Shiqian Huang, Ding Yuan, Mengxiao Xu, Xuedong Bai, Chau Tin Yuet, Mariano Simón Pedano, James Kit Hon Tsoi, Dissanayaka Waruna Lakmal, Jun Wang, Xin Li
Within the limitation of this study, the FUDMA-based formulation exhibited favorable physicochemical properties, biocompatibility and bioactivity.
OBJECTIVES: To evaluate physicochemical properties, bioactivity and biocompatibility of experimental resin-modified calcium silicate cements (Rm-CSCs) formulated with BPA-free monomers (FUDMA and UDMA), in comparison with a BisGMA-based counterpart and commercial Rm-CSCs (TheraCal LC and BioCal-CAP).
METHODS: Experimental FUDMA-, UDMA-, and BisGMA-based Rm-CSCs were synthesized at a 3:5:2 mass ratio (resin matrix: tricalcium silicate: zirconia oxide). Calcium ion release and pH changes were tested over 28 days. Degree of conversion, water sorption, and solubility were assessed. Apatite-forming ability was examined after 28-day immersion in simulated body fluid (SBF) or culture medium. Cytotoxicity was determined using a CCK-8 assay with human dental pulp cells, and initial pulp response was assessed using a vital human tooth model. Data were analyzed using one-way ANOVA or Kruskal-Wallis test followed by Tukey's HSD test (α = 0.05).
RESULTS: All materials exhibited alkaline pH and sustained calcium ion release. Degree of conversion of FUDMA-, UDMA- and BisGMA-based formulations were 65.86%, 67.68% and 57.48%, respectively (p > 0.05). Water sorption of FUDMA- (36.22 μg/mm³) and UDMA-based cements (40.80 μg/mm³) were significantly lower than that of BisGMA-based counterpart (91.59 μg/mm³) (p < 0.05). Following SBF immersion, apatite-like calcium phosphate was formed for FUDMA-based version, other materials formed calcium carbonate as the main crystalline phase. Rm-CSCs were all cytocompatible, except TheraCal LC reduced cell viability to 42.60% (p < 0.05). Pulps capped with all Rm-CSCs maintained a well-organized morphology with no necrosis after 2 weeks.
SIGNIFICANCE: Within the limitation of this study, the FUDMA-based formulation exhibited favorable physicochemical properties, biocompatibility and bioactivity.