Loos W J, Sparreboom A, Verweij J, Nooter K, Stoter G, Schellens J H
Department of Medical Oncology, Rotterdam Cancer Institute (Daniel den Hoed Kliniek) and University Hospital Rotterdam, Netherlands.
J Chromatogr B Biomed Sci Appl. 1997 Jul 4;694(2):435-41. doi: 10.1016/s0378-4347(97)00117-5.
Two sensitive reversed-phase high-performance liquid chromatographic fluorescence methods, with simple sample handling at the site of the patient, are described for the determination of the lactone and lactone plus carboxylate forms of 9-aminocamptothecin (9AC). For 9AC lactone, the sample preparation was a liquid-liquid extraction with acetonitrile-n-butyl chloride (1:4, v/v), whereas the sample preparation for 9AC total (lactone plus carboxylate) was a simple deproteinization with 5% perchloric acid-methanol (1:1, v/v), which results in the conversion of the carboxylate into the lactone form. The lower limits of quantitation were 50 pg/ml and 100 pg/ml for 9AC lactone and 9AC total, respectively. The within-run precisions at four tested concentrations were < or = 6.3% for 9AC lactone and < or = 5.3% for 9AC total. The between-run precisions were < or = 8.9% and < or = 5.6%, respectively. The assays were developed to enable pharmacological analysis of 9AC in a bioavailability and oral phase I study in patients with solid tumors.
本文描述了两种灵敏的反相高效液相色谱荧光法,用于测定9-氨基喜树碱(9AC)的内酯形式以及内酯与羧酸盐形式之和,这两种方法在患者现场进行简单的样品处理即可。对于9AC内酯,样品制备采用乙腈-正丁基氯(1:4,v/v)液-液萃取;而对于9AC总量(内酯加羧酸盐),样品制备采用5%高氯酸-甲醇(1:1,v/v)进行简单的脱蛋白处理,这会使羧酸盐形式转化为内酯形式。9AC内酯和9AC总量的定量下限分别为50 pg/ml和100 pg/ml。在四个测试浓度下,9AC内酯的批内精密度≤6.3%,9AC总量的批内精密度≤5.3%。批间精密度分别≤8.9%和≤5.6%。这些分析方法旨在用于实体瘤患者的生物利用度和口服I期研究中9AC的药理学分析。