Heizmann P, Schmitt M, Leube J, Martin H, Saner A
Pharma Division, Nonclinical Development, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
J Chromatogr B Biomed Sci Appl. 1999 Jul 9;730(2):153-60. doi: 10.1016/s0378-4347(99)00146-2.
Reversed-phase HPLC procedures were developed for the determination of tolcapone (Ro 40-7592) and its metabolites Ro 40-7591, Ro 61-1448, and Ro 47-1669 in plasma and in urine samples. One of the procedures for plasma involved the determination of tolcapone and its metabolite Ro 40-7591 and the other, the determination of the two other metabolites. The urine assay enabled the simultaneous determination of tolcapone and all metabolites in one run. Sample preparation in plasma involved protein precipitation with acetonitrile. Urine was simply diluted. The compounds of interest were monitored in the UV at 270 nm. The limits of quantification were 0.05 microg/ml for each compound (plasma assay) and 0.2 microg/ml for the urine assay. The mean inter-assay precisions (C.V.) were < or = 6% (plasma assay) and < or = 8% (urine assay). The procedures were successfully applied to the sample analysis of animal pharmacokinetic (rat, dog, mouse, rabbit and cynomolgus monkey) and clinical pharmacology studies.
已开发出反相高效液相色谱法,用于测定血浆和尿液样本中的托卡朋(Ro 40 - 7592)及其代谢物Ro 40 - 7591、Ro 61 - 1448和Ro 47 - 1669。血浆分析的其中一种方法用于测定托卡朋及其代谢物Ro 40 - 7591,另一种方法用于测定另外两种代谢物。尿液分析可在一次运行中同时测定托卡朋和所有代谢物。血浆样本制备采用乙腈沉淀蛋白法。尿液只需稀释。在270 nm波长处用紫外光监测目标化合物。每种化合物的定量限为0.05微克/毫升(血浆分析)和0.2微克/毫升(尿液分析)。批间精密度均值(变异系数)分别为≤6%(血浆分析)和≤8%(尿液分析)。这些方法已成功应用于动物药代动力学(大鼠、狗、小鼠、兔子和食蟹猴)和临床药理学研究的样本分析。