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采用液-液萃取法,建立灵敏的液相色谱串联质谱法测定人血浆中DPP-4抑制剂西他列汀的含量。

Sensitive liquid chromatography tandem mass spectrometry method for the quantification of sitagliptin, a DPP-4 inhibitor, in human plasma using liquid-liquid extraction.

作者信息

Nirogi Ramakrishna, Kandikere Vishwottam, Mudigonda Koteshwara, Komarneni Prashanth, Aleti Raghupathi, Boggavarapu Rajeshkumar

机构信息

Biopharmaceutical Research, Suven Life Sciences Ltd, Serene Chambers, Road-5, Avenue-7, Banjara Hills, Hyderabad 500034, India.

出版信息

Biomed Chromatogr. 2008 Feb;22(2):214-22. doi: 10.1002/bmc.926.

Abstract

A sensitive high-performance liquid chromatography-positive ion electrospray tandem mass spectrometry method was developed and validated for the quantification of sitagliptin, a DPP-4 inhibitor, in human plasma. Following liquid-liquid 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 408-235 for sitagliptin and m/z 310-148 for the internal standard. The assay exhibited a linear dynamic range of 0.1-250 ng/mL for sitagliptin in human plasma. The lower limit of quantification was 0.1 ng/mL with a relative standard deviation of less than 6%. Acceptable precision and accuracy were obtained for concentrations over the standard curve range. A run time of 2.0 min for each sample made it possible to analyze more than 300 human plasma samples per day. The validated method has been successfully used to analyze human plasma samples for application in pharmacokinetic studies.

摘要

建立并验证了一种灵敏的高效液相色谱-正离子电喷雾串联质谱法,用于定量测定人血浆中DPP-4抑制剂西他列汀。液-液萃取后,使用等度流动相在反相柱上分离分析物,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,西他列汀的m/z为408-235,内标的m/z为310-148。该测定法在人血浆中西他列汀的线性动态范围为0.1-250 ng/mL。定量下限为0.1 ng/mL,相对标准偏差小于6%。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2.0分钟,使得每天能够分析300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,以应用于药代动力学研究。

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