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Biomineralization potential and biological properties of a new tantalum oxide (Ta2O5)-containing calcium silicate cement

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dc.contributor.author Rodríguez-Lozano, Francisco-Javier
dc.contributor.author Lozano, A
dc.contributor.author López-García, S
dc.contributor.author García-Bernal, David
dc.contributor.author Sanz, José-Luis
dc.contributor.author Guerrero-Gironés, Julia
dc.contributor.author Llena, Carmen
dc.contributor.author Forner, Leopoldo
dc.contributor.author Melo, María
dc.date.accessioned 2025-11-18T09:26:27Z
dc.date.available 2025-11-18T09:26:27Z
dc.date.issued 2022-02
dc.identifier.citation Rodríguez-Lozano FJ, Lozano A, López-García S, García-Bernal D, Sanz JL, Guerrero-Gironés J, et al. Biomineralization potential and biological properties of a new tantalum oxide (Ta2O5)¿containing calcium silicate cement. Clin Oral Invest. febrero de 2022;26(2):1427-41.
dc.identifier.issn 1432-6981
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/20714
dc.description.abstract OBJECTIVE: The present study evaluated the biological effects and biomineralization potential of a new tantalum oxide (Ta(2)O(5))-containing material designed for vital pulp therapy or perforation repair (NeoMTA 2), compared to NeoMTA Plus and Bio-C Repair. MATERIAL AND METHODS: Human dental pulp stem cells (hDPSCs) were exposed to different eluates from NeoMTA Plus, NeoMTA 2, and Bio-C Repair. Ion release from each material was determined using inductively coupled plasma-optical emission spectrometry (ICP-MS). The biological experiments performed were MTT assays, apoptosis/necrosis assays, adhesion assays, migration assays, morphology evaluation, and reactive oxygen species (ROS) production analysis. Biomineralization was assessed by Alizarin red S staining. Finally, osteo/odontogenic gene expression was determined by real-time quantitative reverse-transcriptase polymerase chain reaction (RT-qPCR). Data were analyzed using one-way ANOVA followed by Tukey's multiple comparison test. RESULTS: NeoMTA 2 displayed a significantly higher calcium release compared to the other materials (p-<-0.05). When hDPSCs were cultured in presence of the different material eluates, all groups exhibited similar hDPSC viability and migration rates when compared to untreated cells. Substantial cell attachment and spreading were observed in all materials' surfaces, without significant differences. hDPSCs treated with NeoMTA 2 displayed an upregulation of ALP, Col1A1, RUNX2 (p-<-0.001), ON, and DSPP genes (p-<-0.05), and showed the highest mineralization potential compared to other groups (p-<-0.001). Finally, the more concentrated eluates from these materials, specially NeoMTA Plus and NeoMTA 2, promoted higher ROS production in hDPSCs compared to Bio-C Repair and control cells (p-<-0.001), although these ROS levels did not result in increased cell death. CONCLUSIONS: The new tantalum oxide (Ta(2)O(5))-containing material shows an adequate cytocompatibility and the ability to promote biomineralization without using chemical osteogenic inducers, showing great potential as a new material for vital pulp therapy. CLINICAL RELEVANCE: NeoMTA 2 seems to be a promising material for vital pulp therapy. Further studies considering its biocompatibility and biomineralization potential are necessary.
dc.language.iso eng
dc.publisher Springer Heidelberg
dc.subject.mesh Biomineralization
dc.subject.mesh Calcium
dc.subject.mesh Calcium Compounds/pharmacology
dc.subject.mesh Cell Differentiation
dc.subject.mesh Cells, Cultured
dc.subject.mesh Dental Pulp
dc.subject.mesh Humans
dc.subject.mesh Materials Testing
dc.subject.mesh Oxides
dc.subject.mesh Silicate Cement
dc.subject.mesh Silicates/pharmacology
dc.subject.mesh Stem Cells
dc.subject.mesh Tantalum
dc.title Biomineralization potential and biological properties of a new tantalum oxide (Ta2O5)-containing calcium silicate cement
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 34382106
dc.relation.publisherversion https://link.springer.com/10.1007/s00784-021-04117-x
dc.identifier.doi 10.1007/s00784-021-04117-x
dc.journal.title Clinical Oral Investigations
dc.identifier.essn 1436-3771


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