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In Vitro Evaluation of Novel Calcium Silicate-Based and Resin-Modified Calcium Silicate Materials: Cytocompatibility and Mineralization Potential on Human Dental Pulp Stem Cells for Pulp Repair

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dc.contributor.author Rodríguez-Lozano, Francisco-Javier
dc.contributor.author Pérez-Guzman, Nuria
dc.contributor.author García-Ríos, Paula
dc.contributor.author García-Bernal, David
dc.contributor.author Lozano, Adrian
dc.contributor.author López-García, Sergio
dc.date.accessioned 2026-05-13T10:13:16Z
dc.date.available 2026-05-13T10:13:16Z
dc.date.issued 2026-06
dc.identifier.citation Rodríguez-Lozano FJ, Pérez-Guzmán N, García-Rios P, García-Bernal D, Lozano A, López-García S. In Vitro Evaluation of Novel Calcium Silicate-Based and Resin-Modified Calcium Silicate Materials: Cytocompatibility and Mineralization Potential on Human Dental Pulp Stem Cells for Pulp Repair. Microscopy Res & Technique. junio de 2026;89(6):932-47. doi:10.1002/jemt.70121
dc.identifier.issn 1059-910X
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/26397
dc.description.abstract This study aimed to evaluate the biological effects of three calcium silicate-based materials-Biodentine XP (BD-XP), TheraCal PT (THPT), and TheraBase Ca (THB)-on human dental pulp stem cells (hDPSCs), focusing on cytocompatibility, immunomodulatory behavior (via IL-6 expression), and odontogenic/mineralization potential compared to control conditions. hDPSCs were cultured with eluates (25%, 50%, 100%) of BD-XP, THPT, and THB. Cytocompatibility was assessed via metabolic activity assay, cell cycle analysis, and cell migration. Morphology and adhesion were examined by SEM, while surface composition was analyzed by EDX. IL-6 secretion was quantified using ELISA. Gene expression of odontogenic/osteogenic markers (ALP, DSPP, RUNX2, COL-1) was analyzed via qRT-PCR at 14 and 21 days. Alizarin Red S staining was used to assess mineralization. Results were compared to unconditioned and osteogenic controls (p < 0.05). All materials exhibited acceptable cytocompatibility. BD-XP promoted the highest cell viability, migration, and adhesion. IL-6 secretion was significantly reduced in all treated groups, most notably with THB. SEM and EDX showed strong cell attachment and calcium-rich surfaces for BD-XP. BD-XP significantly upregulated DSPP and RUNX2 at both time points and COL-1 at day 21. ALP expression was mainly observed in the positive control. BD-XP also showed the greatest mineralized nodule formation. Biodentine XP demonstrated the most favorable biological behavior, showing high cytocompatibility, upregulation of odontogenic markers, and enhanced mineralization. These results highlight its potential for clinical use in vital pulp therapy and regenerative endodontics.
dc.language.iso eng
dc.publisher WILEY
dc.rights Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es *
dc.subject.mesh Humans
dc.subject.mesh Calcium Compounds/pharmacology/chemistry
dc.subject.mesh Silicates/pharmacology/chemistry
dc.subject.mesh Dental Pulp/cytology/drug effects
dc.subject.mesh Stem Cells/drug effects/cytology
dc.subject.mesh Cells, Cultured
dc.subject.mesh Cell Movement/drug effects
dc.subject.mesh Biocompatible Materials/pharmacology/chemistry
dc.subject.mesh Osteogenesis/drug effects
dc.subject.mesh Interleukin-6/metabolism
dc.subject.mesh Cell Adhesion/drug effects
dc.subject.mesh Materials Testing
dc.subject.mesh Cell Differentiation/drug effects
dc.subject.mesh Cell Proliferation/drug effects
dc.subject.mesh Odontogenesis/drug effects
dc.title In Vitro Evaluation of Novel Calcium Silicate-Based and Resin-Modified Calcium Silicate Materials: Cytocompatibility and Mineralization Potential on Human Dental Pulp Stem Cells for Pulp Repair
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 41588682
dc.relation.publisherversion https://analyticalsciencejournals.onlinelibrary.wiley.com/doi/10.1002/jemt.70121
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.1002/jemt.70121
dc.journal.title Microscopy Research and Technique
dc.identifier.essn 1097-0029


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