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采用超高效液相色谱-串联质谱法同时测定重症监护病房中 11 种抗生素的浓度。

Simultaneous Measurement of 11 Antibiotics for Use in the Intensive Care Unit by Ultra-High Performance Liquid Chromatography-Tandem Mass Spectrometry.

机构信息

Department of Clinical Microbiology, Kalmar County Hospital, Kalmar.

Department of Medicine and Optometry, Linnaeus University, Kalmar.

出版信息

Ther Drug Monit. 2022 Apr 1;44(2):308-318. doi: 10.1097/FTD.0000000000000911.

Abstract

BACKGROUND

Recent studies indicate that a high proportion of patients in the intensive care unit fail to attain adequate antibiotic levels. Thus, there is a need to monitor the antibiotic concentration to ensure effective treatment. In this article, the authors aimed to develop an ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method for the simultaneous quantification of antimicrobials to assess individualized therapeutic drug monitoring.

METHODS

A UHPLC-MS/MS method with 11 antibiotics (ciprofloxacin, moxifloxacin, benzylpenicillin, levofloxacin, linezolid, rifampicin, meropenem, cloxacillin, cefotaxime, clindamycin, and piperacillin) was developed. Chromatographic separation was performed using a Kinetex Biphenyl reversed-phase column, with gradient elution using 0.1% formic acid and methanol with 0.1% formic acid. Sample preparation was performed using methanol protein precipitation. The total run time was 5 minutes.

RESULTS

For all analytes, the interassay inaccuracies for calibrators were ≤5%. The interday inaccuracies for the quality controls (QCs) were ≤5% for all analytes. The interassay precision for calibration standards ranged between 1.42% and 6.11%. The interassay imprecision for QCs of all antibiotics and concentrations ranged between 3.60% and 16.1%. Interassay inaccuracy and imprecision for the QCs and calibration standards were ≤15% for all drugs, except benzylpenicillin.

CONCLUSIONS

A rapid UHPLC-MS/MS method was developed for the simultaneous quantification of 11 different antibiotics. Minimal sample preparation was required to ensure a rapid turnaround time. The method was applied to clinical samples collected from 4 intensive care units.

摘要

背景

最近的研究表明,重症监护病房的很大一部分患者未能达到足够的抗生素水平。因此,需要监测抗生素浓度以确保有效治疗。在本文中,作者旨在开发一种超高效液相色谱-串联质谱(UHPLC-MS/MS)方法,同时定量分析抗生素,以评估个体化治疗药物监测。

方法

建立了一种同时定量分析 11 种抗生素(环丙沙星、莫西沙星、苄青霉素、左氧氟沙星、利奈唑胺、利福平、美罗培南、氯唑西林、头孢噻肟、克林霉素和哌拉西林)的 UHPLC-MS/MS 方法。采用 Kinetex Biphenyl 反相色谱柱,以 0.1%甲酸和甲醇(含 0.1%甲酸)进行梯度洗脱,采用甲醇蛋白沉淀法进行样品制备。总运行时间为 5 分钟。

结果

对于所有分析物,校准器的批间不准确度均≤5%。所有分析物的日内 QC 不准确度均≤5%。校准标准的批间精密度在 1.42%至 6.11%之间。所有抗生素和浓度 QC 的批间精密度在 3.60%至 16.1%之间。除苄青霉素外,所有药物的 QC 和校准标准的批间不准确度和不精密度均≤15%。

结论

建立了一种快速 UHPLC-MS/MS 方法,可同时定量分析 11 种不同的抗生素。该方法需要最少的样品制备,以确保快速周转时间。该方法应用于从 4 个重症监护病房采集的临床样本。

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