IADR Abstract Archives

Tricalcium Silicate Cements and the Consequences of Adding Resinous Components

Objective: Tricalcium silicate cements are self-setting materials on hydration currently used in direct pulp capping procedures mainly due to their biocompatibility and bioactivity. Light-cured tricalcium silicate materials aiming at reducing the setting time of this type of material were also developed. This work was designed to find out if adding resinous materials to tricalcium silicates would affect their biocompatibility.

Method: Pulp cells were isolated from human third molars by the outgrowth method and cultivated in MEM medium. Samples of BiodentineTM: a dentin substitute mainly composed of tricalcium silicates and TheraCal™LC: a light-cured composite material of calcium silicates and resinous components were prepared according to the manufacturers’ instructions. They were dipped into the culture media at 0.05 or 0.5 cm2/mL for 24 hours and 3 days (toxicity) or for 3, 5 and 7 days (proliferation) before applying the MTT test. Pro-inflammatory cytokine IL-8 was quantified by ELISA, after stimulating the cells with LTA for 4 hours and their incubation for additional 2 and 4 hours with media containing the materials eluates (0.05 cm2/mL). Untreated cells were used as controls.

Result: Increasing TheraCal™LC surface area from 0.05 to 0.5 cm2/mL significantly increased its toxicity from 20% to 40% respectively and significantly decreased pulp cell proliferation to reach less than 20% of the initial cell number (p<0.05). Biodentine™ had no significant toxicity nor affected cell proliferation. After LTA stimulation for 4 hours, IL-8 secretion in the presence of Biodentine™ conditioned medium was same as the control but that in presence of TheraCal™LC was twice higher than that with Biodentine™ (P<0.05).

Conclusion: Adding resinous components to tricalcium silicates induces toxic effects to target cells. They inhibit pulp cell proliferation and induce a significant secretion of IL-8 which might compromise the pulp regeneration capacity. Clinical significance: resin-based materials cannot be recommended for direct pulp capping.

Division: AADR/CADR Annual Meeting
Meeting: 2014 AADR/CADR Annual Meeting (Charlotte, North Carolina)
Location: Charlotte, North Carolina
Year: 2014
Final Presentation ID: 219
Abstract Category|Abstract Category(s): Pulp Biology & Regeneration Research
Authors
  • Strassler, Howard  ( University of Maryland, Baltimore, MD, USA )
  • About, Imad  ( Aix-Marseille Université, Marseille, , France )
  • Jeanneau, Charlotte  ( Aix-Marseille Université, Marseille, , France )
  • Chmilewsky, F  ( Aix-Marseille Université, Marseille, , France )
  • Brognart, M  ( Aix-Marseille Université, Marseille, , France )
  • Laurent, Patrick  ( Aix-Marseille Université, Marseille, , France )
  • SESSION INFORMATION
    Poster Session
    Pulp Biology & Regeneration Research I
    03/20/2014