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Functionalization of PCL-Based Fiber Scaffolds with Different Sources of Calcium and Phosphate and Odontogenic Potential on Human Dental Pulp Cells

dc.contributor.authorAnselmi, Caroline [UNESP]
dc.contributor.authorMendes Soares, Igor Paulino
dc.contributor.authorMota, Rafaella Lara Maia
dc.contributor.authorLeite, Maria Luísa
dc.contributor.authorRibeiro, Rafael Antonio de Oliveira
dc.contributor.authorFernandes, Lídia de Oliveira
dc.contributor.authorBottino, Marco C.
dc.contributor.authorde Souza Costa, Carlos Alberto
dc.contributor.authorHebling, Josimeri
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversity of Michigan
dc.contributor.institutionThe University of British Columbia (UBC)
dc.date.accessioned2025-04-29T20:03:37Z
dc.date.issued2024-04-01
dc.description.abstractThis study investigated the incorporation of sources of calcium, phosphate, or both into electrospun scaffolds and evaluated their bioactivity on human dental pulp cells (HDPCs). Additionally, scaffolds incorporated with calcium hydroxide (CH) were characterized for degradation, calcium release, and odontogenic differentiation by HDPCs. Polycaprolactone (PCL) was electrospun with or without 0.5% w/v of calcium hydroxide (PCL + CH), nano-hydroxyapatite (PCL + nHA), or β-glycerophosphate (PCL + βGP). SEM/EDS analysis confirmed fibrillar morphology and particle incorporation. HDPCs were cultured on the scaffolds to assess cell viability, adhesion, spreading, and mineralized matrix formation. PCL + CH was also evaluated for gene expression of odontogenic markers (RT-qPCR). Data were submitted to ANOVA and Student’s t-test (α = 5%). Added CH increased fiber diameter and interfibrillar spacing, whereas βGP decreased both. PCL + CH and PCL + nHA improved HDPC viability, adhesion, and proliferation. Mineralization was increased eightfold with PCL + CH. Scaffolds containing CH gradually degraded over six months, with calcium release within the first 140 days. CH incorporation upregulated DSPP and DMP1 expression after 7 and 14 days. In conclusion, CH- and nHA-laden PCL fiber scaffolds were cytocompatible and promoted HDPC adhesion, proliferation, and mineralized matrix deposition. PCL + CH scaffolds exhibit a slow degradation profile, providing sustained calcium release and stimulating HDPCs to upregulate odontogenesis marker genes.en
dc.description.affiliationDepartment of Morphology Orthodontics and Pediatric Dentistry School of Dentistry São Paulo State University (UNESP), SP
dc.description.affiliationDepartment of Cariology Restorative Sciences and Endodontics School of Dentistry University of Michigan
dc.description.affiliationDepartment of Dental Materials and Prosthodontics School of Dentistry São Paulo State University (UNESP), SP
dc.description.affiliationDepartment of Oral Health Sciences Faculty of Dentistry The University of British Columbia (UBC)
dc.description.affiliationDepartment of Restorative Dentistry School of Dentistry São Paulo State University (UNESP), SP
dc.description.affiliationDepartment of Physiology and Pathology School of Dentistry São Paulo State University (UNESP), SP
dc.description.affiliationUnespDepartment of Morphology Orthodontics and Pediatric Dentistry School of Dentistry São Paulo State University (UNESP), SP
dc.description.affiliationUnespDepartment of Dental Materials and Prosthodontics School of Dentistry São Paulo State University (UNESP), SP
dc.description.affiliationUnespDepartment of Restorative Dentistry School of Dentistry São Paulo State University (UNESP), SP
dc.description.affiliationUnespDepartment of Physiology and Pathology School of Dentistry São Paulo State University (UNESP), SP
dc.identifierhttp://dx.doi.org/10.3390/jfb15040097
dc.identifier.citationJournal of Functional Biomaterials, v. 15, n. 4, 2024.
dc.identifier.dimensionspub.1170632165
dc.identifier.doi10.3390/jfb15040097
dc.identifier.issn2079-4983
dc.identifier.lattes4517484241515548
dc.identifier.lattes8207097271172991
dc.identifier.orcid0000-0001-8100-3294
dc.identifier.orcid0000-0002-3189-1542
dc.identifier.orcid0000-0002-5748-5040
dc.identifier.orcid0000-0001-8740-2464
dc.identifier.orcid0000-0002-7455-6867
dc.identifier.orcid0000-0002-2846-2325
dc.identifier.pmcidPMC11051160
dc.identifier.pmid38667554
dc.identifier.scopus2-s2.0-85191548280
dc.identifier.urihttps://hdl.handle.net/11449/305597
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.subjectcalcium
dc.subjectcell-homing therapy
dc.subjectphosphates
dc.subjectpulp capping agents
dc.subjectscaffolds
dc.subjecttissue engineering
dc.titleFunctionalization of PCL-Based Fiber Scaffolds with Different Sources of Calcium and Phosphate and Odontogenic Potential on Human Dental Pulp Cellsen
dc.typeArtigopt
dspace.entity.typePublication
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unesp.author.orcid0000-0002-3189-1542[1]
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