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中国精品科技期刊2020
龙芳. 磁性印迹固相萃取-印迹电化学传感器联用技术快速检测肉制品中的红霉素[J]. 食品工业科技,2022,43(1):269−278. doi: 10.13386/j.issn1002-0306.2021030181.
引用本文: 龙芳. 磁性印迹固相萃取-印迹电化学传感器联用技术快速检测肉制品中的红霉素[J]. 食品工业科技,2022,43(1):269−278. doi: 10.13386/j.issn1002-0306.2021030181.
LONG Fang. Magnetic Imprinted Solid-Phase Extraction Combined with Imprinted Electrochemical Sensor for Rapid Detection of Erythromycin in Meat Products[J]. Science and Technology of Food Industry, 2022, 43(1): 269−278. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2021030181.
Citation: LONG Fang. Magnetic Imprinted Solid-Phase Extraction Combined with Imprinted Electrochemical Sensor for Rapid Detection of Erythromycin in Meat Products[J]. Science and Technology of Food Industry, 2022, 43(1): 269−278. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2021030181.

磁性印迹固相萃取-印迹电化学传感器联用技术快速检测肉制品中的红霉素

Magnetic Imprinted Solid-Phase Extraction Combined with Imprinted Electrochemical Sensor for Rapid Detection of Erythromycin in Meat Products

  • 摘要: 本文旨在构建一种简便、快捷的肉制品中痕量红霉素磁性分子印迹固相萃取-印迹电化学传感器联用的分析方法。采用新型表面印迹技术,制备出对ERY具有高选择性与灵敏性的红霉素磁性分子印迹聚合物(MMIP),再分别以MMIP作为固相萃取剂及电化学传感元构建印迹固相萃取-印迹电化学传感器(MMISPE-MMIP-sensor)联用技术快速检测系统。采用循环伏安(CV)及差分脉冲伏安(DPV)等方法对其电学性能进行探讨,通过红外光谱、扫描电镜(SEM)和透射电镜(TEM)对其结构和形态进行表征。实验考察了缓冲溶液pH和孵化时间对印迹电极的影响。结果表明,最佳缓冲溶液pH为7.5,富集时间为10 min。在最优实验条件下,该印迹电极的响应电流△IR与ERY浓度的负对数(-logCERY)在1.0×10−10~1.0×10−5 mol/L范围内呈良好的线性关系,相关系数为0.991,最低检出限为1.0×10−10 mol/L。以AZI、STM、ROX三种结构类似物为干扰物,研究该印迹电极对ERY的吸附选择性。结果显示,该印迹电极只对红霉素分子具有特异识别作用而呈现最大响应值(0.72 mA)。重现性和稳定性实验结果显示该电极具有良好的重现性和稳定性。联用检测结果显示通过磁固相萃取和印迹电化学双预浓缩过程将样品中ERY富集浓度提高了9~12倍。

     

    Abstract: This paper aims to construct a simple and rapid method for analyzing trace amounts of erythromycin (ERY) in meat products by magnetic molecular imprinted solid-phase extraction combined with imprinted electrochemical sensors. Using ERY as the template molecule, dopamine (DA) as the functional monomer, and functionalized magnetic graphene-carbon nanotube composite as the modified carrier, erythromycin magnetic molecularly imprinted polymer (MMIP) with good selectivity and sensitivity to ERY was prepared by using a novel surface imprinting technology. Then, the magnetic imprinted solid-phase extraction combined with imprinted electrochemical sensor (MMISPE-MMIP-sensor) for rapid detection system was constructed by using MMIP as solid phase extraction agent and electrochemical sensor element, respectively. The methods including cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were used to discuss its electrical properties of the sensor with K3Fe (CN)6 solution, and its structure and morphology were characterized by fourier infrared spectroscopy (FTIR) and scanning electron microscope (SEM) and transmission electron microscope (TEM). The results showed that the surface of the carbon nanotube-graphene composite was covered with an imprinted polymer shell layer, and the shell layer have many nanoparticles on the surface. The effects of pH value of buffer solution and response time on the imprinted electrode were investigated. The results showed that the best buffer pH was 7.5, and the enrichment time was 10 min. Under this optimal conditions, the experimental conditions were optimized, the response current △IR and the negative logarithm (-logCERY) of ERY concentration showed a good linear relationship in the range of 1.0×10−10~1.0×10−5 mol/L, the correlation coefficient was 0.991, and the lowest detection limit was 1.0×10−10 mol/L. The selectivity experiments of ERY on the imprinted electrode were studied by using three structural analogues AZI、STM and ROX as interferers. The results showed that the imprinted electrode only had a specific recognition effect on ERY and showed a maximum response value (0.72 mA); The results of reproducibility and stability experiments suggested that the electrode had good reproducibility and stability. The detection results suggested that the concentration of ERY enrichment in the samples were increased 9~12 times by the magnetic imprinted solid-phase extraction combined with imprinted electrochemical sensor preconcentration process.

     

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