Determination of fluoroquinolones in food samples by magnetic solid-phase extraction based on a magnetic molecular sieve nanocomposite prior to high-performance liquid chromatography and tandem mass spectrometry

被引:35
作者
Yu, Hao [1 ]
Jia, Yuqian [1 ]
Wu, Ri [2 ]
Chen, Xiangfeng [1 ,2 ]
Chan, T-W Dominic [2 ]
机构
[1] Qilu Univ Technol, Shandong Anal & Test Ctr, Key Lab Appl Technol Sophisticated Analyt Instrum, Shandong Acad Sci, Jinan 250014, Shandong, Peoples R China
[2] Chinese Univ Hong Kong, Dept Chem, HICSAR, Hong Kong, Peoples R China
关键词
Fluoroquinolones; Magnetic solid-phase extraction; Food; Tandem mass spectrometry; Molecular sieve; WALLED CARBON NANOTUBES; WATER SAMPLES; CAPILLARY-ELECTROPHORESIS; SELECTIVE EXTRACTION; IMPRINTED POLYMERS; ORGANIC FRAMEWORK; QUINOLONES; MILK; REMOVAL; ANTIMICROBIALS;
D O I
10.1007/s00216-019-01726-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this study, a magnetic molecular sieve material (Fe3O4@MCM-48) was synthesized by a combination of solvothermal and self-assembly methods. The physicochemical properties of the magnetic molecular sieve material were characterized by scanning electron microscopy, energy-dispersive spectroscopy, magnetic hysteresis loop measurements, transmission electron microscopy, powder X-ray diffraction, N-2 adsorption-desorption analysis, and Fourier transform infrared spectroscopy. The as-synthesized nanocomposite showed various advantages, including easy magnetic-assisted separation, high specific surface area, and a highly interwoven and branched mesoporous structure. The Fe3O4@MCM-48 nanocomposite was then used as an effective adsorbent material for magnetic solid-phase extraction of fluoroquinolones (FQs) from water samples. The FQs in the extract were determined via liquid chromatography-tandem mass spectrometry. Adsorption and desorption factors that affected the extraction performance were systematically optimized using spiked purified water samples. Good linearity (with R-2>0.99) was shown by this FQ detection system for FQ concentrations from 5 to 1000ngL(-1). Moreover, low detection limits (0.7-6.0ngL(-1)) and quantitation limits (2.5-20.0ngL(-1)) and satisfactory repeatability (relative standard deviation <10%, n=6) were achieved for water samples. The developed method was also validated for the analysis of FQs in meat and milk samples. Finally, FQs in food and drinking water samples were successfully determined using the developed method.
引用
收藏
页码:2817 / 2826
页数:10
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