Determination of trace fluoroquinolones in honey and milk based on cyclodextrin modified magnetic metal-organic frameworks solid phase extraction coupled with ultra-high performance liquid chromatography

被引:15
作者
Sun, Yangkun [1 ]
Kuang, Jingjing [1 ]
Cheng, Yongzhe [1 ]
Lin, Chuhui [1 ]
Zhang, Hongyang [1 ]
Zhang, Min [2 ]
Ning, Fanghong [3 ]
Hu, Ping [1 ]
机构
[1] East China Univ Sci & Technol, Sch Chem & Mol Engn, Shanghai Key Lab Funct Mat Chem, Shanghai 200237, Peoples R China
[2] East China Univ Sci & Technol, Shanghai Frontiers Sci Ctr Optogenet Tech Cell Met, Sch Pharm, Shanghai 200237, Peoples R China
[3] East China Univ Sci & Technol, Sch Biotechnol, Shanghai 200237, Peoples R China
关键词
Fluoroquinolone; Magnetic solid phase extraction; Ultra-high performance liquid chromatography; MOLECULARLY IMPRINTED POLYMERS; WATER; SAMPLES;
D O I
10.1016/j.chroma.2023.464521
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Long-term intake of animal-derived foods with excessive fluoroquinolones (FQs) will cause damage to human health, so it is critical to establish a feasible approach for sensitive and rapid monitoring of FQs residues. In this study, a new cyclodextrin modified magnetic metal-organic frameworks (Fe3O4@UiO-66-CD) was successfully synthesized by amidation reaction and applied to magnetic solid phase extraction (MSPE) for FQs analysis. The adsorption behavior of Fe3O4@UiO-66-CD was consistent with the pseudo-second-order kinetics and Freundlich isothermal adsorption model, which indicated that the designed material had various interactions on FQs, such as host-guest interaction and 7C-7C interaction. The parameters of MSPE were optimized and the determination method of norfloxacin, enrofloxacin, lomefloxacin and gatifloxacin was established by using MSPE combined with ultra-high performance liquid chromatography (UHPLC) and fluorescence detector (FLD). The method validation results displayed that the detection limits were 0.02-0.09 ng/mL, and the RSDs of intra-day and inter -day precision were less than 4.1 and 6.4 %, respectively. In the target FQs analysis of real honey and milk samples, the recoveries at different fortified concentrations were in the ranges of 88.4 % to 108.6 % with RSD <= 5.7 %. The results showed that the proposed method was sensitive, accurate and reliable for the determination of trace FQs in animal-derived foods.
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页数:9
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