Microassay of propranolol enantiomers and conjugates in human plasma and urine by high-performance liquid chromatography after chiral derivatization for pharmacokinetic study.

A microdetermination of propranolol enantiomers and of their glucuronide and sulphate conjugates in human plasma and urine by reversed-phase HPLC after chiral derivatization is described. After extraction from 100 microliters of plasma or urine with racemic 4-methylpropranolol as internal standard (I.S.), the enantiomers are derivatized with R(+)-phenylethylisocyanate as chiral derivatization reagent. Chromatography is performed on Novapak C18 column with fluorescence detection. Glucuronide and sulphate conjugates are cleaved prior to extraction by incubating, respectively, the samples with glucuronidase-arylsulphatase and saccharic acid 1-4 lactone as specific glucuronidase inhibitor. The retention times of propranolol and I.S. enantiomer derivatives are short (tR = 5.5-6.2 min and 8.8-10.1 min, respectively). The diastereomeric derivatives are very stable and show good peak symmetry and resolutions (RS = 2 and 2.2). The use of 4-methylpropranolol as I.S. improves significantly relative standard deviations (RSD: 1.7-5.1). Sensitivity is about 1 ng ml-1 per enantiomer. The method is applied to pharmacokinetic studies of racemic propranolol in human plasma and urine. S-propranolol and its conjugates show higher concentrations than R-propranolol and its conjugates in plasma and urine.