Analysis of clozapine and norclozapine by high-performance liquid chromatography.

K K Akerman
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Abstract

A simple and reliable method for analyzing the concentrations of clozapine and its biologically active metabolite, norclozapine, in human serum or plasma has been developed. This method is based on reversed-phase high-performance liquid chromatography (HPLC) with automated solid-phase extraction (SPE). For HPLC analysis, samples and standards are prepared with an ASPEC automatic sample preparator using 100 mg Bond-Elut C18 SPE columns. The HPLC assay is an isocratic method with a mobile phase of acetonitrile-methanol-10 mM dipotassium hydrogenphosphate, pH 3.7 (30:2:100, v/v/v) at a flow-rate of 1.5 ml/min with a C8 reversed-phase column. Detection is performed with a diode array detector set at 220 nm and with peak purity analyses at 210-365 nm. The absolute recovery varied from 85 and 95%. The intra-assay coefficients of variation (C.V.s) were from 4.2 to 8.0% and the inter-assay C.V.s were from 1.1 to 9.3% at therapeutic drug concentrations. The detection limit is 15 nmol/l. The method has been developed for use in a clinical laboratory for therapeutic drug monitoring.

高效液相色谱法分析氯氮平和去氯氮平。
建立了一种简单可靠的分析人血清或血浆中氯氮平及其生物活性代谢物去甲氯氮平浓度的方法。该方法建立在反相高效液相色谱(HPLC)和自动固相萃取(SPE)的基础上。HPLC分析时,样品和标准品用ASPEC自动样品制备器制备,使用100 mg Bond-Elut C18固相萃取柱。高效液相色谱法:流动相为乙腈-甲醇-10 mM磷酸氢二钾,pH为3.7 (30:2:100,v/v/v), C8反相柱,流速为1.5 ml/min。检测是用二极管阵列检测器设置在220 nm和210-365 nm的峰值纯度分析进行的。绝对回收率在85% ~ 95%之间。在治疗药物浓度下,检测内变异系数为4.2 ~ 8.0%,检测间变异系数为1.1 ~ 9.3%。检出限为15 nmol/l。该方法已开发用于临床实验室治疗药物监测。
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