沈佳乐, 昝斌, 陈笑艳, 钟大放. LC-MS/MS法同时测定人血浆中福沙匹坦和代谢物阿瑞匹坦J. 药学学报, 2018,53(1): 121-126. doi: 10.16438/j.0513-4870.2017-0788
引用本文: 沈佳乐, 昝斌, 陈笑艳, 钟大放. LC-MS/MS法同时测定人血浆中福沙匹坦和代谢物阿瑞匹坦J. 药学学报, 2018,53(1): 121-126. doi: 10.16438/j.0513-4870.2017-0788
SHEN Jia-le, ZAN Bin, CHEN Xiao-yan, ZHONG Da-fang. Simultaneous determination of fosaprepitant and its metabolite aprepitant in human plasma by liquid chromatography-tandem mass spectrometryJ. Acta Pharmaceutica Sinica, 2018,53(1): 121-126. doi: 10.16438/j.0513-4870.2017-0788
Citation: SHEN Jia-le, ZAN Bin, CHEN Xiao-yan, ZHONG Da-fang. Simultaneous determination of fosaprepitant and its metabolite aprepitant in human plasma by liquid chromatography-tandem mass spectrometryJ. Acta Pharmaceutica Sinica, 2018,53(1): 121-126. doi: 10.16438/j.0513-4870.2017-0788

LC-MS/MS法同时测定人血浆中福沙匹坦和代谢物阿瑞匹坦

Simultaneous determination of fosaprepitant and its metabolite aprepitant in human plasma by liquid chromatography-tandem mass spectrometry

  • 摘要: 建立了LC-MS/MS法同时测定人血浆中福沙匹坦及其代谢物阿瑞匹坦,并应用于中国健康受试者的药动学研究。本法中血浆样品以乙腈沉淀蛋白处理,经Cortex C18+色谱柱(50 mm×2.1 mm,2.7 μm)分离,以甲醇-10 mmol·L-1醋酸铵(含0.1 mmol·L-1 EDTA)为流动相。采用电喷雾离子源(ESI源),以多反应监测负离子模式检测。以稳定同位素标记内标d4-福沙匹坦和d4-阿瑞匹坦分别作为福沙匹坦和阿瑞匹坦的内标,用于定量分析的离子反应分别为m/z 613.1→78.9(福沙匹坦)、m/z 617.0→78.9(d4-福沙匹坦)、m/z 533.2→275.1(阿瑞匹坦)和m/z 537.2→279.1(d4-阿瑞匹坦)。由于福沙匹坦为阿瑞匹坦的磷酸化前药,在血浆中快速降解,所以实验中采用碱性缓冲液处理血浆以确保其稳定。测定福沙匹坦标准曲线线性范围为15~6 000 ng·mL-1;测定阿瑞匹坦标准曲线线性范围为10~4 000 ng·mL-1。各待测物的日内、日间精密度和准确度均符合生物样品分析相关要求。该方法经验证后,成功应用于12名中国健康受试者静脉滴注150 mg福沙匹坦双葡甲胺后药动学研究。

     

    Abstract: An LC-MS/MS method was developed for the simultaneous determination of fosaprepitant and aprepitant in human plasma, and applied to a pharmacokinetic study of 150 mg fosaprepitant dimeglumine injection to 12 Chinese healthy volunteers. The analytes and internal standards were extracted from plasma by protein precipitation with acetonitrile and separated on a Cortex C18+ (50 mm×2.1 mm, 2.7 μm) column using a gradient elution procedure. Mass spectrometry was performed in negative MRM mode, and parent-to-produce transitions were as follows:m/z 613.1→78.9 for fosaprepitant, m/z 617.0→78.9 for d4-fosaprepitant, m/z 533.2→275.1 for aprepitant and m/z 537.2→279.1 for d4-aprepitant. Plasma sample was basified to stabilize fosaprepitant. The standard curves were demonstrated to be liner in the range of 15.0 to 6 000 ng·mL-1 for fosaprepitant and 10.0 to 4 000 ng·mL-1 for aprepitant. The intra-day precisions and inter-day precisions and accuracy were within the acceptable limits for all concentrations.

     

/

返回文章
返回