Analysis of the cytotoxicity and bioactivity of CeraSeal, BioRoot™ and AH Plus ® sealers in pre-osteoblast lineage cells

Background The objective of the present study was to evaluate in vitro the cytotoxicity and bioactivity of various endodontic sealers (CeraSeal, BioRoot™ and AH Plus ® ) in pre-osteoblast mouse cells (MC3T3 cells). Methods MC3T3 cells (ATCC CRL-2594) were plated in 1 × 10 4 cells/well in 96-well plates in contact with endodontic sealers at concentrations of 1:10 and 1:100. Cell viability was evaluated by MTT assay after 24 and 48 h. In addition, sealer bioactivity was measured by RT-PCR for mediator of inflammation ( Tnf, Ptgs2 ) and mineralization ( Runx2, Msx1, Ssp1 and Dmp1 ) after 24 h and by Alizarin Red S Assay of mineralization after 28 days. Data were analyzed using one-way ANOVA followed by the Tukey’s post-test at a significance level of 5%. Results BioRoot™ presented 24-hour cytotoxicity ( p < 0.05) at 1:10 concentration. In the period of 48 h, no endodontic cement was cytotoxic to the cells compared to the control ( p > 0.05). TNF-α gene expression was induced by AH Plus ® ( p < 0.05), while Ptgs2 was induced by the CeraSeal and BioRoot™ ( p < 0.05). The expression of Runx2 was stimulated by BioRoot™ and AH Plus ® ( p < 0.05). In contrast, the expression of Dmp-1 Dmp1 was higher for the CeraSeal and BioRoot™ ( p < 0.05). Nonetheless, the sealers did not impact the formation of mineralization nodules ( p > 0.05). Conclusion CeraSeal, BioRoot™ and AH Plus ® sealers were not cytotoxic to MC3T3 cells within 48 h, but differentially induced the expression of genes related to inflammation and mineralization without impacting biomineralization by the cells.