Bondiolotti G P, Pollera C, Pirola R, Bareggi S R
Department of Pharmacology Chemotherapy and Medical Toxicology, School of Medicine, University of Milan, Italy.
J Chromatogr B Analyt Technol Biomed Life Sci. 2006 Jun 6;837(1-2):87-91. doi: 10.1016/j.jchromb.2006.04.014. Epub 2006 May 22.
This paper describes a method of determining clioquinol levels in hamster plasma and tissue by means of HPLC and electrochemical detection. Clioquinol was separated on a Nucleosil C18 300 mm x 3.9 mm i.d. 7 microm column at 1 ml/min using a phosphate/citrate buffer 0.1M (400 ml) with 600 ml of a methanol:acetonitrile (1:1, v/v) mobile phase. The retention times of clioquinol and the IS were, respectively, 11.6 and 8.1 min; the quantitation limit (CV>8%) was 5 ng/ml in plasma and 10 ng/ml in tissues. The intra- and inter-assay accuracies of the method were more than 95%, with coefficients of variation between 3.0 and 7.7%, and plasma and tissue recovery rates of 72-77%. There was a linear response to clioquinol 5-2000 ng/ml in plasma, and 10-1000 ng/g in tissues. The method is highly sensitive and selective, makes it possible to study the pharmacokinetics of plasma clioquinol after oral administration and the distribution of clioquinol in tissues, and could be used to monitor plasma clioquinol levels in humans.
本文描述了一种通过高效液相色谱法(HPLC)和电化学检测来测定仓鼠血浆和组织中氯碘羟喹水平的方法。氯碘羟喹在Nucleosil C18 300 mm×3.9 mm内径、7微米的色谱柱上进行分离,流速为1 ml/min,使用0.1M的磷酸盐/柠檬酸盐缓冲液(400 ml)与600 ml甲醇:乙腈(1:1,v/v)的流动相。氯碘羟喹和内标的保留时间分别为11.6分钟和8.1分钟;血浆中的定量限(CV>8%)为5 ng/ml,组织中的定量限为10 ng/ml。该方法的批内和批间准确度均超过95%,变异系数在3.0%至7.7%之间,血浆和组织回收率为72 - 77%。血浆中氯碘羟喹浓度在5 - 2000 ng/ml之间、组织中氯碘羟喹浓度在10 - 1000 ng/g之间呈线性响应。该方法具有高灵敏度和高选择性,能够研究口服给药后血浆氯碘羟喹的药代动力学以及氯碘羟喹在组织中的分布情况,可用于监测人体血浆中氯碘羟喹的水平。