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Multifunctional bilayer scaffold for dental pulp protection and sustained calcium hydroxide release for mineralized tissue regeneration

dc.contributor.authorAnselmi, Caroline [UNESP]
dc.contributor.authorMendes Soares, Igor P [UNESP]
dc.contributor.authorDal-Fabbro, Renan
dc.contributor.authorChang, Sarah
dc.contributor.authorde Carvalho, Ana Beatriz Gomes [UNESP]
dc.contributor.authorOliveira, Pedro H C [UNESP]
dc.contributor.authorDos Reis-Prado, Alexandre H
dc.contributor.authorde Souza Costa, Carlos A [UNESP]
dc.contributor.authorHebling, Josimeri [UNESP]
dc.contributor.authorBottino, Marco C
dc.date.accessioned2026-06-25T12:21:55Z
dc.date.issued2025-09-16
dc.description.abstractInjury to the mineralized tissues that protect the dental pulp can lead to pulp exposure and inflammation, necessitating the use of biologically active materials capable of preserving pulp vitality. While current biomaterials such as mineral trioxide aggregate (MTA) are widely used in vital pulp therapy (VPT), their high cost, challenging handling, and lack of structural flexibility highlight the need for alternatives. Here, we introduce a multifunctional bilayer scaffold composed of a polycaprolactone (PCL) film and a PCL/poly(ethylene oxide) (PCL/PEO) blend loaded with calcium hydroxide (CH), designed to provide both cytoprotection and mineralized tissue regeneration. The scaffold features a compact PCL layer, acting as a barrier to protect the pulp from external cytotoxic agents, and a CH-loaded fibrillar PCL/PEO electrospun layer, aimed at promoting odontoblastic differentiation through sustained calcium ion release. The bilayer structure demonstrated mechanical stability and a degradation profile suitable for clinical application. The release mechanism relies on gradual fiber degradation and CH dissolution. In vitro, the fibrillar layer enhanced calcium ion release, supported dental pulp stem cell adhesion and viability, and stimulated mineralized matrix formation. The compact layer preserved cell viability even in the presence of glass ionomer cement. In vivo, the bilayer scaffold elicited a comparable inflammatory response and expression of dentinogenesis and angiogenesis markers relative to MTA, although it did not attain the same level of mineralized tissue formation. Overall, our results indicate that this multifunctional bilayer scaffold offers a cost-effective, dual-purpose alternative to current materials, with potential for further optimization of its tissue regeneration capabilities prior to clinical implementation.
dc.description.affiliationDepartment of Cardiology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, USA; Department of Morphology and Pediatric Dentistry, São Paulo State University (UNESP), School of Dentistry, Araraquara, Brazil.
dc.description.affiliationDepartment of Cardiology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, USA; Department of Dental Materials and Prosthodontics, São Paulo State University (UNESP), School of Dentistry, Araraquara, Brazil.
dc.description.affiliationDepartment of Cardiology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.
dc.description.affiliationDepartment of Cardiology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, USA; Department of Dental Materials and Prosthodontics, São Paulo State University (UNESP), School of Dentistry, São José dos Campos, Brazil.
dc.description.affiliationDepartment of Cardiology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, USA; Department of Preventive and Restorative Dentistry, São Paulo State University (UNESP), School of Dentistry, Araçatuba, Brazil.
dc.description.affiliationDepartment of Cardiology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, USA; Department of Restorative Dentistry, Minas Gerais Federal University (UFMG), School of Dentistry, Belo Horizonte, Minas Gerais, Brazil.
dc.description.affiliationDepartment of Physiology and Pathology, São Paulo State University (UNESP), School of Dentistry, Araraquara, Brazil.
dc.description.affiliationDepartment of Morphology and Pediatric Dentistry, São Paulo State University (UNESP), School of Dentistry, Araraquara, Brazil.
dc.description.affiliationDepartment of Cardiology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, USA; Department of Biomedical Engineering, College of Engineering, University of Michigan, Ann Arbor, MI, USA. Electronic address: mbottino@umich.edu.
dc.description.affiliationUnespDepartment of Cardiology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, USA; Department of Morphology and Pediatric Dentistry, São Paulo State University (UNESP), School of Dentistry, Araraquara, Brazil.
dc.description.affiliationUnespDepartment of Cardiology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, USA; Department of Dental Materials and Prosthodontics, São Paulo State University (UNESP), School of Dentistry, Araraquara, Brazil.
dc.description.affiliationUnespDepartment of Cardiology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, USA; Department of Dental Materials and Prosthodontics, São Paulo State University (UNESP), School of Dentistry, São José dos Campos, Brazil.
dc.description.affiliationUnespDepartment of Cardiology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, USA; Department of Preventive and Restorative Dentistry, São Paulo State University (UNESP), School of Dentistry, Araçatuba, Brazil.
dc.description.affiliationUnespDepartment of Physiology and Pathology, São Paulo State University (UNESP), School of Dentistry, Araraquara, Brazil.
dc.description.affiliationUnespDepartment of Morphology and Pediatric Dentistry, São Paulo State University (UNESP), School of Dentistry, Araraquara, Brazil.
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1192913213
dc.identifier.dimensionspub.1192913213
dc.identifier.doi10.1016/j.biomaterials.2025.123700
dc.identifier.issn0142-9612
dc.identifier.issn1878-6979
dc.identifier.issn1878-5905
dc.identifier.orcid0000-0002-3189-1542
dc.identifier.orcid0000-0002-5748-5040
dc.identifier.orcid0000-0002-4125-8441
dc.identifier.orcid0000-0002-1263-1294
dc.identifier.orcid0000-0002-1593-7926
dc.identifier.orcid0000-0002-5866-7137
dc.identifier.orcid0000-0002-7455-6867
dc.identifier.orcid0000-0002-2846-2325
dc.identifier.orcid0000-0001-8740-2464
dc.identifier.pmcidPMC13033331
dc.identifier.pmid40974742
dc.identifier.urihttps://hdl.handle.net/11449/326589
dc.publisherElsevier
dc.relation.ispartofBiomaterials; v. 326; p. 123700
dc.rights.accessRightsAcesso abertopt
dc.rights.sourceRightsoa_all
dc.rights.sourceRightshybrid
dc.sourceDimensions
dc.titleMultifunctional bilayer scaffold for dental pulp protection and sustained calcium hydroxide release for mineralized tissue regeneration
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication8b3335a4-1163-438a-a0e2-921a46e0380d
relation.isOrgUnitOfPublication.latestForDiscovery8b3335a4-1163-438a-a0e2-921a46e0380d
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, São José dos Campospt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatubapt

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