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采用灵敏的液相色谱/串联质谱法对人血浆中的氯吡格雷进行定量分析。

Quantification of clopidogrel in human plasma by sensitive liquid chromatography/tandem mass spectrometry.

作者信息

Nirogi Ramakrishna V S, Kandikere Vishwottam N, Shukla Manoj, Mudigonda Koteshwara, Maurya Santosh, Boosi Ravikumar

机构信息

Biopharmaceutical Research, Suven Life Sciences Ltd., Serene Chambers, Road # 7, Banjara Hills, Hyderabad 500 034, India.

出版信息

Rapid Commun Mass Spectrom. 2006;20(11):1695-700. doi: 10.1002/rcm.2497.

Abstract

A simple, sensitive and rapid high-performance liquid chromatography/positive electrospray ionization tandem mass spectrometry method was developed and validated for the assay of clopidogrel in human plasma. Following liquid-liquid extraction, the analytes were separated using an isocratic mobile phase on a reversed-phase column and analyzed by mass spectrometry in the multiple reaction monitoring mode using the respective M+H ions, m/z 322/212 for clopidogrel and m/z 264/154 for the internal standard. The assay exhibited a linear dynamic range of 5-6000 pg/mL for clopidogrel in human plasma. The lower limit of quantification was 5 pg/mL with a relative standard deviation of less than 8%. Acceptable precision and accuracy were obtained for concentrations over the standard curve range. A run time of 2.5 min for each sample made it possible to analyze more than 400 human plasma samples per day. The validated method has been successfully used to analyze human plasma samples for application in pharmacokinetic, bioavailability or bioequivalence studies.

摘要

建立了一种简单、灵敏、快速的高效液相色谱/正电喷雾电离串联质谱法,并对其进行了验证,用于测定人血浆中的氯吡格雷。液-液萃取后,使用等度流动相在反相柱上分离分析物,并采用多反应监测模式通过质谱法分析,使用各自的M+H离子,氯吡格雷的为m/z 322/212,内标的为m/z 264/154。该测定法在人血浆中氯吡格雷的线性动态范围为5-6000 pg/mL。定量下限为5 pg/mL,相对标准偏差小于8%。在标准曲线范围内的浓度获得了可接受的精密度和准确度。每个样品的运行时间为2.5分钟,使得每天能够分析400多个人类血浆样品。该经过验证的方法已成功用于分析人血浆样品,以用于药代动力学、生物利用度或生物等效性研究。

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