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Tetracycline and Macrolide Antibiotics Trace Analysis in Water and Wastewater Using Solid Phase Extraction and Liquid Chromatography-Tandem Mass Spectrometry

机译:使用固相萃取和液相色谱 - 串联质谱法在水和废水中的四环素和大环内德抗生素痕量分析

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Liquid chromatography-tandem mass spectrometry (LC/MS/MS) provides a sensitive, reproducible, and specific instrumental method for quantifying agricultural antibiotics in a variety of matrices. Sensitivity can be enhanced and interferences minimized by concentrating these compounds using solid phase extraction. Comparison of polymeric and reverse phase extraction cartridges suggests that either phase may provide quantitative results. Buffering and/or pH adjustment improves the recovery of these highly polar and sometimes problematic compounds. Tetracycline method detection limits determined in water are between 0.2 and 0.3 μg/L, and between 1.0 and 2.0 μg/L in buffered wastewater. Macrolides, lincomycin, and tiamulin method detection limits determined in buffered water are between 0.4 and 1.4 μg/L. Macrolides and tiamulin detection limits are between 1.0 and 3.0 μg/L in wastewater.
机译:液相色谱 - 串联质谱(LC / MS / MS)提供了用于量化各种基质的农业抗生素的敏感,可重复和特异性的仪器方法。通过使用固相萃取浓缩这些化合物,可以提高灵敏度和最小化干扰。聚合物和反相萃取盒的比较表明,任一相可以提供定量结果。缓冲和/或pH调节改善了这些高极性和有时有问题的化合物的回收。水中测定的四环素方法检测限值在缓冲废水中的0.2至0.3μg/ L之间,介于1.0至2.0μg/ L之间。在缓冲水中测定的大溴化锌,林霉素和硫蛋白方法检测限度在0.4和1.4μg/ L之间。大环内酯和硫醇素检测限度在废水中的1.0和3.0μg/ L之间。

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