首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >A sensitive liquid chromatography-tandem mass spectrometry method for quantitative bioanalysis of fingolimod in human blood: Application to pharmacokinetic study
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A sensitive liquid chromatography-tandem mass spectrometry method for quantitative bioanalysis of fingolimod in human blood: Application to pharmacokinetic study

机译:一种敏感液相色谱 - 串联质谱法,用于人体血液分析Fingolimod分析:药代动力学研究的应用

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摘要

A simple and sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) method has been developed and validated for the determination of fingolimod in human blood. The analyte and internal standard fingolimod-d4 were extracted from 300 μl of human blood using protein precipitation coupled with solid-phase extraction method. The chromatographic separation was achieved with a Kinetex biphenyl column (100 x 4.6 mm, 2.6 μm) under isocratic conditions at the flow rate of 0.8 ml/min and column temperature was maintained at 45°C. The detection of analyte and internal standard was carried out by tandem mass spectrometry, operated in positive ion and multiple reaction monitoring acquisition mode. The method was fully validated for its selectivity, precision, accuracy, linearity, stability, detection and quantification limit. The extraction recovery of fingolimod in human blood ranged from 98.39 to 99.54%. The developed method was linear over the concentration range of 5-2500 pg/ml with a detection limit of 1 pg/ml. The developed method was validated and successfully applied for pharmacokinetic study after oral administration of fingolimod capsules.
机译:已经开发了一种简单而敏感的液相色谱 - 串联质谱(LC-MS / MS)方法并验证用于测定人体血液中的Fingolimod。使用蛋白质沉淀与固相萃取方法偶联的蛋白质沉淀从300μl人血液中提取分析物和内标Fingolimod-D4。通过在等离心条件下用KINETEX联烯基柱(100×4.6mm,2.6μm)在0.8ml / min的流速下进行色谱分离,在45℃下保持塔温。通过串联质谱法进行分析物和内标的检测,以正离子和多重反应监测采集模式操作。该方法完全验证了其选择性,精度,精度,线性度,稳定性,检测和量化极限。人类血液中Fingolimod的提取恢复范围从98.39%到99.54%。开发方法在5-2500pg / ml的浓度范围内线性,检测限为1 pg / ml。经过验证并成功地验证了开发的方法并成功地用于口服施用粉刺胶囊后的药代动力学研究。

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