Piquette-Miller M, Jamali F
Faculty of Pharmacy & Pharmaceutical Sciences, University of Alberta, Edmonton, Canada.
Pharm Res. 1993 Feb;10(2):294-9. doi: 10.1023/a:1018907431893.
Nonstereospecific studies have indicated that the pharmacokinetics of propranolol (PR) are altered in inflammatory conditions such as arthritis. However, as the kinetics and dynamics of PR are stereoselective, we examined the effect of adjuvant arthritis (AA) on the disposition of the individual enantiomers. A novel normal-phase stereospecific HPLC assay for PR was developed involving chiral derivatization with S-(naphthyl)ethyl isocyanate and fluorescence detection. Oral and iv doses of racemic PR were administered to control and AA rats (n = 6). AA had no significant effect on either clearance or S:R ratio after iv doses. On the other hand, after oral doses, clearance was significantly decreased in AA. Although significant for both enantiomers, this effect was more pronounced on the less active R-enantiomer. The AUC R:S ratio was, therefore, significantly altered (AA, 14 +/- 3.0; control, 4.3 +/- 1.2). Increased total (S+R) plasma concentrations of PR in AA, possibly due to a reduced intrinsic clearance, therefore, reflect mainly increased concentrations of the less active R-enantiomer.
非立体特异性研究表明,普萘洛尔(PR)的药代动力学在诸如关节炎等炎症状态下会发生改变。然而,由于PR的动力学和药效学具有立体选择性,我们研究了佐剂性关节炎(AA)对各对映体处置的影响。我们开发了一种用于PR的新型正相立体特异性高效液相色谱法,该方法涉及用S-(萘基)乙基异氰酸酯进行手性衍生化和荧光检测。给对照大鼠和患AA的大鼠(n = 6)口服和静脉注射消旋PR。静脉注射剂量后,AA对清除率或S:R比值均无显著影响。另一方面,口服给药后,AA组的清除率显著降低。虽然对两种对映体均有显著影响,但这种影响在活性较低的R-对映体上更为明显。因此,AUC的R:S比值发生了显著改变(AA组为14±3.0;对照组为4.3±1.2)。AA组中PR的总(S+R)血浆浓度升高,可能是由于内在清除率降低,因此主要反映了活性较低的R-对映体浓度的增加。