pmid36976063
dc.identifier.scopus2-s2.0-85151120660
dc.identifier.urihttp://hdl.handle.net/11449/248591
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofJournal of Functional Biomaterials
dc.rights.accessRightsAcesso abertopt
dc.rights.sourceRightsoa_all
dc.rights.sourceRightsgold
dc.sourceScopus
dc.sourceDimensions
dc.subjectalkaline phosphatase
dc.subjectcytotoxicity
dc.subjectdentin mineralization
dc.subjectflavonoids
dc.subjecthydrogel
dc.subjectodontoblasts
dc.titleCytotoxicity and Biomineralization Potential of Flavonoids Incorporated into PNVCL Hydrogelsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication8b3335a4-1163-438a-a0e2-921a46e0380d
relation.isOrgUnitOfPublication.latestForDiscovery8b3335a4-1163-438a-a0e2-921a46e0380d
unesp.author.orcid0000-0001-8725-2136[4]
unesp.author.orcid0000-0002-8969-9043[8]
unesp.author.orcid0000-0002-2575-279X[9]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatubapt
unesp.departmentOdontologia Restauradora - FOApt

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