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以莫沙必利为内标,采用液相色谱-电喷雾串联质谱法测定人血浆中非索非那定的含量。

Quantification of fexofenadine in human plasma by liquid chromatography coupled to electrospray tandem mass spectrometry using mosapride as internal standard.

作者信息

Nirogi Ramakrishna V S, Kandikere Vishwottam N, Shukla Manoj, Mudigonda Koteshwara, Maurya Santosh, Komarneni Prashanth

机构信息

Biopharmaceutical Research, Suven Life Sciences Ltd, Serene Chambers, Road # 7, Banjara Hills, Hyderabad 500034, India.

出版信息

Biomed Chromatogr. 2007 Feb;21(2):209-16. doi: 10.1002/bmc.740.

Abstract

A rapid high-performance liquid chromatography/positive ion electrospray tandem mass spectrometry method was developed and validated for the quantification of fexofenadine in human plasma using mosapride as internal standard. Following solid-phase extraction, the analytes were separated using an isocratic mobile phase on a reverse-phase column and analyzed by MS/MS in the multiple reaction monitoring mode using the respective [M+H]+ ions, m/z 502/466 for fexofenadine and m/z 422/198 for the IS. The method exhibited a linear dynamic range of 1-500 ng/mL for fexofenadine in human plasma. The lower limit of quantification was 1 ng/mL with a relative standard deviation of less than 5% for fexofenadine. Acceptable precision and accuracy were obtained for concentrations over the standard curve range. The total chromatographic run time of 2 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

建立了一种快速高效液相色谱/正离子电喷雾串联质谱法,并以莫沙必利为内标对人血浆中非索非那定进行定量分析并验证。固相萃取后,在反相柱上使用等度流动相分离分析物,并在多反应监测模式下通过MS/MS使用各自的[M+H]+离子进行分析,非索非那定为m/z 502/466,内标为m/z 422/198。该方法在人血浆中非索非那定的线性动态范围为1-500 ng/mL。定量下限为1 ng/mL,非索非那定的相对标准偏差小于5%。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2分钟的总色谱运行时间使得每天能够分析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类血浆样品,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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