Spina E, Tomson T, Svensson J O, Faigle J W, Bertilsson L
Department of Clinical Pharmacology, Karolinska Institute, Huddinge University Hospital, Sweden.
Ther Drug Monit. 1988;10(4):382-5.
The kinetics of an enteric-coated formulation of carbamazepine-10,11-epoxide (CBZ-E) were studied in healthy subjects. A single oral dose of 100 mg of CBZ-E was given to eight subjects. Four of them were also given a single oral dose of 200 mg of CBZ-E. Plasma concentrations of CBZ-E and urinary excretion of the end metabolite trans-10,11-dihydroxy-10,11-dihydro-carbamazepine (trans-CBZ-diol) were determined by high performance liquid chromatography. Plasma kinetics of CBZ-E fitted an open one-compartment model with plasma elimination half-life of 7.4 +/- 1.8 h (mean +/- SD). The clearance was 105 +/- 17 ml/kg/h and the apparent volume of distribution 1.1 +/- 0.2 L/kg assuming complete bioavailability. There was no indication of dose-dependent elimination of CBZ-E. The recovery of trans-CBZ-diol in urine collected for 3 days was 67 +/- 9% of the given dose. This enteric-coated formulation may thus in the future be used for the evaluation of the clinical effects of CBZ-E in patients.
在健康受试者中研究了卡马西平-10,11-环氧化物(CBZ-E)肠溶包衣制剂的动力学。给8名受试者单次口服100mg的CBZ-E。其中4人还单次口服200mg的CBZ-E。通过高效液相色谱法测定CBZ-E的血浆浓度和终末代谢物反式-10,11-二羟基-10,11-二氢卡马西平(反式-CBZ-二醇)的尿排泄量。CBZ-E的血浆动力学符合开放一室模型,血浆消除半衰期为7.4±1.8小时(平均值±标准差)。假设生物利用度完全,清除率为105±17ml/kg/h,表观分布容积为1.1±0.2L/kg。没有迹象表明CBZ-E存在剂量依赖性消除。收集3天尿液中反式-CBZ-二醇的回收率为给药剂量的67±9%。因此,这种肠溶包衣制剂未来可能用于评估CBZ-E对患者的临床效果。