Teichert J, Kern J, Tritschler H J, Ulrich H, Preiss R
Institute of Clinical Pharmacology, University of Leipzig, Germany.
Int J Clin Pharmacol Ther. 1998 Dec;36(12):625-8.
The aim of the present study was to examine the pharmacokinetics of racemic alpha-lipoic acid in twelve healthy volunteers following single oral administration of 200 and 600 mg (Thioctacid 200 film tablets).
SUBJECTS, MATERIAL AND METHODS: Each film tablet contained 200 mg of alpha-lipoic acid. In addition, an injection solution containing 200 mg of alpha-lipoic acid was administered. Plasma concentrations of alpha-lipoic acid were determined using a validated reversed-phase HPLC method with electrochemical detection having a lower limit of quantitation of 1 ng/ml. The areas under curve (AUC) were 46.82 +/- 21.46 and 157.97 +/- 35.05 microg x min/ml for the oral and intravenous administration of 200 mg, respectively.
The AUC following oral administration of 600 mg was 157.83 +/- 35.82 microg x min/ml. The difference in mean t(1/2) for the two oral doses and the i.v. dose (in the range of 25.3-32.7 min) was not statistically significant.
The lack of a significant difference between values for apparent total plasma clearance for the 200 and 600 mg doses indicates non-saturable kinetics of alpha-lipoic acid in healthy volunteers in this dose range. The absolute bioavailability after the 200 mg dose was 29.1 +/- 10.3%.
本研究旨在检测200毫克和600毫克(硫辛酸200薄膜片)单剂量口服后,消旋α-硫辛酸在12名健康志愿者体内的药代动力学情况。
受试者、材料与方法:每片薄膜片含200毫克α-硫辛酸。此外,还给予含200毫克α-硫辛酸的注射溶液。采用经过验证的反相高效液相色谱法和电化学检测法测定血浆中α-硫辛酸的浓度,定量下限为1纳克/毫升。口服和静脉注射200毫克时的曲线下面积(AUC)分别为46.82±21.46和157.97±35.05微克·分钟/毫升。
口服600毫克后的AUC为157.83±35.82微克·分钟/毫升。两种口服剂量与静脉注射剂量的平均半衰期(在25.3 - 32.7分钟范围内)差异无统计学意义。
200毫克和600毫克剂量的表观总血浆清除率值之间无显著差异,表明在此剂量范围内,健康志愿者体内α-硫辛酸的动力学为非饱和动力学。200毫克剂量后的绝对生物利用度为29.1±10.3%。