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Development and Validation of a Sensitive Indirect Competitive Enzyme-Linked Immunosorbent Assay for the Screening of Florfenicol and Thiamphenicol in Edible Animal Tissue and Feed

机译:间接间接竞争性酶联免疫吸附试验的开发和验证,用于筛选食用动物组织和饲料中的氟苯尼考和甲氧苯丙胺

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摘要

To monitor the illegal use of florfenicol (FF) and thiamphenicol (TAP) in edible animal tissue and feed, a sensitive monoclonal antibody-based indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) has been developed with simple sample preparation and cleanup. The obtained monoclonal antibody (5F4) that has isotype IgG1 showed an IC50 value of 0.21 mu g L-1 for FF and 0.35 mu g L-1 for TAP, respectively. It did not exhibit measurable cross-reactivity with other antibiotics. The limits of detection (LODs) for FF and TAP in a muscle matrix ranged from 0.07 to 0.14 mu g kg(-1) and in a feed matrix ranged from 2.9 to 5.2 mu g kg(-1). The recoveries were 72.8 to 113.4 % with a coefficient of variation of less than 15 %. Good correlation between the ELISA and HPLC-MS/MS results in the tissues tested demonstrated the reliability of our ic-ELISA. This ELISA is a useful tool for screening FF and TAP in edible animal tissue and feed.
机译:为了监测可食用动物组织和饲料中非法使用氟苯尼考(FF)和甲砜霉素(TAP),已经开发了一种基于敏感单克隆抗体的间接竞争酶联免疫吸附测定(ic-ELISA),其样品制备和净化简单。获得的具有同种型IgG1的单克隆抗体(5F4)对FF的IC50值分别为0.21μgL-1和对TAP的IC50值为0.35μgL-1。它与其他抗生素没有可测量的交叉反应性。 FF和TAP在肌肉基质中的检测限(LODs)为0.07至0.14μg kg(-1),在饲料基质中为2.9至5.2μg kg(-1)。回收率为72.8至113.4%,变异系数小于15%。 ELISA和HPLC-MS / MS结果在组织中的良好相关性证明了我们ic-ELISA的可靠性。此ELISA是筛选食用动物组织和饲料中FF和TAP的有用工具。

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