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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Everolimus quantification in peripheral blood mononuclear cells using ultra high performance liquid chromatography tandem mass spectrometry
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Everolimus quantification in peripheral blood mononuclear cells using ultra high performance liquid chromatography tandem mass spectrometry

机译:超高效液相色谱串联质谱法定量检测外周血单个核细胞中的依维莫司

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摘要

A reliable ultra high performance liquid chromatography tandem mass spectrometry method has been developed for the determination of everolimus in human peripheral blood mononuclear cells (PBMCs). Protein precipitation was used for sample preparation. Analysis was performed on an UPLC Waters Acquity system. Chromatography was carried out using a cartridge column MassTrak TDM C18 (2.1 × 10. mm) with 0.1% formic acid and 2. mM of ammonium acetate in water and 0.1% formic acid and 2. mM of ammonium acetate in methanol mixture as a mobile phase delivered at a flow rate of 0.4. mL/min in gradient mode. The assay was linear over a range of 0-12.5. ng/mL. The analysis of quality control samples at 2.5, 5.0 and 10.0. ng/mL demonstrated good precision with relative standard deviation of less than 15%. Recoveries at concentrations of 2.5, 5.0 and 10.0. ng/mL were all greater than 83%. The method was successfully applied to the analysis of everolimus in PBMCs from blood samples of transplant recipients.
机译:已经开发了一种可靠的超高效液相色谱串联质谱法,用于测定人外周血单核细胞(PBMC)中的依维莫司。蛋白沉淀用于样品制备。分析在UPLC Waters Acquity系统上进行。色谱柱使用MassTrak TDM C18柱式色谱柱(2.1×10. mm)进行色谱分析,流动相为0.1%甲酸和2. mM乙酸铵的水溶液,以及0.1%甲酸和2. mM乙酸铵的甲醇混合物,相以0.4的流速输送。梯度模式下的mL / min。该测定在0-12.5范围内是线性的。 ng / mL。在2.5、5.0和10.0处进行质量控制样品的分析。 ng / mL表现出良好的精密度,相对标准偏差小于15%。浓度为2.5、5.0和10.0时的回收率。 ng / mL均大于83%。该方法已成功地用于分析移植受者血液样本中PBMC中的依维莫司。

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