首页> 外文期刊>Journal of Agricultural and Food Chemistry >Development of a Highly Sensitive Direct Competitive Fluorescence Enzyme Immunoassay Based on a Nanobody-Alkaline Phosphatase Fusion Protein for Detection of 3-Phenoxybenzoic Acid in Urine
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Development of a Highly Sensitive Direct Competitive Fluorescence Enzyme Immunoassay Based on a Nanobody-Alkaline Phosphatase Fusion Protein for Detection of 3-Phenoxybenzoic Acid in Urine

机译:基于纳米体 - 碱性磷酸酶融合蛋白的高敏感直接竞争荧光酶免疫测定的研制,用于检测尿液3-苯氧基苯甲酸

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摘要

3-Phenoxybenzoic acid (3-PBA) is a human urinary metabolite of many pyrethroid insecticides and can be used as a biomarker to monitor human exposure to these pesticides. A rapid and sensitive direct competitive fluorescence enzyme immunoassay (dc-FEIA) for detecting 3-PBA on the basis of a nanobody (Nb)-alkaline phosphatase (AP) fusion protein was developed. The anti-3-PBA Nb-AP fusion protein was expressed and purified. The 50% inhibitory concentration (IC50) and linear range of dc-FEIA were 0.082 and 0.015-0.447 ng/mL, respectively, with a detection limit of 0.011 ng/mL. The IC50 of dc-FEIA was improved by nearly ten times compared with those of one-step and three-step direct competitive enzyme-linked immunosorbent assay (dc-ELISA). Spiked urine samples were detected by both dc-FEIA and liquid chromatography mass spectrometry (LC-MS), and the results showed good consistency between the two analysis methods, indicating the reliability of dc-FEIA based on the Nb-AP fusion protein for detecting 3-PBA in urine.
机译:3-苯氧基苯甲酸(3-PBA)是许多拟除虫菊酯杀虫剂的人尿代谢物,可用作培养物,以监测对这些农药的人体暴露。开发了一种快速敏感的直接竞争荧光酶免疫测定(DC-FEIA),用于在纳米甲型(Nb) - 甘氨酸磷酸酶(AP)融合蛋白的基础上检测3-PBA。表达并纯化抗3-PBA NB-AP融合蛋白。 DC-FeIa的50%抑制浓度(IC 50)和线性范围分别为0.082和0.015-0.447ng / ml,检测限为0.011ng / ml。与单步和三步直接竞争性酶联免疫吸附试验(DC-ELISA)相比,DC-Feia的IC50改善了近十倍。通过DC-FEIA和液相色谱质谱(LC-MS)检测掺入尿液样品,结果表明两种分析方法之间的良好一致性,表明基于NB-AP融合蛋白的DC-FEIA的可靠性进行检测尿液3-PBA。

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