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Flow injection chemiluminescence immunoassay for 17β-estradiol using an immunoaffinity column

机译:使用免疫亲和柱对17β-雌二醇进行流动注射化学发光免疫分析

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摘要

A new flow injection chemiluminescent immunoassay was developed for the detection of 17β-estradiol (E2). The method uses p–iodophenol (PIP) as enhancer and is based on a solid-phase immunoassay format in which an E2–OVA immobilized immunoaffinity column inserted in the flow system is used to trap unbound horseradish peroxidase (HRP)-labeled anti-E2 antibody after an off-line incubation of E2 with HRP-labeled anti-E2 antibody. The trapped enzyme conjugate was detected by injecting substrates to produce an enhanced chemiluminescence (CL) response. The linear range for E2 was 10.0–1,000.0 ng mL−1 with a correlation coefficient of 0.996 and a detection limit of 3.0 ng mL−1. The sampling and chemiluminescence detection time for one sample was 400 s after a pre-incubation procedure of 30 min. Serum samples detected by this method were in good agreement with the results obtained by EIA with E2–biotin.
机译:建立了一种新型的流动注射化学发光免疫分析法,用于检测17β-雌二醇(E2 )。该方法使用对碘苯酚(PIP)作为增强剂,并且基于固相免疫分析形式,其中使用插入流动系统中的E2 -OVA固定免疫亲和柱捕获未结合的辣根过氧化物酶(HRP)-将E2 与HRP标记的抗E2 抗体离线孵育后,可得到抗E2 抗体。通过注入底物以产生增强的化学发光(CL)反应来检测捕获的酶偶联物。 E2 的线性范围为10.0–1,000.0 ng mL-1 ,相关系数为0.996,检出限为3.0 ng mL-1 。在预孵育30分钟后,一个样品的采样和化学发光检测时间为400 s。用这种方法检测的血清样品与EIA与E2 -生物素的结果相吻合。

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