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RESEARCH PRODUCT

Biocompatibility of three new calcium silicate-based endodontic sealers on human periodontal ligament stem cells.

Mar Collado-gonzálezAdrián LozanoR. E. Oñate-sánchezLeopoldo FornerP. S. Ortolani-seltenerichDavid García-bernalCarmen LlenaFrancisco Javier Rodríguez-lozano

subject

Mineral trioxide aggregateBiocompatibilityPeriodontal ligament stem cellsPeriodontal LigamentDentistry02 engineering and technologyCell morphologyEndodonticsRoot Canal Filling Materials03 medical and health sciences0302 clinical medicineCell MovementMaterials TestingPeriodontal fiberHumansMTT assayViability assayGeneral DentistryCells CulturedCell Proliferationbusiness.industryCell growthChemistrySilicatesStem Cells030206 dentistryCalcium Compounds021001 nanoscience & nanotechnologyMolecular biology0210 nano-technologybusiness

description

Aim To evaluate the biocompatibility of three calcium silicate-based endodontic sealers, Bioroot BC Sealer (Septodont, Saint-Maur-des-Fosses, France), Endoseal MTA (EndoSeal, Maruchi, Seoul, Korea) and Nano-ceramic Sealer (B&L Biotech, Fairfax, VA, USA) (NCS), on human periodontal ligament stem cells (hPDLSCs). Methodology Human periodontal ligament stem cells were cultured in the presence of various endodontic sealer eluates for 24 h. Cell viability was determined using the MTT assay. Cell death and changes in phenotype induced by the set endodontic sealer eluates were evaluated through flow cytometry. Also, an in vitro scratch wound-healing model was used to determine their effects in cell migration. Finally, to assess cell morphology and attachment to the different sealers, hPDLSCs were directly seeded onto the material surfaces and analysed by scanning electron microscopy (SEM). One-way analysis of variance (anova) followed by a Bonferroni post-test was performed (P < 0.05). Results At 24 h, cell spreading was evident in the presence of Bioroot BC Sealer (BR) and Nano-ceramic Sealer (NCS), but not Endoseal MTA (ES). At 72 h, BR and NCS exhibited high and moderate cell proliferation, respectively, whereas ES revealed low rates of cell proliferation (P < 0.05). Similar results were obtained in a cell death assay. In addition, hPDLSCs maintained their mesenchymal phenotype in all conditions although their capacity to migrate was higher in the presence of BR. Finally, SEM studies revealed a good degree of proliferation, cell spreading and attachment, especially when using BR and NCS discs. Conclusions BR and NCS were associated with better cytocompatibility than ES. Further in vitro and in vivo investigations are required to confirm the suitability of these calcium silicate-based endodontic sealers for clinical application.

10.1111/iej.12703https://pubmed.ncbi.nlm.nih.gov/27666949