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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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