AIM: To study the stereoselective pharmacokinetics of the enantiomers
of metoprolol (Met). METHODS: The enantiomers of Met were metabolized
in isolated rat liver with hemoglubin-free medium. The enantiomers of
Met were analyzed with HPLC. RESULTS: The linear kinetics were found i
n 3 doses (0.16, 0.32, and 0.64 mg) of R-(+)- and S-(-)-Met. The time-
concentration curve of Met was fitted in first order-kinetics compartm
ent model, There were differences in the pharmacokinetic parameters (K
, T-1/2, and Cl) between the enantiomers at the same dose (P < 0.01).
The ratio of liver clearence of S-( -)-Met/R-( +)-Met was 0.14 -0.17.
CONCLUSION: Pharmacokinetics of enantiomers of Met in the isolated rat
liver were stereoselective, with a preferential clearance of R-( +)-M
et, which elimination was not saturable process.