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一种用于同时测定人血浆中两种糖肽和两种小分子化合物的液相色谱-串联质谱分析法。

A LC-MS-MS assay for simultaneous determination of two glycopeptides and two small molecule compounds in human plasma.

作者信息

Shi Meiyun, Zhao Xiaojun, Wang Tingting, Yin Lei, Li Yanyan

机构信息

School of Life Science and Medicine, Dalian University of Technology, No. 2 Dagong Road, New District of Liaodong Bay, Panjin, China.

The First Hospital of Jilin University, Changchun, Jilin, China.

出版信息

J Chromatogr Sci. 2018 Oct 1;56(9):828-834. doi: 10.1093/chromsci/bmy060.

Abstract

In this study, a novel and high-throughput liquid chromatography-tandem mass spectrometric (LC-MS-MS) assay was developed and validated for simultaneous determination of two glycopeptides (vancomycin, teicoplanin) and two small molecule compounds (meropenem, voriconazole) in human plasma. Only 50 μL of human plasma is used to quantify these four drugs simultaneously at clinical concentration levels. After a relative simple protein precipitation, the supernatant was then diluted with mobile phase acetonitrile: 0.1% formic acid (5:95, v/v) to avoid solvent effect and reduce the matrix effect. Then, the target compounds were separated on an Agilent Zorbax SB-C18 column (4.6 × 50 mm, 2.7 μm). All the target compounds were detected by positive ion mode. The teicoplanin concentration was determined as the sum of six components (A2-1, A2-2, A2-3, A2-4, A2-5 and A3-1). The method was linear in the concentration range 0.3-30 μg/mL for meropenem; 1-100 μg/mL for teicoplanin and vancomycin; 0.3-10 μg/mL for voriconazole. The lower limit of quantitation (LLOQ) of meropenem and voriconazole were 0.30 μg/mL; and the LLOQ of teicoplanin and vancomycin were 1.0 μg/mL. The intra- and inter-day accuracies were <9.67% and 13.0%, and the precisions were <14.5% at all tested concentrations. The entire analysis time for the four drugs was only 5 min for each sample. The currently developed assay was successfully applied for the therapeutic drug monitoring of 85 patients administered with standard drug treatments, demonstrating its high-throughput clinical usage for the therapeutic drug monitoring.

摘要

在本研究中,开发并验证了一种新型高通量液相色谱 - 串联质谱(LC-MS-MS)分析法,用于同时测定人血浆中的两种糖肽(万古霉素、替考拉宁)和两种小分子化合物(美罗培南、伏立康唑)。仅需50μL人血浆即可在临床浓度水平同时定量这四种药物。经过相对简单的蛋白沉淀后,上清液用流动相乙腈:0.1%甲酸(5:95,v/v)稀释,以避免溶剂效应并降低基质效应。然后,目标化合物在安捷伦Zorbax SB-C18柱(4.6×50mm,2.7μm)上分离。所有目标化合物均采用正离子模式检测。替考拉宁浓度测定为六个组分(A2-1、A2-2、A2-3、A2-4、A2-5和A3-1)的总和。该方法在以下浓度范围内呈线性:美罗培南为0.3 - 30μg/mL;替考拉宁和万古霉素为1 - 100μg/mL;伏立康唑为0.3 - 10μg/mL。美罗培南和伏立康唑的定量下限(LLOQ)为0.30μg/mL;替考拉宁和万古霉素的LLOQ为1.0μg/mL。在所有测试浓度下,日内和日间准确度均<9.67%,精密度均<14.5%。每个样品中四种药物的整个分析时间仅为5分钟。目前开发的分析法已成功应用于85例接受标准药物治疗患者的治疗药物监测,证明了其在治疗药物监测中的高通量临床应用价值。

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