分子印迹聚合物选择性提取动物源性食品中氧化苯达唑残留的研究。

IF 2.8 3区 工程技术 Q2 CHEMISTRY, ANALYTICAL
Yue Qiu, Yue Wang, Chengli Xie, Yike Huang, Genrong Li, Zhining Xia
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引用次数: 0

摘要

为实现难溶兽药氧苯达唑的特异性吸附制样,本研究以4-乙烯基吡啶为功能单体,在功能化二氧化硅纳米颗粒表面进行自由基聚合,合成表面分子印迹聚合物(OBZMIP)。该OBZMIP在30 min内对氧苯并唑具有良好的吸附能力,其吸附行为符合拟二级动力学模型和Langmuir模型,最大吸附量为4.93 mg/g。经过5次吸附-解吸循环后,吸附量保持不变,具有良好的重复使用性能。在含有8种相似化合物的混合体系中,选择性系数在1.3 ~ 16.9之间,具有较强的特异性识别能力。作为固相萃取的吸附填料,制备的OBZMIP对四种不同肉类样品的氧苯并唑提取率均有显著提高。因此,OBZMIP在肉类样品预处理过程中兽药氧苯达唑残留的选择性提取中具有广阔的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Research on the Selective Extraction of Oxibendazole Residues in Animal-Derived Food Using Molecularly Imprinted Polymers

To achieve specific adsorption-based sample preparation for the poorly soluble veterinary drug oxibendazole, this study employed 4-vinylpyridine as the functional monomer and conducted radical polymerization on the surface of functionalized silica nanoparticles to synthesize a surface molecularly imprinted polymer (OBZMIP). This OBZMIP exhibited good adsorption capacity for oxibendazole within 30 min, with its adsorption behavior conforming to the pseudo–second-order kinetic and Langmuir models, predicting a maximum adsorption capacity of 4.93 mg/g. After five adsorption–desorption cycles, the adsorption capacity remained unchanged, demonstrating excellent reusability. In a mixed system containing eight similar compounds, the selectivity coefficients ranged from 1.3 to 16.9, indicating outstanding specific recognition ability. Utilized as an adsorbent packing material for solid-phase extraction, the prepared OBZMIP demonstrated significantly high recovery rates in the extraction of oxibendazole from four distinct meat samples. Therefore, OBZMIP holds promising applications in the selective extraction of veterinary drug oxibendazole residues during the pretreatment of meat samples.

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来源期刊
Journal of separation science
Journal of separation science 化学-分析化学
CiteScore
6.30
自引率
16.10%
发文量
408
审稿时长
1.8 months
期刊介绍: The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.
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