El. Kostoryz et al., In vitro toxicity of spiroorthocarbonate monomers designed for non-shrinking dental restoratives, J BIOM SC P, 11(2), 2000, pp. 187-196
In development of photopolymerized expanding monomers with epoxy resin syst
ems, there is a need for reactive expanding monomers that exert a good bioc
ompatibility profile. The objective of this study was to evaluate the in vi
tro toxicology of new spiroorthocarbonates designed to be expanding monomer
s. The expanding monomers investigated were: trans/trans-2,3,8,9-di(tetrame
thylene)-1,5,7,11-tetraoxaspiro[5,5]undecane (DTM-TOSU), 5,5-diethyl-19-oxa
dispiro-[1,3-dioxane-2,2'-1,3-dioxane-5',4'-bicyclo[4.1.0] heptane] (DECHE-
TOSU); 3,9-diethyl-3,9-dipropionyloxy methyl-1,5,7,11-tetraoxaspiro[5.5]und
ecane (DEDPM-TOSU); and 3,9-diethyl-3,9-diacetoxy methyl-1,5,7,11-tetraoxas
piro[5,5]undecane (DAMDE-TOSU). The in vitro toxicology of these monomers m
easured their cytotoxicity and mutagenicity potential. Succinic dehydrogena
se (SDH) activity in the MTT assay was used to assess the toxic dose that k
ills 50% of cells (TC50) for all the monomers. Their mutagenic potential wa
s measured in the Ames Salmonella assay with and without metabolic activati
on. Two solvents, DMSO and acetone, were used to validate effects. Appropri
ate controls included the solvents alone. All the expanding monomers in thi
s study were less cytotoxic than BISGMA (p < 0.01), a commercial component
of dental restoratives. The relative cytotoxicity of the expanding monomers
in DMSO was defined in the following order: DTM-TOSU (more toxic) > DECHE-
TOSU > DEDPM-TOSU > DAMDE-TOSU. Each was significantly different from the o
ther (p < 0.05). Overall, the TC50 values of all expanding monomers were si
gnificantly greater in DMSO than in acetone (p < 0.05). However, for BISGMA
this trend was opposite. For mutagenicity results, the expanding monomers
were non-mutagenic and there was no solvent effect on this outcome. The non
-mutagenicity and low cytotoxicity profile of these expanding monomers sugg
ests their potential for development of biocompatible non-shrinking composi
tes.