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Anal Chim Acta. 2009 Oct 27;653(2):167-72. doi: 10.1016/j.aca.2009.09.024. Epub 2009 Sep 22.
2
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Talanta. 2006 Mar 15;69(1):216-25. doi: 10.1016/j.talanta.2005.09.032. Epub 2005 Oct 27.
3
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Talanta. 2006 Feb 15;68(4):1215-21. doi: 10.1016/j.talanta.2005.07.035. Epub 2005 Aug 25.
4
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An amperometric hydrogen peroxide biosensor based on immobilization of horseradish peroxidase on an electrode modified with magnetic dextran microspheres.一种基于辣根过氧化物酶固定在磁性葡聚糖微球修饰电极上的安培型过氧化氢生物传感器。
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J Agric Food Chem. 2007 Aug 22;55(17):6879-84. doi: 10.1021/jf070978g. Epub 2007 Jul 24.
7
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建立一种电化学免疫分析法用于检测猪尿液中的加替沙星。

Development of an electrochemical immunoassay for detection of gatifloxacin in swine urine.

机构信息

School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.

出版信息

J Zhejiang Univ Sci B. 2012 Feb;13(2):118-25. doi: 10.1631/jzus.B1100073.

DOI:10.1631/jzus.B1100073
PMID:22302425
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3274739/
Abstract

To detect gatifloxacin (GAT) residue in swine urine, an electrochemical immunoassay was established. An indirect competitive immunoassay was developed, in which the coating antigen is immobilized in an enzyme-linked immunosorbent assay (ELISA) plate and GAT residue from the sample competes with the limited binding sites in added anti-GAT antibody. Horseradish peroxidase (HRP) conjugated to goat anti-rabbit IgG was used as the enzymatic label. A carbon fiber working electrode was constructed and current signals were detected by using hydrogen peroxide as a substrate and hydroquinone as an electrochemical mediator. The electrochemical immunoassay was evaluated by analysis of GAT in buffer or swine urine and an average value of half inhibition concentration (IC(50)) of 8.9 ng/ml was obtained. Excellent specificity of the antibody was achieved with little cross-reaction with lomefloxacin (3.0%), ciprofloxacin (3.0%), and ofloxacin (1.9%) among commonly used (fluoro)quinolones. In conclusion, the immunoassay system developed in this research can be used as a rapid, powerful and on-site analytical tool to detect GAT residue in foods and food products.

摘要

为了检测猪尿中的加替沙星(GAT)残留,建立了电化学免疫分析方法。开发了一种间接竞争免疫分析方法,其中包被抗原固定在酶联免疫吸附测定(ELISA)板上,并且来自样品的 GAT 残留与添加的抗 GAT 抗体中的有限结合位点竞争。辣根过氧化物酶(HRP)缀合到兔抗山羊 IgG 上作为酶标记物。构建了碳纤维工作电极,并通过使用过氧化氢作为底物和对苯二酚作为电化学介体来检测电流信号。通过在缓冲液或猪尿中分析 GAT 对电化学免疫分析进行了评估,得到平均半抑制浓度(IC(50))为 8.9ng/ml。该抗体具有良好的特异性,与常用(氟)喹诺酮类药物中的洛美沙星(3.0%)、环丙沙星(3.0%)和氧氟沙星(1.9%)几乎没有交叉反应。总之,本研究开发的免疫分析系统可用于快速、强大和现场分析检测食品和食品产品中的 GAT 残留。