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液相色谱-串联质谱法测定人血浆中莫西沙星、环丙沙星、达托霉素、卡泊芬净和伊曲康唑的浓度。

Liquid chromatography-tandem mass spectrometry for the quantification of moxifloxacin, ciprofloxacin, daptomycin, caspofungin, and isavuconazole in human plasma.

机构信息

Institute of Clinical Microbiology and Hygiene, University Hospital Regensburg, Regensburg, Germany.

Institute of Clinical Microbiology and Hygiene, University Hospital Regensburg, Regensburg, Germany.

出版信息

J Pharm Biomed Anal. 2018 Aug 5;157:92-99. doi: 10.1016/j.jpba.2018.05.015. Epub 2018 May 12.

DOI:10.1016/j.jpba.2018.05.015
PMID:29777985
Abstract

A simple and precise ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed for the simultaneous analysis of five anti-infective agents used to treat severe infections [three antibiotics (daptomycin, moxifloxacin, ciprofloxacin) and two antifungals (isavuconazole, caspofungin)] in human plasma. Sample preparation was based on protein precipitation with ice cold methanol. All five agents were analyzed with the corresponding isotopically labeled internal standards. All analytes were detected in multiple reactions monitoring (MRM) using API 4000 triple-quadrupole mass spectrometer with electrospray (ESI) source operating in positive mode. The calibration curves were linear over the selected ranges (r > 0.99). The method is precise and accurate with a total run time of 5.5 min. Accuracy of all target analytes ranged between 95.9-116.6%, measured with an imprecision of less than 10.8%. The lower limit of quantification was 1.25 mg/L for caspofungin, 0.3125 mg/L for isavuconazole, 3.125 mg/L for daptomycin, 0.075 mg/L for ciprofloxacin, and 0.1875 mg/L for moxifloxacin. The successful application of the method in patient samples proved its suitability for the medical surveillance of antimicrobial therapy in intensive care units as well as to other pharmacokinetic studies.

摘要

建立了一种简单、准确的超高效液相色谱-串联质谱(UPLC-MS/MS)法,用于同时分析治疗严重感染的五种抗感染药物(三种抗生素[达托霉素、莫西沙星、环丙沙星]和两种抗真菌药[伊曲康唑、卡泊芬净])在人血浆中的浓度。样品制备基于用冰冷甲醇进行蛋白质沉淀。所有五种药物均采用相应的同位素标记内标进行分析。所有分析物均在 API 4000 三重四极杆质谱仪上以正模式的电喷雾(ESI)源进行多重反应监测(MRM)进行检测。校准曲线在选定范围内呈线性(r > 0.99)。该方法具有总运行时间为 5.5 分钟,精度和准确度高。所有目标分析物的准确度均在 95.9-116.6%之间,精密度小于 10.8%。卡泊芬净的定量下限为 1.25mg/L,伊曲康唑为 0.3125mg/L,达托霉素为 3.125mg/L,环丙沙星为 0.075mg/L,莫西沙星为 0.1875mg/L。该方法在患者样本中的成功应用证明了其适合于重症监护病房中抗菌治疗的医学监测以及其他药代动力学研究。

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