首页> 外文会议>223rd American Chemical Society. Meeting; 2002; Orlando, Fla. >Tetracycline and Macrolide Antibiotics Trace Analysis in Water and Wastewater Using Solid Phase Extraction and Liquid Chromatography-Tandem Mass Spectrometry
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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:固相萃取-液相色谱-串联质谱法分析水和废水中的四环素和大环内酯类抗生素

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摘要

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)提供了一种灵敏,可重现和特定的仪器方法,用于定量各种基质中的农业抗生素。通过使用固相萃取浓缩这些化合物,可以提高灵敏度并最大程度地减少干扰。聚合物萃取柱和反相萃取柱的比较表明,任一相均可提供定量结果。缓冲和/或pH调节可改善这些高极性有时有问题的化合物的回收率。在水中测定的四环素方法检测极限在0.2和0.3μg/ L之间,在缓冲废水中在1.0和2.0μg/ L之间。在缓冲水中测定的大环内酯类,林可霉素和提莫林方法的检出限为0.4至1.4μg/ L。废水中大环内酯类化合物和提莫林的检出限在1.0至3.0μg/ L之间。

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