Department of Clinical Chemistry, Microbiology and Immunology, Ghent University, De Pintelaan 185, Building 2P8, 9000 Ghent, Belgium.
Int J Antimicrob Agents. 2012 Nov;40(5):416-22. doi: 10.1016/j.ijantimicag.2012.06.022. Epub 2012 Aug 10.
There is an increasing interest in monitoring plasma concentrations of β-lactam antibiotics. The objective of this work was to develop and validate a rapid ultra-performance liquid chromatographic method with tandem mass spectrometric detection (UPLC-MS/MS) for simultaneous quantification of amoxicillin, ampicillin, cefuroxime, cefazolin, ceftazidime, meropenem, piperacillin, clavulanic acid and tazobactam. Sample clean-up included protein precipitation with acetonitrile and back-extraction of acetonitrile with dichloromethane. Six deuterated β-lactam antibiotics were used as internal standards. Chromatographic separation was performed on a Waters ACQUITY UPLC system using a BEH C(18) column (1.7 μm, 100 mm×2.1 mm) applying a binary gradient elution of water and acetonitrile both containing 0.1% formic acid. The total run time was 5.5 min. The developed method was validated in terms of precision, accuracy, linearity, matrix effect and recovery. The assay has now been successfully used to determine concentrations of amoxicillin/clavulanic acid, cefuroxime and meropenem in plasma samples from intensive care patients.
人们对监测β-内酰胺类抗生素的血浆浓度越来越感兴趣。本工作旨在开发和验证一种快速的超高效液相色谱-串联质谱法(UPLC-MS/MS),用于同时定量检测阿莫西林、氨苄西林、头孢呋辛、头孢唑林、头孢他啶、美罗培南、哌拉西林、克拉维酸和他唑巴坦。样品的净化包括用乙腈进行蛋白沉淀,然后用二氯甲烷反萃取乙腈。使用 6 种氘代β-内酰胺类抗生素作为内标。色谱分离在 Waters ACQUITY UPLC 系统上进行,采用 BEH C(18)柱(1.7 μm,100 mm×2.1 mm),采用水和乙腈的二元梯度洗脱,两者均含有 0.1%甲酸。总运行时间为 5.5 分钟。该方法已在精密度、准确度、线性、基质效应和回收率方面得到验证。该测定方法现已成功用于确定重症监护患者血浆样本中阿莫西林/克拉维酸、头孢呋辛和美罗培南的浓度。