Huizing M T, Sparreboom A, Rosing H, van Tellingen O, Pinedo H M, Beijnen J H
Department of Medical Oncology, Antoni van Leeuwenhoek Hospital/Netherlands Cancer Institute, Amsterdam.
J Chromatogr B Biomed Appl. 1995 Dec 15;674(2):261-8. doi: 10.1016/0378-4347(95)00308-8.
A reversed-phase high-performance liquid chromatographic (HPLC) method has been validated for the quantitative determination of the three major paclitaxel metabolites (6 alpha-hydroxypaclitaxel, 3'-p-hydroxypaclitaxel, 6 alpha,3'-p-dihydroxypaclitaxel) in human plasma. The HPLC system consists of an APEX-octyl analytical column and acetonitrile-methanol-0.02 M ammonium acetate buffer pH 5 (AMW; 4:1:5, v/v/v) as the mobile phase. Detection is performed by UV absorbance measurement at 227 nm. The sample pretreatment of the plasma samples involves solid-phase extraction (SPE) on Cyano Bond Elut columns. The concentrations of the metabolic products could be determined by using the paclitaxel standard curve with a correction factor of 1.14 for 6 alpha,3'-p-dihydroxypaclitaxel. The recoveries of paclitaxel and the metabolites 6 alpha,3'-p-dihydroxypaclitaxel, 3'-p-hydroxypaclitaxel and 6 alpha-hydroxypaclitaxel in human plasma were 89, 78, 91 and 89%, respectively. The accuracy of the assay for the determination of paclitaxel and its metabolites varied between 95 and 97%, at a 50 ng/ml analyte concentration. The lower limit of quantitation was 10 ng/ml for both the parent drug and its metabolites.
已验证一种反相高效液相色谱(HPLC)方法,用于定量测定人血浆中三种主要的紫杉醇代谢物(6α-羟基紫杉醇、3'-对羟基紫杉醇、6α,3'-对二羟基紫杉醇)。HPLC系统由一根APEX-辛基分析柱和乙腈-甲醇-0.02M醋酸铵缓冲液pH5(AMW;4:1:5,v/v/v)作为流动相组成。通过在227nm处测量紫外吸光度进行检测。血浆样品的预处理包括在氰基键合硅胶柱上进行固相萃取(SPE)。代谢产物的浓度可以通过使用紫杉醇标准曲线来确定,其中6α,3'-对二羟基紫杉醇的校正因子为1.14。紫杉醇以及代谢物6α,3'-对二羟基紫杉醇、3'-对羟基紫杉醇和6α-羟基紫杉醇在人血浆中的回收率分别为89%、78%、91%和89%。在分析物浓度为50ng/ml时,测定紫杉醇及其代谢物的方法准确度在95%至97%之间。母体药物及其代谢物的定量下限均为10ng/ml。