¹Forensic Chemistry and Toxicology Department, Faculty of Health Sciences, Ankara University, Ankara, Turkey
²Pharmaceutical Toxicology Department, Faculty of Pharmacy, Ankara University, Ankara, Turkey
³Department of Endodontics, Gülhane Faculty of Dentistry, University of Health Sciences, Ankara, Turkey DOI : 10.29228/jrp.53 This study evaluated the in vitro cytotoxic, apoptotic and genotoxic effects of MTA, TheraCal and Dermabond (2-octyl cyanoacrylate) on L929 mouse fibroblast cells. Culture medium was exposed to the materials for 24 hours, 1 week and 2 weeks. Cells were seeded in 96 well plates with 5x103 cells/100 μL media per well for MTT assay, 6 well plates with 2x105 cells /2 mL media per well for comet assay,12-well plates with 2x105 cells/well for apoptosis assay and cells were exposed to the material eluates. The cell viability, genotoxicity and apoptotic status were evaluated by MTT, comet and apoptosis assays respectively at three different times (24 hours, 1 week and 2 weeks). There was no statistically significant difference (p˃0.05) between MTA and Dermabond at 24 hours, 1 week and 2 weeks exposures. However, TheraCal significantly reduced the cell viability at 1-week exposure to 66.70% (p˂0.05). TheraCal caused DNA damage at all exposures and there was a statistically significant difference (p˂0.05). According to flow cytometry results, TheraCal at 24-hour and 1-week showed significantly higher cytotoxic effects compared to MTA and Dermabond. No significant differences were detected between MTA and Dermabond. As observed from the current study it can be concluded that MTA and Dermabond are biocompatible capping materials in vital endodontic treatments. Since TheraCal exhibited cytotoxic and genotoxic effects caution should be exercised when it is being used. Keywords : L929 cells; cytotoxicity; genotoxicity; apoptosis; mta; theracal; dermabond