Wu Yingli, Mao Zhengsheng, Liu Youping, Wang Xin, Di Xin
Laboratory of Drug Metabolism and Pharmacokinetics, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, PR China.
Laboratory of Drug Metabolism and Pharmacokinetics, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, PR China.
J Pharm Biomed Anal. 2015 Oct 10;114:216-21. doi: 10.1016/j.jpba.2015.05.020. Epub 2015 Jun 11.
A rapid and sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for simultaneous determination of febuxostat and its three active metabolites in human plasma was developed using a ZORBAX SB-C18 column (50 mm × 4.6 mm, 5 μm) and an optimized gradient mobile phase consisting of acetonitrile, water and formic acid. Plasma samples were spiked with the internal standard losartan and then pre-treated using one-step protein precipitation with methanol. Mass spectrometric detection was performed by selective reaction monitoring mode via electrospray ionization source operating in positive ionization mode. The method exhibited good linearity over the concentration range of 10-20,000 ng/mL for febuxostat, 1.0-270 ng/mL for 67M-1 and 67M-2, and 0.8-250 ng/mL for 67 M-4, respectively. The intra- and inter-day precisions were less than 14.7% and the accuracy ranged from -4.3% to 5.1%. The method was successfully applied to a clinical pharmacokinetic study of febuxostat in humans after oral administration of a single dose of febuxostat at 40, 80 and 120 mg.
建立了一种快速灵敏的液相色谱-串联质谱(LC-MS/MS)法,用于同时测定人血浆中的非布司他及其三种活性代谢物。该方法采用ZORBAX SB-C18色谱柱(50 mm×4.6 mm,5μm)和由乙腈、水和甲酸组成的优化梯度流动相。血浆样品加入内标氯沙坦后,用甲醇一步沉淀蛋白进行预处理。质谱检测采用选择性反应监测模式,通过电喷雾电离源在正离子模式下运行。该方法在非布司他浓度范围为10-20,000 ng/mL、67M-1和67M-2浓度范围为1.0-270 ng/mL、67M-4浓度范围为0.8-250 ng/mL时均表现出良好的线性。日内和日间精密度均小于14.7%,准确度范围为-4.3%至5.1%。该方法成功应用于单剂量40、80和120 mg非布司他口服给药后人的临床药代动力学研究。