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新型抗肿瘤药物N-苯甲酰基星形孢菌素(CGP 41 251)及四种潜在代谢产物在微量血浆中的高效液相色谱分析

High-performance liquid chromatographic analysis of the new antitumour drug N-benzoylstaurosporine (CGP 41 251) and four potential metabolites in micro-volumes of plasma.

作者信息

van Gijn R, Havik E, Boven E, Vermorken J B, ten Bokkel Huinink W W, van Tellingen O, Beijnen J H

机构信息

Department of Pharmacy, Slotervaart Hospital/Netherlands Cancer Institute, Amsterdam.

出版信息

J Pharm Biomed Anal. 1995 Dec;14(1-2):165-74. doi: 10.1016/0731-7085(95)01616-3.

Abstract

A high-performance liquid chromatographic (HPLC) assay is described for the determination of the new antitumour drug N-benzoylstaurosporine (CGP 41 251; I) and four of its potential metabolites in micro-volumes (100 microliters) of plasma. After addition of an internal standard, the compounds were isolated from plasma by liquid-liquid extraction with diisopropyl ether. Chromatography was carried out using a 5 microns LiChrospher C-18 end-capped column (125 x 4.0 mm i.d.) and binary gradient elution with acetonitrile and a triethylamine-containing phosphate buffer (pH 3.6) as solvents. Fluorimetric detection was performed with excitation and emission wavelengths set at 286 and 386 nm, respectively. The absolute recovery was more than 98% for all of the investigated compounds. The limit of detection (LOD) for I and three metabolites was 0.1 ng ml-1 and the lower limit of quantitation (LLQ) was 0.2 ng ml-1 in 100 microliters of plasma. The LOD and LLQ for the fourth metabolite was 0.25 and 0.5 ng ml-1, respectively. The between-day and within-day precisions were always < 15% for all the analytes. A limited pharmacokinetic study in mice treated and with I demonstrated that the method is appropriate for this purpose.

摘要

本文描述了一种高效液相色谱(HPLC)分析法,用于测定新型抗肿瘤药物N-苯甲酰基星形孢菌素(CGP 41 251;I)及其四种潜在代谢物在微量(100微升)血浆中的含量。加入内标后,通过用二异丙醚进行液-液萃取从血浆中分离出这些化合物。使用5微米的LiChrospher C-18封端柱(内径125×4.0毫米),以乙腈和含三乙胺的磷酸盐缓冲液(pH 3.6)作为溶剂进行二元梯度洗脱。荧光检测分别在激发波长和发射波长设置为286和386纳米的条件下进行。所有研究化合物的绝对回收率均超过98%。在100微升血浆中,I和三种代谢物的检测限(LOD)为0.1纳克/毫升,定量下限(LLQ)为0.2纳克/毫升。第四种代谢物的LOD和LLQ分别为0.25和0.5纳克/毫升。所有分析物的日间和日内精密度始终<15%。在接受I治疗的小鼠中进行的有限药代动力学研究表明该方法适用于此目的。

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