Alpha and Beta Isomers of Tetrabromoethylcyclohexane (TBECH) Flame Retardant: Depletion and Metabolite Formation In Vitro Using a Model Rat Microsomal Assay

Abstract

The metabolism of α- and β-isomers of the flame retardant chemical tetrabromoethylcyclohexane (TBECH) was investigated using a model in vitro enzyme-mediated biotransformation assay based on rat liver microsomes. In enzymatically active assays, concentrations of both α- and β-TBECH isomers were equally depleted by about 40% and in a time-dependent fashion over a 60-min assay incubation period, and determined by GC-MS(ECNI) analysis. No such depletion was observed in nonenzymatically active control assays. After the full 60-min assay incubation period, debrominated TBECH metabolites were not detected by GC-MS(ECNI), and suggested that enzyme-mediated debromination of TBECH did not occur via cyctochrome P450 enzyme-mediated catalysis or that the rate of TBECH metabolism in vitro was too slow. In the enzymatically active assays, but not in the nonezymatically active control assays, α- and β-monohydroxy-TBECH (OH-TBECH), dihydroxy-TBECH ((OH)(2)-TBECH), and some additional compounds with molecular formulas of C(8)H(13)Br(3)O(2) and C(8)H(11)Br(3)O(2) were identified by LC-Q-ToF-MS. Two unique sets of OH-TBECH and (OH)(2)-TBECH metabolites were derived from both α- and β-TBECH isomers. The LC-ESI(-)-MS/MS peak areas of all four OH-TBECH and (OH)(2)-TBECH metabolites increased at a comparable rate in a time-dependent manner over a 60-min assay incubation period. This study demonstrated that metabolism via hydroxylation can occur in vitro for α- and β-TBECH. These results underscore the importance of understanding the biological fate of TBECH and the possible implications on the health and TBECH levels in exposed wildlife and in the environment.