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

被引:20
作者
Song, Xuqin [1 ]
Zhou, Tong [2 ]
Li, Jiufeng [1 ]
Zhang, Meiyu [1 ]
Xie, Jingmeng [2 ]
He, Limin [1 ,2 ]
机构
[1] South China Agr Univ, Coll Vet Med, Natl Reference Lab Vet Drug Residues SCAU, Guangzhou 510642, Guangdong, Peoples R China
[2] South China Agr Univ, Guangdong Prov Key Lab Vet Pharmaceut Dev & Safet, Guangzhou 510642, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
molecularly imprinted polymer; macrolide drugs; solid-phase extraction; liquid chromatography-tandem mass spectrometry; water; WASTE-WATER; ANTIBIOTIC-RESISTANCE; MULTICLASS METHOD; SAMPLES; RESIDUES; POLYMERS; SURFACE; TILMICOSIN;
D O I
10.3390/molecules23051172
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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.
引用
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页数:13
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