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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of tulobuterol in rat plasma using a liquid chromatography-tandem mass spectrometry method and its application to a pharmacokinetic study of tulobuterol patch
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Determination of tulobuterol in rat plasma using a liquid chromatography-tandem mass spectrometry method and its application to a pharmacokinetic study of tulobuterol patch

机译:液相色谱-串联质谱法测定大鼠血浆中妥洛特罗的含量及其在妥洛特罗贴剂药代动力学研究中的应用

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摘要

A sensitive and accurate liquid chromatography-tandem mass spectrometry (LC-MS/MS) method has been developed and validated for determination of tulobuterol in rat plasma for the first time. Plasma samples were extracted by liquid-liquid extraction method with methyl tert-butyl ether and the analyte and clenbuterol (IS) were separated on a Venusil MP C-18 column (100mm x 2.1 mm, 3 mu m) using 0.1% formic acid-water-methanol as mobile phase, with a runtime of 5 min. The analyte was detected in multiple reaction monitoring (MRM) mode with positive electrospray ionization. Transitions of m/z 228.2 -> 154.0 for tulobuterol and m/z 277.1 -> 203.0 for the clenbuterol were monitored. The linear range was 0.5-100 ng/ml (r = 0.9967) for tulobuterol with the lower limit of quantitation of 0.5 ng/ml. The intra-day and inter-day precisions were less than 10.3% for the analyte and the accuracy was less than -8.6%. The RSD of matrix effect and recovery yield were within +/- 15% of nominal concentrations and tulobuterol was stable during stability studies. The validated method has been successfully applied to a pharmacokinetic study of three doses of tulobuterol patch in rats for the first time. (C) 2015 Elsevier B.V. All rights reserved.
机译:已开发出灵敏,准确的液相色谱-串联质谱(LC-MS / MS)方法,并首次验证了该方法可用于测定大鼠血浆中的妥洛特罗。通过液-液萃取法用甲基叔丁基醚萃取血浆样品,并在Venusil MP C-18色谱柱(100mm x 2.1 mm,3μm)上使用0.1%甲酸将分析物和盐酸克伦特罗(IS)分离,以水-甲醇为流动相,运行时间为5分钟。使用正电喷雾电离以多反应监测(MRM)模式检测分析物。监测盐酸妥布特罗的m / z 228.2-> 154.0和克仑特罗的m / z 277.1-> 203.0的跃迁。妥洛特罗的线性范围为0.5-100 ng / ml(r = 0.9967),定量下限为0.5 ng / ml。对于分析物,日内和日间精度小于10.3%,精度小于-8.6%。基质效应和回收率的RSD在标称浓度的+/- 15%以内,并且在稳定性研究期间妥洛特罗是稳定的。验证的方法已成功地首次成功应用于大鼠三剂量妥洛特罗贴剂的药代动力学研究。 (C)2015 Elsevier B.V.保留所有权利。

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