Functionalization of PCL-Based Fiber Scaffolds with Different Sources of Calcium and Phosphate and Odontogenic Potential on Human Dental Pulp Cells
Autor(a) principal: | |
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Data de Publicação: | 2024 |
Outros Autores: | , , , , , , , |
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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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 |
_version_ |
1834482432356646912 |