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使用超高效液相色谱-串联质谱法对人血浆中的β-内酰胺类抗生素进行超快速定量分析。

Ultrafast quantification of β-lactam antibiotics in human plasma using UPLC-MS/MS.

作者信息

Carlier Mieke, Stove Veronique, De Waele Jan J, Verstraete Alain G

机构信息

Department of Clinical Chemistry, Microbiology and Immunology, Ghent University, De Pintelaan 185, Building 2P8, 9000 Ghent, Belgium; Department of Critical Care Medicine, Ghent University, De Pintelaan 185, Building 2K12-IC, 9000 Ghent, Belgium.

Department of Clinical Chemistry, Microbiology and Immunology, Ghent University, De Pintelaan 185, Building 2P8, 9000 Ghent, Belgium; Department of Laboratory Medicine, Ghent University Hospital, De Pintelaan 185, Building 2P8, 9000 Ghent, Belgium.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2015 Jan 26;978-979:89-94. doi: 10.1016/j.jchromb.2014.11.034. Epub 2014 Dec 8.

Abstract

There is an increasing interest in monitoring plasma concentrations of β-lactam antibiotics. The objective of this work was to develop and validate a fast ultra-performance liquid chromatographic method with tandem mass spectrometric detection (UPLC-MS/MS) for simultaneous quantification of amoxicillin, cefuroxime, ceftazidime, meropenem and piperacillin with minimal turn around time. Sample clean-up included protein precipitation with acetonitrile containing 5 deuterated internal standards, and subsequent dilution of the supernatant with water after centrifugation. Runtime was only 2.5 min. Chromatographic separation was performed on a Waters Acquity UPLC system using a BEH C18 column (1.7 μm, 100 mm × 2.1 mm) applying a binary gradient elution of water and methanol both containing 0.1% formic acid and 2 mmol/L ammonium acetate on a Water TQD instrument in MRM mode. All compounds were detected in electrospray positive ion mode and could be quantified between 1 and 100 mg/L for amoxicillin and cefuroxime, between 0.5 and 80 mg/L for meropenem and ceftazidime, and between 1 and 150 mg/L for piperacillin. The method was validated in terms of precision, accuracy, linearity, matrix effect and recovery and has been compared to a previously published UPLC-MS/MS method.

摘要

监测β-内酰胺类抗生素的血浆浓度正受到越来越多的关注。本研究的目的是开发并验证一种快速超高效液相色谱-串联质谱检测法(UPLC-MS/MS),以同时定量阿莫西林、头孢呋辛、头孢他啶、美罗培南和哌拉西林,且周转时间最短。样品净化包括用含有5种氘代内标的乙腈进行蛋白沉淀,离心后用水稀释上清液。运行时间仅为2.5分钟。在Waters Acquity UPLC系统上,使用BEH C18柱(1.7μm,100mm×2.1mm)进行色谱分离,在Water TQD仪器上采用二元梯度洗脱,流动相为均含有0.1%甲酸和2mmol/L醋酸铵的水和甲醇,采用MRM模式。所有化合物均在电喷雾正离子模式下检测,阿莫西林和头孢呋辛的定量范围为1至100mg/L,美罗培南和头孢他啶为0.5至80mg/L,哌拉西林为1至150mg/L。该方法在精密度、准确度、线性、基质效应和回收率方面进行了验证,并与之前发表的UPLC-MS/MS方法进行了比较。

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