A single antibody sandwich electrochemiluminescence immunosensor based on protein magnetic molecularly imprinted polymers mimicking capture probes

被引:52
作者
Zhou, Jing [1 ]
Gan, Ning [1 ]
Hu, Futao [2 ]
Li, Tianhua [1 ]
Zhou, Hankun [1 ]
Li, Xing [1 ]
Zheng, Lei [3 ]
机构
[1] Ningbo Univ, State Key Lab Base Novel Funct Mat & Preparat Sci, Fac Mat Sci & Chem Engn, Ningbo 315211, Zhejiang, Peoples R China
[2] Fac Marine, Ningbo 315211, Zhejiang, Peoples R China
[3] Southern Med Univ, Nanfang Hosp, Guangzhou 510515, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Single antibody sandwich; Electrochemiluminescence immunosensor; Magnetic molecularly imprinted polymers; Ru-silica (Ru(bpy)(3)(2+)-doped silica) doped; Au nanocomposites; Hemoglobin; ELECTROGENERATED CHEMILUMINESCENCE; QUANTUM DOTS; SILICA NANOPARTICLES; GOLD NANOPARTICLES; HEMOGLOBIN; ELECTRODE; BIOSENSOR; GRAPHENE; SENSITIVITY; NANODOTS;
D O I
10.1016/j.snb.2013.06.021
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A single antibody sandwich electrochemiluminescence (ECL) immunosensor for ultratrace detection of protein was developed using magnetic molecularly imprinted polymers (MMIPs) as an alternative to the first antibody as capture probes and antibodies labeled with Ru-silica (Ru(bpy)(3)(2+)-doped silica) doped Au (Ru@SiO2@Au) nanocomposites as labels. Using MMIPs as capture probes will aid mass production, greatly reduce costs and avoid the loss of bioactivity associated with the use of conventional antibodies. Moreover, MMIPs can be easily immobilized on and washed off simply by adding or removing a magnet on the electrode, which will greatly simplify the preparation and allow regeneration of the sensor. Lastly, MMIPs can enrich ultratrace levels of antigens from sample solutions to produce more immunocomplex than the conventional capture probe, thus providing an ultrasensitive assay. The logarithm of Delta ECL intensity depended linearly on the logarithm of the hemoglobin (Hb) concentration in the range from 0.1 to 4 x 10(4) pg mL(-1) with a detection limit of 0.023 pg mL(-1). This approach offers obvious advantages of low cost, high sensitivity and enhanced stability compared with other immunosensors, and therefore offers significant potential for protein detection in a clinical laboratory setting. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:300 / 307
页数:8
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