Giacomini K M, Giacomini J C, Swezey S E, Harrison D C, Nelson W L, Burke T R, Blaschke T F
J Cardiovasc Pharmacol. 1980 Nov-Dec;2(6):825-32. doi: 10.1097/00005344-198011000-00011.
The disposition of d-, 1-, and d,1-disopyramide was studied in 5 conscious dogs after intravenous administration (15 mg/kg) of each compound using a balanced crossover design. The clearance of d-disopyramide (15.4 +/- 5.10 ml/min/kg) was significantly greater than that of the l-isomer (9.45 +/- 2.52 ml/min/kg) (p < 0.001). The clearance of the d,1-mixture was intermediate between that obtained for the d- and l-isomers. The steady-state volume of distribution of the three compounds was similar (approximately 1.4 liters/kg). The elimination half-life reflected differences in clearance, being 76.4 +/- 7.30 min for d-disopyramide, 112 +/- 23.4 min for 1-disopyramide, and 97.2 +/- 15.1 min for d,1-disopyramide. The effect of general anesthesia with urethane and chloralose on the disposition of the compounds was also examined. General anesthesia decreased the clearance and increased the half-life of all three compounds. No consistent differences in the volume of distribution were observed with anesthesia as compared to control. Thus, there is stereoselective elimination of the optical isomers of disopyramide in the dog, and general anesthesia decreases the clearance of d-, 1-, and d,1-disopyramide.
采用平衡交叉设计,对5只清醒犬静脉注射(15mg/kg)每种化合物后,研究了右旋、左旋和消旋双异丙吡胺的处置情况。右旋双异丙吡胺的清除率(15.4±5.10ml/min/kg)显著高于左旋异构体(9.45±2.52ml/min/kg)(p<0.001)。消旋混合物的清除率介于右旋和左旋异构体之间。三种化合物的稳态分布容积相似(约1.4升/kg)。消除半衰期反映了清除率的差异,右旋双异丙吡胺为76.4±7.30分钟,左旋双异丙吡胺为112±23.4分钟,消旋双异丙吡胺为97.2±15.1分钟。还研究了氨基甲酸乙酯和氯醛糖全身麻醉对化合物处置的影响。全身麻醉降低了所有三种化合物的清除率,延长了半衰期。与对照组相比,麻醉状态下未观察到分布容积的一致差异。因此,犬体内双异丙吡胺的光学异构体存在立体选择性消除,全身麻醉降低了右旋、左旋和消旋双异丙吡胺的清除率。