Li Shuijun, Liu Gangyi, Jia Jingying, Liu Yun, Pan Cheng, Yu Chen, Cai Yongbao, Ren Jianying
Central Laboratory, Shanghai Xuhui Central Hospital, Shanghai 200031, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2007 Mar 1;847(2):174-81. doi: 10.1016/j.jchromb.2006.10.013. Epub 2006 Nov 20.
A simple, accurate and selective LC-MS/MS method was developed and validated for simultaneous quantification of ten antiarrhythic drugs (diltiazem, amiodarone, mexiletine, propranolol, sotalol, verapamil, bisoprolol, metoprolol, atenolol, carvedilol) and a metabolite (norverapamil) in human plasma. Plasma samples were simply pretreated with acetonitrile for deproteinization. Chromatographic separation was performed on a Capcell C(18) column (50mmx2.0mm, 5microm) using a gradient mixture of acetonitrile and water (both containing 0.02% formic acid) as a mobile phase at flow rate of 0.3ml/min. The analytes were protonated in the positive electrospray ionization (ESI) interface and detected in multiple reaction monitoring (MRM) mode. Calibration curves were linear over wide ranges from sub- to over-therapeutic concentration in plasma for all analytes. Intra- and inter-batch precision of analysis was <12.0%, accuracy ranged from 90% to 110%, average recovery from 85.0% to 99.7%. The validated method was successfully applied to therapeutic drug monitoring (TDM) of antiarrhythic drugs in routine clinical practice.
建立并验证了一种简单、准确且具选择性的液相色谱-串联质谱法,用于同时定量测定人血浆中的十种抗心律失常药物(地尔硫卓、胺碘酮、美西律、普萘洛尔、索他洛尔、维拉帕米、比索洛尔、美托洛尔、阿替洛尔、卡维地洛)及一种代谢物(去甲维拉帕米)。血浆样品仅用乙腈进行预处理以去除蛋白质。色谱分离在Capcell C(18)柱(50mm×2.0mm,5μm)上进行,使用乙腈和水(均含0.02%甲酸)的梯度混合物作为流动相,流速为0.3ml/min。分析物在正电喷雾电离(ESI)界面中质子化,并在多反应监测(MRM)模式下进行检测。所有分析物的校准曲线在血浆中亚治疗浓度至超治疗浓度的宽范围内呈线性。分析的批内和批间精密度<12.0%,准确度范围为90%至110%,平均回收率为85.0%至99.7%。该验证方法成功应用于常规临床实践中抗心律失常药物的治疗药物监测(TDM)。