In vitro and in vivo human metabolism and pharmacokinetics of S ‐ and R‐praziquantel

This study aimed at investigating the metabolism of R‐ and S‐PZQ as this could have implications on efficacy and safety of racemate and R‐PZ Q specific formulations under development. In vitro CYP reaction phenotyping assay using 10 recombinant CYP (rCYP) isoenzymes showed hepatic CYP1A2, 2C19, 2D6, 3A4, and 3A5 were the major enzymes involved in metabolism of PZQ. Enzyme kinetic studies were performed by substrate depletion and metaboli te formation methods, by incubating PZQ and its R‐ or S‐enantiomers in human liver microsomes (HLM) and the rCYP enzymes. The effect of selective CYP inhibitors on PZQ metabolism was assessed in HLM. CYP1A2, 2C19, and 3A4 exhibited different catalytic activity toward PZQ, R‐ and S‐enantiomer s. Metabolism of R‐PZQ was mainly catalyzed by CYP1A2 and CYP2C19, whereas metabolism of S‐PZQ was mainly by CYP2C19 and CYP3A4. Based on metabolic CLint obtained through formation of hydroxylated metabolites, CYP3A4 was estimated to contribute 89.88% to metabolism of S ‐PZQ using SIMCYP® IVIVE prediction. Reanalysis of samples from a human PZQ ‐ketoconazole (KTZ) drug‐drug interaction pharmacokinetic study confirmed these findings in that KTZ, a potent inhibitor of CYP3A, selectively increased area under the curve of S‐PZQ by 68% and that of R‐PZQ by just 9%. Knowledge of enantioselective metabolism will enable better understandin g of variable efficacy of PZQ in patients and the R‐PZQ formulation under development.
Source: Pharmacology Research and Perspectives - Category: Drugs & Pharmacology Authors: Tags: ORIGINAL ARTICLE Source Type: research