Wang Mengye, Xiang Ping, Yan Hui, Shen Baohua, Shen Min
Department of Forensic Medicine, Shanghaii Medical College, Fudan University, Shanghai 200032, China.
Se Pu. 2008 Jan;26(1):10-4.
A method was developed for the determination of endogenous steroids in urine using liquid chromatography-tandem mass spectrometry (LC-MS/MS) with methyltestosterone as internal standard. After enzymatic hydrolysis by beta-glucuronidase and liquid-liquid extraction, the urine sample was chromatographed on a Cosmosil C18 column with a mixture of methanol and ammonium acetate-formic acid (68:32, v/v) as mobile phase, then detected using MS/MS system with electrospray ionization (ESI) in multi-reaction monitoring (MRM) mode. The detection limits ranged from 0.01 ng/mL to 10 ng/mL. The recoveries ranged from 96.7% to 106.5%, and the intra- and inter-day precisions (measured as relative standard deviations) were less than 7% and 11%, respectively. With simple and fast sample preparation, the method was sensitive and specific for simultaneous determination of these 5 kinds of endogenous steroids in urine. The method has been successfully applied in pharmacokinetic study and is thus a potential alternative for gas chromatography-mass spectrometry (GC-MS) based procedures in routine analysis of endogenous steroids such as DHEA in human urine.
建立了一种以甲基睾酮为内标,采用液相色谱 - 串联质谱法(LC-MS/MS)测定尿液中内源性甾体类化合物的方法。尿液样品经β-葡萄糖醛酸酶酶解及液 - 液萃取后,在Cosmosil C18柱上进行色谱分离,以甲醇和醋酸铵 - 甲酸(68:32,v/v)的混合液为流动相,然后采用电喷雾电离(ESI)的MS/MS系统在多反应监测(MRM)模式下进行检测。检测限为0.01 ng/mL至10 ng/mL。回收率为96.7%至106.5%,日内和日间精密度(以相对标准偏差衡量)分别小于7%和11%。该方法样品制备简单快速,对尿液中这5种内源性甾体类化合物的同时测定具有灵敏性和特异性。该方法已成功应用于药代动力学研究,因此在人尿中脱氢表雄酮等内源性甾体类化合物的常规分析中,是基于气相色谱 - 质谱法(GC-MS)的方法的一种潜在替代方法。