Abstract
The aim of this study was to evaluate the cytotoxic effect of the monomers isobutyl methacrylate (IBMA) and 1,6-hexanediol dimethacrylate (1,6-HDMA), the plasticizer di-n-butyl phthalate (DBP), and the degradation by-products methacrylic acid (MA) and benzoic acid (BA) on L929 cells. Based on previous investigations on the release of these compounds from hard chairside reline resins, a range of concentrations (micromol/L) were selected for the cytotoxicity tests (IBMA, 5.49-1406.57; 1,6-HDMA, 1.22-39.32; DBP, 1.12-143.8; MA, 9.07-581; BA, 3.19-409). Cytotoxic effects were assessed using MTT and (3)H-thymidine assays after the cells had been exposed to the test compounds at the given concentrations for 24 h. Cytotoxicity was rated based on cell viability relative to controls (cells exposed to medium without test substances). DNA synthesis activity was inhibited by all compounds. Mitochondrial dehydrogenase activity decreased in cells treated with monomers, plasticizer and MA by-product, whereas no cytotoxic effect was observed on contact with BA at the majority of concentrations tested. The ranges of suppression for (3)H-thymidine assay were: IBMA, 25-95%; 1,6-HDMA, 95-98%; DBP, 40-98%; MA, 97-99%; BA, 54-71%. For MTT assay, the...Continue Reading
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