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Development of a real-time immuno-PCR assay for the quantification of 17β-estradiol in water

机译:实时免疫-PCR检测方法开发,用于定量水中的17β-雌二醇

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A competitive real-time (RT) immuno-polymerase chain reaction (iPCR) (RT-iPCR) assay was developed for the sensitive quantification of 17β-estradiol in water. Using a universal iPCR method and polyclonal antibodies, 17~(-1)-estradiol was accurately quantified at concentrations ranging from 1 pg mL~(-1) to 10 μg mL~(-1). The RT-iPCR assay's limit of detection was 0.7 pg mL~(-1). The RT-iPCR assay provided an 800-fold increase in sensitivity as well as an expanded working range compared with the corresponding enzyme-linked immunosorbent assay. Assay cross-reactivity to estrone and estriol, two structurally related estrogens, was below 8%. Water samples spiked with 17β-estradiol were analyzed by RT-iPCR to determine the assay's potential as a rapid screen for the monitoring of manure-borne estrogens in the environment. The assay showed recoveries of 82, 102 and 103% for Milli-Q, tap, and irrigation water, respectively, without requiring sample extraction or concentration prior to analysis.
机译:开发了一种竞争性实时(RT)免疫聚合酶链反应(iPCR)(RT-iPCR)分析方法,用于水中17β-雌二醇的灵敏定量。使用通用iPCR方法和多克隆抗体,可以在1 pg mL〜(-1)至10μgmL〜(-1)的浓度范围内准确定量17〜(-1)-雌二醇。 RT-iPCR检测的检出限为0.7 pg mL〜(-1)。与相应的酶联免疫吸附测定相比,RT-iPCR测定的灵敏度提高了800倍,工作范围扩大了。与两种结构相关的雌激素雌酮和雌三醇的交叉反应性低于8%。通过RT-iPCR分析加标有17β-雌二醇的水样品,以确定测定的潜力,可作为监测环境中粪便传播的雌激素的快速筛选。该分析表明,对于Milli-Q,自来水和灌溉用水,回收率分别为82%,102%和103%,而无需在分析前进行样品提取或浓缩。

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