共 39 条
Determination of fluoroquinolones in foods using ionic liquid modified Fe3O4/MWCNTs as the adsorbent for magnetic solid phase extraction coupled with HPLC
被引:22
作者:

Zhang, Meng
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机构:
Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China

Chen, Jie
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h-index: 0
机构:
Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
Huibei Univ, Dept Food Engn, ZhiXing Coll, Wuhan 430011, Peoples R China Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China

Zhao, Faqiong
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Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China

Zeng, Baizhao
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h-index: 0
机构:
Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
机构:
[1] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
[2] Huibei Univ, Dept Food Engn, ZhiXing Coll, Wuhan 430011, Peoples R China
基金:
中国国家自然科学基金;
关键词:
POLYCYCLIC AROMATIC-HYDROCARBONS;
CARBON NANOTUBES;
SELECTIVE EXTRACTION;
COMPOSITES;
MICROEXTRACTION;
NANOCOMPOSITE;
FABRICATION;
SAMPLES;
CHICKEN;
MILK;
D O I:
10.1039/d0ay01045f
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
In this work, a simple and sensitive method based on Fe3O4/multi-walled carbon nanotubes/ionic liquid (Fe3O4/MWCNTs/IL) as the adsorbent for magnetic solid phase extraction coupled with high performance liquid chromatography was developed for the determination of trace fluoroquinolones in foods. After a simple one-pot solvothermal synthesis, Fe3O4/MWCNTs were further modified with an amine-terminated ionic liquid to enhance their dispersibility and extraction capacity. The morphology, structure and magnetic properties of the composite adsorbent were characterized by transmission electron microscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction spectrometry and vibrating-sample magnetometry. Under the optimized extraction and detection conditions, the studied fluoroquinolones were enriched effectively and separated well and their UV signals were linear to their concentrations in the range of 4-1000 ng mL(-1), with correlation coefficients ranging from 0.9958 to 0.9990. The enrichment factors were 29.1-43.9 fold and the limits of detection were 0.33-0.78 ng mL(-1). The spiked recoveries were 85.4-105.9% for milk and 85.2-103.7% for pork samples, with relative standard deviations of 0.8-5.7%. The developed method provided a fast, sensitive and reliable determination platform for fluoroquinolones in complex real samples.
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收藏
页码:4457 / 4465
页数:9
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