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Rapid detection of neuron specific enolase by chemiluminescence immunoassay using bio-functionlized magnetic nanocomposites

机译:使用生物功能化磁性纳米复合物的化学发光免疫分析法快速检测神经元特异性烯醇化酶

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To detect a biomarker for small cell lung carcinoma (SCLC), neuron specific enolase (NSE), a chemiluminescent immunoassay combined with immunomagnetic separation was proposed, in which bio-functionalized magnetic nanocomposites (BFMNs) were used as mobile substrate for capturing and isolating the NSE proteins. The BFMNs coated with anti-NSE antibody would connect with NSE and horseradish peroxidase labeled anti-NSE antibody in a sandwich-type detection manner. After fast magnetic collection, the sandwich immunocomplex is separated from excess antiboby or non-specific proteins. The immunocomplex further reacts with chemiluminescent substrate to produce chemiluminescence. A home-made three-channel luminometer was used to detect the chemiluminescence so as to improve the detection speed. There is a good linear response between the chemiluminescence intensity and the NSE concentration in the range from 2 to 200 ng/mL. The proposed immunoassay also shows good reproducibility and excellent selectivity for NSE against other proteins. The whole detection process including incubation, washing and detection could be performed within 40 min. The proposed method offers a simple, noninvasive and reliable tool for detecting SCLC and has potential application for clinical testing.
机译:为了检测小细胞肺癌(SCLC),神经元特异性烯醇化酶(NSE)的生物标志物,提出了一种化学发光免疫分析与免疫磁分离相结合的方法,其中以生物功能化的磁性纳米复合物(BFMNs)作为可移动的基质来捕获和分离肿瘤细胞NSE蛋白。涂有抗NSE抗体的BFMN将以夹心型检测方式与NSE和辣根过氧化物酶标记的抗NSE抗体连接。快速收集磁性后,将夹心免疫复合物与过量的抗体或非特异性蛋白分离。免疫复合物进一步与化学发光底物反应产生化学发光。采用自制的三通道发光仪检测化学发光,提高了检测速度。化学发光强度与NSE浓度之间在2到200 ng / mL的范围内具有良好的线性响应。拟议的免疫测定法还显示出针对其他蛋白质对NSE的良好重现性和出色的选择性。整个检测过程包括孵育,洗涤和检测可以在40分钟内完成。所提出的方法提供了一种简单,无创且可靠的检测SCLC的工具,并在临床测试中具有潜在的应用。

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