Species differences in the chirality of the carbonyl reduction of [14C] fenofibrate in laboratory animals and humans

Publisher Website
Google Scholar
Abstract
The prochiral carbonyl group of fenofibrate (isopropyl 2‐[4‐(4‐chlorobenzoyl)phenoxy]‐2‐methyl propionate) is reduced during its metabolism giving rise to a chiral secondary alcohol, “reduced fenofibric acid.” Chiral and diastereomeric HPLC methods have been developed for the determination of its enantiomeric composition and these have been applied to the measurement of the “reduced fenofibric acid” enantiomers in urine of rats, guinea pigs, dogs, and human volunteers given [14C]fenofibrate. In the three animal species, the reduction is markedly enantioselective for the (–)‐isomer, the enantiomeric ratios (–/ +) being 95:5. This was not due to differences in the excretion of the enantiomers, since when racemic “reduced fenofibric acid” was given to rats it was recovered in the urine with the same enantiomeric composition as the dose form. In humans the ratio was 52:48 showing the lack of stereoselectivity of reduction in this species.