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Simultaneous Analysis of Multiple Classes of Antibiotics by Ion Trap LC/MS/MS for Assessing Surface Water and Groundwater Contamination

机译:离子阱LC / MS / MS同时分析多种抗生素以评估地表水和地下水的污染

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Solid-phase extraction (SPE) and liquid chromatography in combination with ion trap mass spectrometry (LC/MS/MS) conditions were optimized for the simultaneous analysis of 13 antibiotics belonging to multiple classes and caffeine in 3 different water matrixes. The single-cartridge extraction step was developed using a reversed-phase cartridge, resulting in recoveries for the 14 compounds ranging from 71 to 119% with relative standard deviations of 16% or lower. The analytes were separated in one chromatographic run, and the SPE-LC/MS/MS detection limits ranged from 0.03 to 0.19 μg/L. The SPE procedure was validated in groundwater, surface water, and waste-water. The analysis of samples from each of the three water matrixes revealed clindamycin (1.1 μg/L) in surface water and multiple antibiotics in wastewater (0.10-1.3 μg/L). The use of identification points to unambiguously assign the identity of antibiotics in various water matrixes was applied to an ion trap data-dependent scanning method, which simultaneously collects full scan and full scan MS/MS data for the unequivocal identification of target analytes.
机译:优化了固相萃取(SPE)和液相色谱与离子阱质谱(LC / MS / MS)相结合的条件,可同时分析3种不同水基质中的13种多类抗生素和咖啡因。使用反相色谱柱开发了单墨盒萃取步骤,导致14种化合物的回收率在71%至119%之间,相对标准偏差为16%或更低。一次色谱分离分离出分析物,SPE-LC / MS / MS的检出限为0.03至0.19μg/ L。在地下水,地表水和废水中对SPE程序进行了验证。对三种水基质的样品进行的分析表明,地表水中的克林霉素(1.1μg/ L)和废水中的多种抗生素(0.10-1.3μg/ L)。使用识别点明确分配各种水基质中的抗生素的身份已应用于离子阱数据依赖性扫描方法,该方法同时收集全扫描和全扫描MS / MS数据,以明确鉴定目标分析物。

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