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Strontium-Doped Bioglass-Laden Gelatin Methacryloyl Hydrogels for Vital Pulp Therapy

dc.contributor.authorAminmansour, Sepideh
dc.contributor.authorGomes de Carvalho, Ana Beatriz [UNESP]
dc.contributor.authorMedeiros Cardoso, Lais [UNESP]
dc.contributor.authorAnselmi, Caroline [UNESP]
dc.contributor.authorRahimnejad, Maedeh
dc.contributor.authorDal-Fabbro, Renan
dc.contributor.authorBenavides, Erika
dc.contributor.authorCampos, Tiago Moreira Bastos
dc.contributor.authorBorges, Alexandre Luiz Souto [UNESP]
dc.contributor.authorBottino, Marco C.
dc.contributor.institutionUniversity of Michigan
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2025-04-29T20:17:22Z
dc.date.issued2024-04-01
dc.description.abstractThis study aimed to develop gelatin methacryloyl (GelMA)-injectable hydrogels incorporated with 58S bioactive glass/BG-doped with strontium for vital pulp therapy applications. GelMA hydrogels containing 0% (control), 5%, 10%, and 20% BG (w/v) were prepared. Their morphological and chemical properties were evaluated by scanning electron microscopy/SEM, energy dispersive spectroscopy/EDS, and Fourier transform infrared spectroscopy/FTIR (n = 3). Their swelling capacity and degradation ratio were also measured (n = 4). Cell viability (n = 8), mineralized matrix formation, cell adhesion, and spreading (n = 6) on DPSCs were evaluated. Data were analyzed using ANOVA/post hoc tests (α = 5%). SEM and EDS characterization confirmed the incorporation of BG particles into the hydrogel matrix, showing GelMA’s (C, O) and BG’s (Si, Cl, Na, Sr) chemical elements. FTIR revealed the main chemical groups of GelMA and BG, as ~1000 cm−1 corresponds to Si-O and ~1440 cm−1 to C-H. All the formulations were degraded by day 12, with a lower degradation ratio observed for GelMA+BG20%. Increasing the concentration of BG resulted in a lower mass swelling ratio. Biologically, all the groups were compatible with cells (p > 0.6196), and cell adhesion increased over time, irrespective of BG concentration, indicating great biocompatibility. GelMA+BG5% demonstrated a higher deposition of mineral nodules over 21 days (p < 0.0001), evidencing the osteogenic potential of hydrogels. GelMA hydrogels incorporated with BG present great cytocompatibility, support cell adhesion, and have a clinically relevant degradation profile and suitable mineralization potential, supporting their therapeutic potential as promising biomaterials for pulp capping.en
dc.description.affiliationDepartment of Cariology Restorative Sciences and Endodontics School of Dentistry University of Michigan
dc.description.affiliationDepartment of Dental Materials and Prosthodontics Sao Paulo State University, SP
dc.description.affiliationDepartment of Morphology and Pediatric Dentistry Sao Paulo State University, SP
dc.description.affiliationDepartment of Periodontics and Oral Medicine School of Dentistry University of Michigan
dc.description.affiliationDepartment of Prosthodontics and Periodontology Sao Paulo University, SP
dc.description.affiliationDepartment of Biomedical Engineering College of Engineering University of Michigan
dc.description.affiliationUnespDepartment of Dental Materials and Prosthodontics Sao Paulo State University, SP
dc.description.affiliationUnespDepartment of Morphology and Pediatric Dentistry Sao Paulo State University, SP
dc.identifierhttp://dx.doi.org/10.3390/jfb15040105
dc.identifier.citationJournal of Functional Biomaterials, v. 15, n. 4, 2024.
dc.identifier.doi10.3390/jfb15040105
dc.identifier.issn2079-4983
dc.identifier.scopus2-s2.0-85191591084
dc.identifier.urihttps://hdl.handle.net/11449/309968
dc.language.isoeng
dc.relation.ispartofJournal of Functional Biomaterials
dc.sourceScopus
dc.subjectbiocompatible materials
dc.subjectbioglass
dc.subjectdental pulp capping
dc.subjectgelatin
dc.subjecthydrogels
dc.subjectstrontium
dc.titleStrontium-Doped Bioglass-Laden Gelatin Methacryloyl Hydrogels for Vital Pulp Therapyen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0002-9886-8590[3]
unesp.author.orcid0000-0002-4125-8441[6]
unesp.author.orcid0000-0002-5707-7565[9]
unesp.author.orcid0000-0001-8740-2464[10]

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