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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

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Autor(a) principal: Anselmi, Caroline [UNESP]
Data de Publicação: 2024
Outros Autores: Mendes Soares, Igor Paulino [UNESP], Mota, Rafaella Lara Maia [UNESP], Leite, Maria Luísa, Ribeiro, Rafael Antonio de Oliveira [UNESP], Fernandes, Lídia de Oliveira [UNESP], Bottino, Marco C., de Souza Costa, Carlos Alberto [UNESP], Hebling, Josimeri [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3390/jfb15040097
https://hdl.handle.net/11449/305597
Resumo: This 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.
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spelling Functionalization of PCL-Based Fiber Scaffolds with Different Sources of Calcium and Phosphate and Odontogenic Potential on Human Dental Pulp Cellscalciumcell-homing therapyphosphatespulp capping agentsscaffoldstissue engineeringThis 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.Department of Morphology Orthodontics and Pediatric Dentistry School of Dentistry São Paulo State University (UNESP), SPDepartment of Cariology Restorative Sciences and Endodontics School of Dentistry University of MichiganDepartment of Dental Materials and Prosthodontics School of Dentistry São Paulo State University (UNESP), SPDepartment of Oral Health Sciences Faculty of Dentistry The University of British Columbia (UBC)Department of Restorative Dentistry School of Dentistry São Paulo State University (UNESP), SPDepartment of Physiology and Pathology School of Dentistry São Paulo State University (UNESP), SPDepartment of Morphology Orthodontics and Pediatric Dentistry School of Dentistry São Paulo State University (UNESP), SPDepartment of Dental Materials and Prosthodontics School of Dentistry São Paulo State University (UNESP), SPDepartment of Restorative Dentistry School of Dentistry São Paulo State University (UNESP), SPDepartment of Physiology and Pathology School of Dentistry São Paulo State University (UNESP), SPUniversidade Estadual Paulista (UNESP)University of MichiganThe University of British Columbia (UBC)Anselmi, Caroline [UNESP]Mendes Soares, Igor Paulino [UNESP]Mota, Rafaella Lara Maia [UNESP]Leite, Maria LuísaRibeiro, Rafael Antonio de Oliveira [UNESP]Fernandes, Lídia de Oliveira [UNESP]Bottino, Marco C.de Souza Costa, Carlos Alberto [UNESP]Hebling, Josimeri [UNESP]2025-04-29T20:03:37Z2024-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3390/jfb15040097Journal of Functional Biomaterials, v. 15, n. 4, 2024.2079-4983https://hdl.handle.net/11449/30559710.3390/jfb150400972-s2.0-85191548280Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Functional Biomaterialsinfo:eu-repo/semantics/openAccess2025-04-30T14:32:09Zoai:repositorio.unesp.br:11449/305597Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-04-30T14:32:09Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Functionalization of PCL-Based Fiber Scaffolds with Different Sources of Calcium and Phosphate and Odontogenic Potential on Human Dental Pulp Cells
title Functionalization of PCL-Based Fiber Scaffolds with Different Sources of Calcium and Phosphate and Odontogenic Potential on Human Dental Pulp Cells
spellingShingle Functionalization of PCL-Based Fiber Scaffolds with Different Sources of Calcium and Phosphate and Odontogenic Potential on Human Dental Pulp Cells
Anselmi, Caroline [UNESP]
calcium
cell-homing therapy
phosphates
pulp capping agents
scaffolds
tissue engineering
title_short Functionalization of PCL-Based Fiber Scaffolds with Different Sources of Calcium and Phosphate and Odontogenic Potential on Human Dental Pulp Cells
title_full Functionalization of PCL-Based Fiber Scaffolds with Different Sources of Calcium and Phosphate and Odontogenic Potential on Human Dental Pulp Cells
title_fullStr Functionalization of PCL-Based Fiber Scaffolds with Different Sources of Calcium and Phosphate and Odontogenic Potential on Human Dental Pulp Cells
title_full_unstemmed Functionalization of PCL-Based Fiber Scaffolds with Different Sources of Calcium and Phosphate and Odontogenic Potential on Human Dental Pulp Cells
title_sort Functionalization of PCL-Based Fiber Scaffolds with Different Sources of Calcium and Phosphate and Odontogenic Potential on Human Dental Pulp Cells
author Anselmi, Caroline [UNESP]
author_facet Anselmi, Caroline [UNESP]
Mendes Soares, Igor Paulino [UNESP]
Mota, Rafaella Lara Maia [UNESP]
Leite, Maria Luísa
Ribeiro, Rafael Antonio de Oliveira [UNESP]
Fernandes, Lídia de Oliveira [UNESP]
Bottino, Marco C.
de Souza Costa, Carlos Alberto [UNESP]
Hebling, Josimeri [UNESP]
author_role author
author2 Mendes Soares, Igor Paulino [UNESP]
Mota, Rafaella Lara Maia [UNESP]
Leite, Maria Luísa
Ribeiro, Rafael Antonio de Oliveira [UNESP]
Fernandes, Lídia de Oliveira [UNESP]
Bottino, Marco C.
de Souza Costa, Carlos Alberto [UNESP]
Hebling, Josimeri [UNESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
University of Michigan
The University of British Columbia (UBC)
dc.contributor.author.fl_str_mv Anselmi, Caroline [UNESP]
Mendes Soares, Igor Paulino [UNESP]
Mota, Rafaella Lara Maia [UNESP]
Leite, Maria Luísa
Ribeiro, Rafael Antonio de Oliveira [UNESP]
Fernandes, Lídia de Oliveira [UNESP]
Bottino, Marco C.
de Souza Costa, Carlos Alberto [UNESP]
Hebling, Josimeri [UNESP]
dc.subject.por.fl_str_mv calcium
cell-homing therapy
phosphates
pulp capping agents
scaffolds
tissue engineering
topic calcium
cell-homing therapy
phosphates
pulp capping agents
scaffolds
tissue engineering
description This 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.
publishDate 2024
dc.date.none.fl_str_mv 2024-04-01
2025-04-29T20:03:37Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.3390/jfb15040097
Journal of Functional Biomaterials, v. 15, n. 4, 2024.
2079-4983
https://hdl.handle.net/11449/305597
10.3390/jfb15040097
2-s2.0-85191548280
url http://dx.doi.org/10.3390/jfb15040097
https://hdl.handle.net/11449/305597
identifier_str_mv Journal of Functional Biomaterials, v. 15, n. 4, 2024.
2079-4983
10.3390/jfb15040097
2-s2.0-85191548280
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Functional Biomaterials
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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