Enquist M, Hermansson J
Apoteksbolaget AB, Central Laboratory, Department of Biomedicine, Stockholm, Sweden.
J Chromatogr. 1989 Sep 29;494:143-56. doi: 10.1016/s0378-4347(00)82664-x.
Two different high-performance liquid chromatographic systems for the determination of the total and free (R)- and (S)-disopyramide (DP) in plasma and urine were compared. In method I a Nucleosil C8 column was coupled in series with an alpha 1-acid glycoprotein column. Method II consisted of two systems; a LiChrosorb Si 60 column was used for the determination of the racemic drug concentration and the R/S ratio was determined on an alpha 1-acid glycoprotein column. The recovery of (R)- and (S)-DP from plasma was greater than 97% in both methods. The precisions of the (R)- and (S)-DP determinations in plasma are high with both methods. The relative standard deviations for the determination of the free concentration do not exceed 6.5% at 1.59 micrograms/ml racemic DP. Method II is preferred as it can also be used to determine the concentration of (R)- and (S)-monodesisopropyramide. It is also easier to avoid disturbances from endogenous compounds in plasma samples with method II than with method I. It was observed that DP was incorporated into urine sediment during storage. A simple ultrasonic treatment of the urine samples was demonstrated to release DP from the sediment.
比较了两种用于测定血浆和尿液中总(R)-和(S)-丙吡胺(DP)以及游离(R)-和(S)-丙吡胺的不同高效液相色谱系统。方法I中,将Nucleosil C8柱与α1-酸性糖蛋白柱串联。方法II由两个系统组成;使用LiChrosorb Si 60柱测定消旋药物浓度,并在α1-酸性糖蛋白柱上测定R/S比值。两种方法中,(R)-和(S)-DP从血浆中的回收率均大于97%。两种方法测定血浆中(R)-和(S)-DP的精密度都很高。在1.59微克/毫升消旋DP时,游离浓度测定的相对标准偏差不超过6.5%。首选方法II,因为它还可用于测定(R)-和(S)-单去异丙基丙吡胺的浓度。与方法I相比,使用方法II也更容易避免血浆样品中内源性化合物的干扰。观察到DP在储存期间会掺入尿沉渣中。已证明对尿样进行简单的超声处理可使DP从沉渣中释放出来。