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采用液相色谱/串联质谱法同时定量测定人血浆中棕榈酸地塞米松和地塞米松。

Simultaneous quantitation of dexamethasone palmitate and dexamethasone in human plasma by liquid chromatography/tandem mass spectrometry.

作者信息

Yang Yan, Li Hao, Gao Kan, Liu Mingyuan, Sun Yantong, Yan Tingting, Fawcett J Paul, Cui Yimin, Gu Jingkai

机构信息

Research Center for Drug Metabolism, College of Life Science, Jilin University, Changchun 130021, PR China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2008 Feb 1;862(1-2):119-24. doi: 10.1016/j.jchromb.2007.11.033. Epub 2007 Dec 4.

Abstract

A rapid and sensitive liquid chromatography/tandem mass spectrometry (LC/MS/MS) method for simultaneous quantitation of dexamethasone palmitate and dexamethasone in human plasma was developed. After sample preparation by protein precipitation and liquid-liquid extraction, the analytes and internal standard (IS) were separated on a Venusil XBP-C8 column using gradient elution. Multiple reaction monitoring of dexamethasone palmitate, dexamethasone and IS used the precursor to product ion transitions at m/z 631.8-->373.1, m/z 393.2-->147.1 and m/z 264.2-->58.1, respectively. The method was linear over the ranges 1.5-1000ng/mL for dexamethasone palmitate and 2.5-250ng/mL for dexamethasone with intra- and inter-day precisions of <10% and accuracies of 100+/-7%. The assay was applied to a clinical pharmacokinetic study involving the injection of dexamethasone palmitate to healthy volunteers.

摘要

建立了一种快速灵敏的液相色谱/串联质谱(LC/MS/MS)法,用于同时定量测定人血浆中棕榈酸地塞米松和地塞米松。通过蛋白沉淀和液液萃取进行样品制备后,分析物和内标(IS)在Venusil XBP-C8柱上采用梯度洗脱进行分离。棕榈酸地塞米松、地塞米松和内标的多反应监测分别采用m/z 631.8→373.1、m/z 393.2→147.1和m/z 264.2→58.1的前体离子到产物离子的转变。该方法在棕榈酸地塞米松1.5 - 1000ng/mL和地塞米松2.5 - 250ng/mL范围内呈线性,日内和日间精密度<10%,准确度为100±7%。该测定法应用于一项涉及向健康志愿者注射棕榈酸地塞米松的临床药代动力学研究。

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