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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Development of a monoclonal antibody-based indirect competitive enzyme-linked immunosorbent assay for nitroimidazoles in edible animal tissues and feeds
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Development of a monoclonal antibody-based indirect competitive enzyme-linked immunosorbent assay for nitroimidazoles in edible animal tissues and feeds

机译:基于单克隆抗体的间接竞争性酶联免疫吸附测定法在食用动物组织和饲料中硝基咪唑的开发

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摘要

The misuse of nitroimidazoles (NDZs) can lead to NDZs residues in edible animal tissues, which would be harmful to consumer health. To quickly monitor NDZs residues in edible animal tissues and feed, a monoclonal antibody-based indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) with a simple sample preparation method and clean-up was developed in the present study. At first, a broad specificity monoclonal antibody, 1D5, against NDZs has been produced, which the IC50 values of the NDZs, dimetridazole, ipronidazole, ronidazole hydroxydimetridazole, and hydroxyipronidazole, were 4.79 mu g L-1, 0.47 mu g L-1, 5.97 mu g L-1, 23.48 mu g L-1, and 15.03 mu g L-1, respectively. The limit of detection of the method for the NDZ matrix calibration ranged from 4.2 mu g kg(-1) to 50.3 mu g kg(-1) in the feed matrices and from 0.11 mu g kg(-1) to 4.11 mu g kg(-1) in the edible animal tissues matrices. The recoveries of the NDZs were in the range of 75.5-111.8%. The CVs were less than 14.4%. A good correlation (r=0.9905) between the ELISA and HPLC-MS results of the tissues demonstrated the reliability of the developed ic-ELISA, which makes it a useful tool for screening of NDZs in animal edible tissue and feed. (C) 2015 Elsevier B.V. All rights reserved.
机译:硝基咪唑(NDZs)的滥用会导致NDZs在食用动物组织中的残留,这对消费者健康有害。为了快速监测可食用动物组织和饲料中的NDZ残留,本研究开发了一种基于单克隆抗体的间接竞争酶联免疫吸附测定(ic-ELISA),该方法具有简单的样品制备方法和净化方法。首先,已生产出针对NDZ的广泛特异性单克隆抗体1D5,其NDZ,二甲达唑,ipronidazole,ronidazole hydroxydimetridazole和hydroxyipronidazole的IC50值分别为4.79μg L-1、0.47μgL-1,分别为5.97微克L-1、23.48微克L-1和15.03微克L-1。饲料基质中NDZ基质校准方法的检测限为4.2μg kg(-1)至50.3μg kg(-1)和0.11μgkg(-1)至4.11μgkg (-1)在食用动物组织基质中。 NDZ的回收率在75.5-111.8%之间。简历低于14.4%。组织的ELISA和HPLC-MS结果之间的良好相关性(r = 0.9905)证明了开发的ic-ELISA的可靠性,这使其成为筛选动物可食用组织和饲料中NDZ的有用工具。 (C)2015 Elsevier B.V.保留所有权利。

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