Yang Zhanjun, Fu Zhifeng, Yan Feng, Liu Hong, Ju Huangxian
Key Laboratory of Analytical Chemistry for Life Science (Ministry of Education of China), Department of Chemistry, Nanjing University, Nanjing, PR China.
Biosens Bioelectron. 2008 Sep 15;24(1):35-40. doi: 10.1016/j.bios.2008.03.007. Epub 2008 Mar 18.
A novel immunoaffinity column used as an immunosensor for flow-injection chemiluminescent (CL) immunoassay was prepared by immobilizing antibody on carboxylic resin beads. The immunosensor could fast recognize and trap the immunocomplex of horseradish peroxidase (HRP)-labeled antibody and antigen, which was firstly formed with a micro-bubble accelerated pre-incubation process, to produce a sandwich immunocomplex. The HRP introduced in the immunoaffinity column could catalyze the CL reaction to produce enzyme-enhanced emission. With alpha-fetoprotein (AFP) as a mode, a flow-injection CL immunoassay was proposed. The whole assay for one sample, including the pre-incubation and the regeneration of immunoaffinity column, could be performed within 16 min. The linear range was 1.0-80 ng/ml with a correlation coefficient of 0.998 and a detection limit of 0.1 ng/ml at a signal/noise ratio of 3. The intra- and inter-assay coefficients of variation at 20 ng/ml AFP were 1.2% and 8.5%, respectively. The storage stability of the immunoaffinity column and the accuracy for sample detection were acceptable. This flexible, sensitive, low-cost, and rapid method is valuable for clinical immunoassay.
通过将抗体固定在羧基树脂珠上,制备了一种新型免疫亲和柱,用作流动注射化学发光(CL)免疫分析的免疫传感器。该免疫传感器能够快速识别并捕获辣根过氧化物酶(HRP)标记抗体与抗原的免疫复合物,该复合物首先通过微泡加速预孵育过程形成,以产生夹心免疫复合物。免疫亲和柱中引入的HRP可催化CL反应产生酶增强发射。以甲胎蛋白(AFP)为模型,提出了一种流动注射CL免疫分析方法。对一个样品的整个分析,包括免疫亲和柱的预孵育和再生,可在16分钟内完成。线性范围为1.0 - 80 ng/ml,相关系数为0.998,在信噪比为3时检测限为0.1 ng/ml。在20 ng/ml AFP时,批内和批间变异系数分别为1.2%和8.5%。免疫亲和柱的储存稳定性和样品检测准确性均可接受。这种灵活、灵敏、低成本且快速的方法对临床免疫分析具有重要价值。