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Abstract: 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
Template and target information: tylosin, macrolide drugs, tilmicosin, TIL, erythromycin, ERY, kitasamycin, KIT, roxithromycin, ROX, josamycin, JOS, spiramycin, SPM, azithromycin, AZI, clarithromycin, CLA, midecamycin, MED, tulathromycin, TUL
Author keywords: molecularly imprinted polymer, Macrolide drugs, Solid-phase extraction, Liquid chromatography-tandem mass spectrometry, water