Hurtado-Sánchez María del Carmen, Acedo-Valenzuela María Isabel, Durán-Merás Isabel, Rodríguez-Cáceres María Isabel
Department of Analytical Chemistry, University of Extremadura, Badajoz, Spain.
J Sep Sci. 2015 Jun;38(11):1990-7. doi: 10.1002/jssc.201401443. Epub 2015 Apr 27.
Capillary electrophoresis was used for the rapid determination of three chemotherapeutic drugs employed to treat colorectal cancer: irinotecan, tegafur, and leucovorin, and their main metabolites (7-ethyl-10-hydroxycamptothecin and 5-fluorouracil), in human urine samples. A phosphate buffer (pH 11.34; 20 mM) was selected as the background electrolyte. A hydrodynamic injection (9 s, 30 mbar) was applied and the separation was carried out using a separation temperature and voltage of 25°C and 25 kV, respectively. A capillary with two detection windows for serial online UV and fluorescence detection was satisfactorily employed. A solid-supported liquid-liquid extraction procedure was optimized for the clean-up of the urine samples and the extraction of the analytes. Matrix effects were assessed and signal suppression was observed for three of the analytes, thus, matrix-matched calibration was used for compensating residual matrix effects on these analytes. The proposed method allows the separation and quantification of the chemotherapeutics in less than 6 min. Detection limits range between 0.01 and 0.30 mg/L. The method was satisfactorily applied to the determination of the target compounds in human urine samples, with recoveries of 92.4-107.7%.
伊立替康、替加氟和亚叶酸钙及其主要代谢物(7-乙基-10-羟基喜树碱和5-氟尿嘧啶)。选择磷酸盐缓冲液(pH 11.34;20 mM)作为背景电解质。采用流体动力学进样(9 s,30 mbar),分别在25°C的分离温度和25 kV的电压下进行分离。使用具有两个检测窗口的毛细管进行连续在线紫外和荧光检测,效果良好。优化了一种固载液-液萃取方法,用于尿液样本的净化和分析物的萃取。评估了基质效应,观察到三种分析物存在信号抑制,因此,采用基质匹配校准来补偿这些分析物上的残留基质效应。所提出的方法可在不到6分钟的时间内分离并定量测定化疗药物。检测限在0.01至0.30 mg/L之间。该方法成功应用于人尿液样本中目标化合物的测定,回收率为92.4 - 107.7%。