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3D Graphene/silk fibroin scaffolds enhance dental pulp stem cell osteo/ odontogenic differentiation

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dc.contributor.author López-García, Sergio
dc.contributor.author Aznar-Cervantes, Salvador-D
dc.contributor.author Pagan, Ana
dc.contributor.author Llena, Carmen
dc.contributor.author Forner, Leopoldo
dc.contributor.author Sanz, José-L
dc.contributor.author García-Bernal, David
dc.contributor.author Sánchez-Bautista, Sonia
dc.contributor.author Ceballos, Laura
dc.contributor.author Fuentes, Victoria
dc.contributor.author Melo, María
dc.contributor.author Rodríguez-Lozano, Francisco-J
dc.contributor.author Onate-Sánchez, Ricardo-E
dc.date.accessioned 2025-10-20T14:40:19Z
dc.date.available 2025-10-20T14:40:19Z
dc.date.issued 2024-01
dc.identifier.citation López-García S, Aznar-Cervantes SD, Pagán A, Llena C, Forner L, Sanz JL, et al. 3D Graphene/silk fibroin scaffolds enhance dental pulp stem cell osteo/odontogenic differentiation. Dental Materials. marzo de 2024;40(3):431-40.
dc.identifier.issn 0109-5641
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/20482
dc.description.abstract Objectives: The current in vitro study aims to evaluate silk fibroin with and without the addition of graphene as a potential scaffold material for regenerative endodontics. Material and Methods: Silk fibroin (SF), Silk fibroin/graphene oxide (SF/GO) and silk fibroin coated with reduced graphene oxide (SF/rGO) scaffolds were prepared (n = 30). The microarchitectures and mechanical properties of scaffolds were evaluated using field emission scanning electron microscopy (FESEM), pore size and water uptake, attenuated total reflectance fourier transformed infrared spectroscopy (ATR-FTIR), Raman spectroscopy and mechanical compression tests. Next, the study analyzed the influence of these scaffolds on human dental pulp stem cell (hDPSC) viability, apoptosis or necrosis, cell adhesion, odontogenic differentiation marker expression and mineralized matrix deposition. The data were analyzed with ANOVA complemented with the Tukey post-hoc test (p < 0.005). Results: SEM analysis revealed abundant pores with a size greater than 50 nm on the surface of tested scaffolds, primarily between 50 nm and 600 m. The average value of water uptake obtained in pure fibroin scaffolds was statistically higher than that of those containing GO or rGO (p < 0.05). ATR-FTIR evidenced that the secondary structures did not present differences between pure fibroin and fibroin coated with graphene oxide, with a similar infrared spectrum in all tested scaffolds. Raman spectroscopy showed a greater number of defects in the links in SF/rGO scaffolds due to the reduction of graphene. In addition, adequate mechanical properties were exhibited by the tested scaffolds. Regarding biological properties, hDPSCs attached to scaffolds were capable of proliferating at a rate similar to the control, without affecting their viability over time. A significant upregulation of ALP , ON and DSPP markers was observed with SF/rGO and SF/GO groups. Finally, SF/GO and SF/rGO promoted a significantly higher mineralization than the control at 21 days. Significance: Data obtained suggested that SF/GO and SF/rGO scaffolds promote hDPSC differentiation at a genetic level, increasing the expression of key osteo/odontogenic markers, and supports the mineralization of the extracellular matrix. However, results from this study are to be interpreted with caution, requiring further in vivo studies to confirm the potential of these scaffolds.
dc.language.iso eng
dc.publisher ELSEVIER SCI LTD
dc.rights Atribución-NoComercial-SinDerivadas 3.0 España
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/3.0/es/ *
dc.subject.mesh Humans
dc.subject.mesh Fibroins/chemistry
dc.subject.mesh Tissue Scaffolds/chemistry
dc.subject.mesh Tissue Engineering/methods
dc.subject.mesh Graphite/chemistry
dc.subject.mesh Dental Pulp
dc.subject.mesh Cell Differentiation
dc.subject.mesh Water
dc.subject.mesh Cell Proliferation
dc.subject.mesh Stem Cells
dc.title 3D Graphene/silk fibroin scaffolds enhance dental pulp stem cell osteo/ odontogenic differentiation
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 38114344
dc.relation.publisherversion https://dx.doi.org/10.1016/j.dental.2023.12.009
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.1016/j.dental.2023.12.009
dc.journal.title Dental Materials
dc.identifier.essn 1879-0097


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