Wang Zhe, Huang Cheng-ke, Sun Wei, Xiao Cui, Wang Zeng-shou
Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325027, China.
Biomed Chromatogr. 2015 Feb;29(2):188-93. doi: 10.1002/bmc.3257. Epub 2014 Jun 13.
A sensitive and rapid ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method was developed to determine voriconazole in human plasma. Sample preparation was accomplished through a simple one-step protein precipitation with methanol. Chromatographic separation was carried out on an Acquity UPLC BEH C18 column using an isocratic mobile phase system composed of acetonitrile and water containing 1% formic acid (45:55, v/v) at a flow rate of 0.50 mL/min. Mass spectrometric analysis was performed using a QTrap5500 mass spectrometer coupled with an electrospray ionization source in the positive ion mode. The multiple reaction monitoring transitions of m/z 351.0 → 281.5 and m/z 237.1 → 194.2 were used to quantify voriconazole and carbamazepine (internal standard), respectively. The linearity of this method was found to be within the concentration range of 2.0-1000 ng/mL with a lower limit of quantification of 2.0 ng/mL. Only 1.0 min was needed for an analytical run. This fully validated method was successfully applied to the pharmacokinetic study after oral administration of 200 mg voriconazole to 20 Chinese healthy male volunteers.
建立了一种灵敏、快速的超高效液相色谱串联质谱法(UPLC-MS/MS)用于测定人血浆中的伏立康唑。样品制备通过用甲醇进行简单的一步蛋白沉淀来完成。色谱分离在Acquity UPLC BEH C18柱上进行,使用由乙腈和含1%甲酸的水(45:55,v/v)组成的等度流动相系统,流速为0.50 mL/min。质谱分析使用QTrap5500质谱仪,结合电喷雾电离源,采用正离子模式。分别使用m/z 351.0→281.5和m/z 237.1→194.2的多反应监测跃迁来定量伏立康唑和卡马西平(内标)。该方法的线性范围为2.0 - 1000 ng/mL,定量下限为2.0 ng/mL。一次分析运行仅需1.0分钟。该经过充分验证的方法成功应用于20名中国健康男性志愿者口服200 mg伏立康唑后的药代动力学研究。