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首页> 外文期刊>Analytical and Bioanalytical Chemistry >Development of a monoclonal antibody-based, congener-specific and solvent-tolerable direct enzyme-linked immunosorbent assay for the detection of 2,2′,4,4′-tetrabromodiphenyl ether in environmental samples
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Development of a monoclonal antibody-based, congener-specific and solvent-tolerable direct enzyme-linked immunosorbent assay for the detection of 2,2′,4,4′-tetrabromodiphenyl ether in environmental samples

机译:基于单克隆抗体,同类物特异性和溶剂耐受的直接酶联免疫吸附测定方法的开发,用于检测环境样品中的2,2',4,4'-四溴二苯醚

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摘要

A sensitive direct enzyme-linked immunosorbent assay (ELISA) for the specific detection of 2,2′,4,4′-tetrabromodiphenyl ether (BDE-47) in environmental samples was developed. A hapten mimicking BDE-47 was synthesized by introducing a butyric acid spacer into 5-hydroxy-BDE-47 and coupled to keyhole limpet hemocyanin to form an immunogen for the production of monoclonal antibodies (Mabs) against BDE-47. The most sensitive direct ELISA was formatted with a Mab, designated as 4F2, in combination with 5-(2,4-dibromophenoxy)pentanoic acid peroxidase as a tracer. The inhibition half-maximum concentrations and limit of detection of BDE-47 in phosphate buffered saline with 25% DMSO were 1.4 ± 0.05 and 0.1 ng mL−1, respectively. Cross-reactivity values of the ELISA with the tested BDE congeners and metabolites were ≤5.8%. This assay was used to determine BDE-47 in soil, sediment and house dust samples after ultrasonic extraction, simple cleanup and concentration steps. The average recoveries, repeatabilities (intraday extractions and analyses), and intra-laboratory reproducibilities (interday extractions and analyses) were in a range of 92–126%, 8–19% and 9–25%, respectively. Applied to 44 real samples, the results of this assay displayed a statistically significant correlation with those of a gas chromatography–mass spectrometry method (R 2 = 0.79-0.85), indicating this ELISA is a suitable tool for environmental analyses of BDE-47.
机译:开发了一种灵敏的直接酶联免疫吸附试验(ELISA),用于特异性检测环境样品中的2,2',4,4'-四溴二苯醚(BDE-47)。通过将丁酸间隔基引入5-羟基-BDE-47中并与匙孔血蓝蛋白偶联形成免疫原,以生产针对BDE-47的单克隆抗体(Mabs),从而合成出模仿BDE-47的半抗原。用标记为4F2的Mab结合5-(2,4-二溴苯氧基)戊酸过氧化物酶作为示踪剂对最敏感的直接ELISA进行格式化。在含25%DMSO的磷酸盐缓冲液中,BDE-47的抑制半数最高浓度和检测极限分别为1.4±0.05和0.1 ng mL -1 。 ELISA与测试的BDE同系物和代谢物的交叉反应值为≤5.8%。超声提取,简单的清洁和浓缩步骤后,该测定用于测定土壤,沉积物和房屋灰尘样品中的BDE-47。平均回收率,重复性(日内提取和分析)和实验室内重复性(日间提取和分析)分别在92–126%,8–19%和9–25%的范围内。应用于44个真实样品,该测定结果与气相色谱-质谱法(R 2 = 0.79-0.85)的结果具有统计学意义的相关性,表明该ELISA是一种适用于BDE-47的环境分析。

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