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Determination of Ten Macrolide Drugs in Environmental Water Using Molecularly Imprinted Solid-Phase Extraction Coupled with Liquid Chromatography-Tandem Mass Spectrometry

机译:分子印迹固相萃取-液相色谱-串联质谱法测定环境水中的十种大环内酯类药物

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摘要

With the extensive application of antibiotics in livestock, their contamination of the aquatic environment has received more attention. Molecularly imprinted polymer (MIP), as an eco-friendly and durable solid-phase extraction material, has shown great potential for the separation and enrichment of antibiotics in water. This study aims at developing a practical and economical method based on molecularly imprinted solid phase extraction (MISPE) combined with liquid chromatography-tandem mass spectrometry (LC-MS/MS) for simultaneously detecting ten macrolide drugs in different sources of water samples. The MIP was synthesized by bulk polymerization using tylosin as the template and methacrylic acid as the functional monomer. The MIP exhibited a favorable load-bearing capacity for water (>90 mL), which is more than triple that of non-molecularly imprinted polymers (NIP). The mean recoveries of macrolides at four spiked concentration levels (limit of quantification, 40, 100, and 400 ng/L) were 62.6–100.9%, with intra-day and inter-day relative standard deviations below 12.6%. The limit of detection and limit of quantification were 1.0–15.0 ng/L and 3.0–40.0 ng/L, respectively. Finally, the proposed method was successfully applied to the analysis of real water samples.
机译:随着抗生素在牲畜中的广泛应用,其对水生环境的污染受到了越来越多的关注。分子印迹聚合物(MIP)作为一种环保且耐用的固相萃取材料,在水中分离和富集抗生素方面显示出巨大潜力。这项研究的目的是开发一种基于分子印迹固相萃取(MISPE)结合液相色谱-串联质谱(LC-MS / MS)的实用且经济的方法,该方法可同时检测不同水样源中的十种大环内酯类药物。以泰乐菌素为模板,甲基丙烯酸为功能单体,通过本体聚合合成了MIP。 MIP对水具有良好的承重能力(> 90 mL),是非分子印迹聚合物(NIP)的三倍以上。在四个加标浓度水平(定量极限为40、100和400 ng / L)下大环内酯类化合物的平均回收率为62.6-100.9%,日内和日间相对标准偏差低于12.6%。检出限和定量限分别为1.0–15.0 ng / L和3.0–40.0 ng / L。最后,该方法成功地应用于实际水样的分析。

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