首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Improved liquid chromatography-tandem mass spectrometry method for the analysis of eptifibatide in human plasma
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Improved liquid chromatography-tandem mass spectrometry method for the analysis of eptifibatide in human plasma

机译:改进的液相色谱-串联质谱法分析人血浆中的依替巴肽

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A rapid, selective and highly sensitive high performance liquid chromatography-tandem mass spectrometry method (LC-MS/MS) was developed and validated for the determination and pharmacokinetic investigation of eptifibatide in human plasma. Eptifibatide and the internal standard (IS), EPM-05, were extracted from plasma samples using solid phase extraction. Chromatographic separation was performed on a C_(18) column at a flow rate of 0.5mL/min. Detection of eptifibatide and the IS was achieved by tandem mass spectrometry with an electrospray ionization (ESI) interface in positive ion mode. Traditional multiple reaction monitoring (MRM) using the transition of m/z 832.6→m/z 646.4 and m/z 931.6→m/z 159.4 was performed to quantify eptifibatide and the IS, respectively. The calibration curves were linear over the range of 1-1000ng/mL with the lower limit of quantitation validated at 1ng/mL. The intra- and inter-day precisions were within 13.3%, while the accuracy was within ±7.6% of nominal values. The validated LC-MS/MS method was successfully applied for the evaluation of pharmacokinetic parameters of eptifibatide after intravenous (i.v.) administration of a 45μg/kg bolus of eptifibatide to 8 healthy volunteers.
机译:建立了一种快速,选择性和高度灵敏的高效液相色谱-串联质谱法(LC-MS / MS),该方法已用于人体血浆中依替巴肽的测定和药代动力学研究。使用固相萃取从血浆样品中萃取出依替巴肽和内标(IS)EPM-05。在C_(18)色谱柱上以0.5mL / min的流速进行色谱分离。依替巴肽和IS的检测是通过串联质谱在正离子模式下通过电喷雾电离(ESI)接口实现的。使用m / z 832.6→m / z 646.4和m / z 931.6→m / z 159.4的转变进行了传统的多反应监测(MRM),以分别定量依替巴肽和IS。校准曲线在1-1000ng / mL范围内呈线性,定量下限为1ng / mL。日内和日间精度在13.3%以内,而精度在标称值的±7.6%以内。经过验证的LC-MS / MS方法已成功地用于对8位健康志愿者静脉内(i.v.)给予45μg/ kg的安非他明大剂量推注后评估安非他明的药代动力学参数。

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