Jiang Yao, Wang Jiang, Wang Yingwu, Li Hao, Fawcett J Paul, Gu Jingkai
Research Center for Drug Metabolism, College of Life Science, Jilin University, 130023 Changchun, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2007 May 1;850(1-2):564-8. doi: 10.1016/j.jchromb.2006.12.022. Epub 2006 Dec 22.
A rapid and sensitive method to determine colchicine in human plasma by liquid chromatography-tandem mass spectrometry (LC-MS/MS) has been developed. Colchicine and the internal standard (I.S.), tegafur, were extracted from the matrix with n-hexane:dichloromethane:isopropanol (300:150:15, v/v/v) and separated by reversed-phase high-performance liquid chromatography (HPLC) using formic acid:10 mM ammonium acetate:methanol (1:49:75, v/v/v) as the mobile phase in a run time of 2.5 min. Detection was carried out by electrospray positive ionization mass spectrometry in the multiple-reaction monitoring (MRM) mode. The assay was linear in the concentration range 0.050-10 ng/ml with intra- and inter-day precision (as relative standard deviation (R.S.D.)) of <2 and <7%, respectively. The method was applied to a pharmacokinetic study of colchicine in healthy volunteers given an oral dose of 2.0 mg.
已开发出一种通过液相色谱 - 串联质谱法(LC-MS/MS)测定人血浆中秋水仙碱的快速灵敏方法。秋水仙碱和内标替加氟从基质中用正己烷:二氯甲烷:异丙醇(300:150:15,v/v/v)萃取,并通过反相高效液相色谱(HPLC)分离,使用甲酸:10 mM醋酸铵:甲醇(1:49:75,v/v/v)作为流动相,运行时间为2.5分钟。通过电喷雾正离子质谱在多反应监测(MRM)模式下进行检测。该测定法在0.050 - 10 ng/ml的浓度范围内呈线性,日内和日间精密度(作为相对标准偏差(R.S.D.))分别<2%和<7%。该方法应用于口服2.0 mg秋水仙碱的健康志愿者的药代动力学研究。