Cytotoxicity of 35 dental resin composite monomers/additives in permanent 3T3 and three human primary fibroblast cultures
- 5 September 1998
- journal article
- research article
- Published by Wiley in Journal of Biomedical Materials Research
- Vol. 41 (3), 474-480
- https://doi.org/10.1002/(sici)1097-4636(19980905)41:3<474::aid-jbm18>3.0.co;2-i
Abstract
It was the purpose of this investigation to determine the cytotoxic effects (ED50 concentrations) of 35 monomers or additives identified in commercial dental resin composites. Monolayers of permanent 3T3 cells and three primary human fibroblast types derived from oral tissues (gingiva, pulp, and periodontal ligament) were used as test systems. All substances were tested in concentrations ranging from 0.01 to 5.0 mM. In general, ED50 values varied from 0.06 to >5 mM. Within the groups of co(monomers), initiators, and coinitiators, severe (e.g., Bis‐GMA, UDMA, DMBZ, and DMDTA) or moderate (HEMA, BEMA, CQ, DMPT, and DMAPE) cytotoxic effects could be evaluated. Within the group of reaction/decomposition products, only moderate or slight effects were found (ED50: 0.7 to >5 mM). The inhibitor BHT, the contaminant TPSb, and the photostabilizer HMBP, however, were highly cytotoxic in all cell cultures. In addition, the ED50 values of DBPO and HMBP significantly varied (0.43–3.8 mM, respectively, and 0.44–3.07 mM) with the applied cell culture. Our comprehensive screening shows that for several of the highly cytotoxic composite components, less cytotoxic alternatives are available. Furthermore, there was no cell type identified which was consistently less or more sensitive to the toxic effects of the tested compounds than the others. Primary human periodontal ligament and pulp fibroblasts, however, were found to be more sensitive than 3T3 and gingival fibroblasts to alterations from most tested substances. © 1998 John Wiley & Sons, Inc. J Biomed Mater Res, 41, 474–480, 1998.Keywords
This publication has 27 references indexed in Scilit:
- Determination of leachable components from four commercial dental composites by gas and liquid chromatography/mass spectrometryJournal of Dentistry, 1998
- Genotoxicity of dental materialsMutation Research/Genetic Toxicology, 1996
- Mutagenicity of dentin bonding agentsJournal of Biomedical Materials Research, 1994
- Elution of leachable components from compositesJournal of Oral Rehabilitation, 1994
- Qualitative analysis of dental resin composites by gas and liquid chromatography/mass spectrometryAnalytical and Bioanalytical Chemistry, 1994
- Local and Systemic Responses To Dental Composites and Glass IonomersAdvances in Dental Research, 1992
- Rate of elution of leachable components from compositeDental Materials, 1990
- Release of Formaldehyde from Dental CompositesJournal of Dental Research, 1988
- Hydrolytic Degradation of Dental CompositesJournal of Dental Research, 1984
- Compatibility of Various Materials with Oral Tissues. II: Pulp Responses to Composite IngredientsJournal of Dental Research, 1979