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首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >Magnetic bead-based phage anti-immunocomplex assay (PHAIA) for the detection of the urinary biomarker 3-phenoxybenzoic acid to assess human exposure to pyrethroid insecticides
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Magnetic bead-based phage anti-immunocomplex assay (PHAIA) for the detection of the urinary biomarker 3-phenoxybenzoic acid to assess human exposure to pyrethroid insecticides

机译:基于磁珠的噬菌体抗免疫复合物测定法(PHAIA)用于检测尿液生物标志物3-苯氧基苯甲酸以评估人体与拟除虫菊酯杀虫剂的接触

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摘要

Noncompetitive immunoassays are advantageous over competitive assays for the detection of small molecular weight compounds. We recently demonstrated that phage peptide libraries can be an excellent source of immunoreagents that facilitate the development of sandwich-type noncompetitive immunoassays for the detection of small analytes, avoiding the technical challenges of producing anti-immunocomplex antibody. in this work we explore a new format that may help to optimize the performance of the phage anti-immunocomplex assay (PHAIA) technology. As a model system we used a polyclonal antibody to 3-phenoxybenzoic acid (3-PBA) and an anti-immunocomplex phage clone bearing the cyclic peptide CFNGKDWLYC. The assay setup with the biotinylated antibody immobilized onto streptavidin-coated magnetic beads significantly reduced the amount of coating antibody giving identical sensitivity (50% saturation of the signal (SC50) = 0.2-0.4 ng/ml) to the best result obtained with direct coating of the antibody on ELISA plates. The bead-based assay tolerated LIP to 10 and 5% of methanol and urine matrix, respectively. This assay system accurately determined the level of spiked 3-PBA in different urine samples prepared by direct dilution or clean-up with solid-phase extraction after acidic hydrolysis with overall recovery of 80-120%. (c) 2009 Elsevier Inc. All rights reserved.
机译:对于检测小分子量化合物,非竞争性免疫分析优于竞争性分析。我们最近证明,噬菌体肽库可以是免疫试剂的极佳来源,可促进夹心型非竞争性免疫分析方法的发展,以检测小的分析物,从而避免了产生抗免疫复合抗体的技术挑战。在这项工作中,我们探索了一种可能有助于优化噬菌体抗免疫复合物测定(PHAIA)技术性能的新格式。作为模型系统,我们使用了针对3-苯氧基苯甲酸(3-PBA)的多克隆抗体和带有环肽CFNGKDWLYC的抗免疫复合物噬菌体克隆。将生物素化抗体固定在抗生蛋白链菌素包被的磁珠上的测定设置显着减少了包被抗体的量,从而与直接包被获得的最佳结果具有相同的灵敏度(信号的50%饱和度(SC50)= 0.2-0.4 ng / ml) ELISA板上的抗体检测。基于珠的测定法分别将LIP耐受10%和5%的甲醇和尿液基质。该测定系统可通过酸性水解后直接稀释或固相萃取净化,准确测定不同尿液样品中加标的3-PBA含量,总回收率为80-120%。 (c)2009 Elsevier Inc.保留所有权利。

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