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Multidetermination of Four Nitrofurans in Animal Feeds by a Sensitive and Simple Enzyme-Linked Immunosorbent Assay

机译:灵敏和简单的酶联免疫吸附法测定动物饲料中的四种硝基呋喃

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In this study,the polyclonal antibody against furazolidone was produced with furazolidone coupling to protein carriers by a diazotization method and glutaraldehyde reaction,respectively.The antibody obtained showed good specificity toward furazolidone and various cross-reactivity toward nitrofurantoin,nitrofura-zone,and furaltadone.Then,an indirect competitive enzyme-linked immunosorbent assay(ELISA)based on the antibody was first developed for multidetermination of four nitrofurans in animal feeds.The limit of detection(LOD)of the method was 0.2-2.1 ng/g depending on the component.After simple extraction,the fortified swine and broiler chicken feed samples were detected with recovery ranges of 75.9-86.4%.Results obtained from ELISA were confirmed by high-performance liquid chromatography(HPLC)with ultraviolet detection.Analysis of the unknown feed samples indicates that ELISA can be a practical tool for screening of nitrofurans in animal feeds before confirmation by HPLC.
机译:本研究通过重氮化法和戊二醛反应,将呋喃唑酮与蛋白质载体偶联,制备了抗呋喃唑酮的多克隆抗体。所得抗体对呋喃唑酮具有良好的特异性,对呋喃妥因,硝基呋喃区和呋喃他酮具有多种交叉反应性。然后,首先建立了基于抗体的间接竞争酶联免疫吸附试验(ELISA),用于动物饲料中4种硝基呋喃的多测定。该方法的检测限(LOD)为0.2-2.1 ng / g(取决于组分)简单提取后,检测到强化的猪和肉鸡饲料样品,回收率为75.9-86.4%.ELISA的结果通过高效液相色谱(HPLC)和紫外线检测得到证实。未知饲料样品的分析表明ELISA在通过HPLC确认之前可以作为筛选动物饲料中硝基呋喃的实用工具。

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