佩内多林
色谱法
三级四极质谱仪
分析物
美罗培南
化学
质谱法
检出限
亚胺培南
电喷雾电离
醋酸
选择性反应监测
串联质谱法
抗生素
生物化学
抗生素耐药性
作者
Chengfei Wang,Xiaowei Li,Ziquan Lv,Yingyu Wang,Yuebin Ke,Xi Xia
标识
DOI:10.1002/jssc.201901343
摘要
Abstract A rapid and reliable method for the detection of five carbapenems (biapenem, imipenem, doripenem, meropenem, and faropenem) in water was developed and validated. After acidification of water samples with acetic acid, carbapenems were isolated using a Bond Elut PPL cartridge. The target compounds were separated using ultra high performance liquid chromatography with a chromatographic run time of 5 min and detected on a triple quadrupole mass spectrometer operated in positive electrospray ionization and multiple reaction monitoring mode. Mean recoveries were in the range of 76.6–106.5%, with satisfactory intraday and interday relative standard deviations lower than 10.0 and 10.8%, respectively. The limits of detection and quantification were in the ranges of 0.05–0.2 µg/L and 0.1–0.5 µg/L, respectively, depending on the analyte. The proposed method was applied to the analysis of river samples and wastewater samples from swine farms, and no carbapenems were detected in the collected samples.
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