Barilero I, Gandia D, Armand J P, Mathieu-Boué A, Ré M, Gouyette A, Chabot G G
Laboratoire de Pharmacologie Clinique (URA 147 CNRS, U 140 INSERM), Institut Gustave-Roussy, Villejuif, France.
J Chromatogr. 1992 Mar 27;575(2):275-80. doi: 10.1016/0378-4347(92)80156-k.
CPT-11 (I; 7-ethyl-10-[4-(1-piperidino)-1- piperidino]carbonyloxycamptothecin) is a new anticancer agent currently under clinical development. A sensitive high-performance liquid chromatographic assay suitable for the simultaneous determination of I and its active metabolite SN-38 (II) in human plasma, and their preliminary clinical pharmacokinetics, are described. Plasma samples were processed using a solid-phase (C18) extraction step allowing mean recoveries of I, II and the internal standard camptothecin (III) of 84, 99 and 72%, respectively. The extracts were chromatographed on a C18 reversed-phase column with a mobile phase composed of acetonitrile, phosphate buffer and heptanesulphonic acid, with fluorescence detection. The calibration graphs were linear over a wide range of concentrations (1 ng/ml-10 micrograms/ml), and the lower limit of determination was 1 ng/ml for both I and II. The method showed good precision: the within-day relative standard deviation (R.S.D.) (5-1000 ng/ml) was 13.0% (range 4.9-19.4%) for I and 12.8% (6.7-19.1%) for II; the between-day R.S.D. (5-10,000 ng/ml was 7.9% (5.4-17.5%) for I and 9.7% (3.5-15.1%) for II. Using this assay, plasma pharmacokinetics of both I and II were simultaneously determined in three patients receiving 100 mg/m2 I as a 30-min intravenous infusion. The mean peak plasma concentration of I at the end of the intravenous infusion was 2400 +/- 285 ng/ml (mean +/- standard error of the mean). Plasma decay was triphasic with half-lives alpha, beta and gamma of 5.4 +/- 1.8 min, 2.5 +/- 0.5 h and 20.2 +/- 4.6 h, respectively. The volume of distribution at steady state was 105 +/- 15 l/m2, and the total body clearance was 12.5 +/- 1.9 l/h.m2. The maximum concentrations of the active metabolite II reached 36 +/- 11 ng/ml.
CPT - 11(I;7 - 乙基 - 10 - [4 - (1 - 哌啶基)-1 - 哌啶基]羰基氧喜树碱)是一种目前正在进行临床开发的新型抗癌药物。本文描述了一种灵敏的高效液相色谱法,该方法适用于同时测定人血浆中的I及其活性代谢物SN - 38(II),并介绍了它们初步的临床药代动力学情况。血浆样品通过固相(C18)萃取步骤进行处理,I、II和内标喜树碱(III)的平均回收率分别为84%、99%和72%。萃取物在C18反相柱上进行色谱分析,流动相由乙腈、磷酸盐缓冲液和庚烷磺酸组成,并采用荧光检测。校准曲线在很宽的浓度范围内(1 ng/ml - 10 μg/ml)呈线性,I和II的测定下限均为1 ng/ml。该方法具有良好的精密度:I在日内相对标准偏差(R.S.D.)(5 - 1000 ng/ml)为13.0%(范围4.9 - 19.4%),II为12.8%(6.7 - 19.1%);日间R.S.D.(5 - 10,000 ng/ml)I为7.9%(5.4 - 17.5%),II为9.7%(3.5 - 15.1%)。使用该测定法,在3例接受100 mg/m² I静脉输注30分钟的患者中同时测定了I和II的血浆药代动力学。静脉输注结束时I的平均血浆峰浓度为2400±285 ng/ml(平均值±平均值的标准误差)。血浆衰减呈三相,α、β和γ半衰期分别为5.4±1.8分钟、2.5±0.5小时和20.2±4.6小时。稳态分布容积为105±15 l/m²,全身清除率为12.5±1.9 l/h·m²。活性代谢物II的最大浓度达到36±11 ng/ml。