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液相色谱-串联质谱法测定血浆中 JAK2 抑制剂 CYT387。

Liquid chromatography-tandem mass spectrometric assay for the JAK2 inhibitor CYT387 in plasma.

机构信息

Utrecht University, Faculty of Science, Department of Pharmaceutical Sciences, Division of Pharmacoepidemiology & Clinical Pharmacology, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2012 May 1;895-896:174-7. doi: 10.1016/j.jchromb.2012.03.021. Epub 2012 Mar 23.

Abstract

A quantitative bioanalytical liquid chromatography-tandem mass spectrometric (LC-MS/MS) assay for the JAK2 inhibitor CYT387 was developed and validated. Plasma samples were pre-treated using protein precipitation with acetonitrile containing cediranib as internal standard. The extract was directly injected into the chromatographic system after dilution with water. This system consisted of a sub-2 μm particle, trifunctional bonded octadecyl silica column with a gradient using 0.005% (v/v) of formic acid in a mixture of water and methanol. The eluate was transferred into the electrospray interface with positive ionization and the analyte was detected in the selected reaction monitoring mode of a triple quadrupole mass spectrometer. The assay was validated in a 0.25-1000 ng/ml calibration range. Within day precisions were 3.0-13.5%, between day precisions 5.7% and 14.5%. Accuracies were between 96% and 113% for the whole calibration range. The drug was stable under all relevant analytical conditions. Finally, the assay was successfully used to assess drug levels in mice.

摘要

建立并验证了一种用于 JAK2 抑制剂 CYT387 的定量生物分析液相色谱-串联质谱(LC-MS/MS)检测法。使用含 Cediranib 的乙腈进行蛋白沉淀预处理血浆样品,以内标物形式加入。提取液经水稀释后直接注入色谱系统。该系统采用亚 2μm 粒径、三官能键合十八烷基硅胶柱,以水和甲醇混合物中 0.005%(v/v)的甲酸为流动相进行梯度洗脱。洗脱液被转移到电喷雾接口,采用正离子化方式,并在三重四极杆质谱的选择反应监测模式下检测分析物。该检测法在 0.25-1000ng/ml 的校准范围内进行了验证。日内精密度为 3.0-13.5%,日间精密度为 5.7%-14.5%。整个校准范围内的准确度在 96%-113%之间。药物在所有相关分析条件下均稳定。最后,该检测法成功用于评估小鼠体内的药物水平。

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