Bisphenol
A (BPA) metabolism has been investigated using several in
vitro models, including human and rat liver microsomes
and subcellular (S9) fractions, as well as human-recombinant cytochrome P450 3A4 (CYP3A4)
expressed in Supersomes, for a comprehensive look at all possible
metabolic pathways. By an untargeted approach using liquid chromatography
coupled to a high-resolution quadrupole-time-of-flight mass spectrometer,
we were able to detect a large number of known Phase I and Phase II
metabolites of BPA, as well as several previously uncharacterized
ones. A detailed fragmentation study of BPA and its detected metabolites
was crucial to confirm structures. Isotope-labeled BPA analogs were
highly useful for the structural elucidation of many metabolites.
These results contribute to a better understanding of BPA metabolism,
including pathways that may introduce additional toxicity, as well
as help with the assessment of BPA exposure in different biological
matrices.