Chemiluminescence enzyme immunoassay using magnetic nanoparticles for detection of neuron specific enolase in human serum

被引:47
作者
Fu, Xiaoling [3 ,4 ]
Meng, Meng [1 ,2 ]
Zhang, Yu [1 ,2 ]
Yin, Yongmei [1 ,2 ]
Zhang, Xiangsheng [3 ]
Xi, Rimo [1 ,2 ]
机构
[1] Coll Pharm, State Key Lab Med Chem Biol, Tianjin 300071, Peoples R China
[2] Tianjin Key Lab Mol Drug Res, Tianjin 300071, Peoples R China
[3] Cent S Univ, Xiangya Hosp 2, Dept Orthopaed, Changsha 410011, Hunan, Peoples R China
[4] Nanchang Univ, Affiliated Hosp 2, Dept Orthopaed, Nanchang 330000, Peoples R China
关键词
Magnetic particle separation; Chemiluminescence enzyme immunoassay; Neuron specific enolase (NSE); Small cell lung carcinoma (SCLC); Neuroblastoma; LUNG-CANCER; BIOMARKERS; NSE;
D O I
10.1016/j.aca.2012.02.007
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
To detect a biomarker for small cell lung carcinoma, neuron specific enolase (NSE), a sensitive and specific chemiluminescence enzyme immunoassay was developed. Fluorescein isothiocyanate (FITC) labeled NSE capture antibody connected with NSE and alkaline phosphatase (ALP) labeled NSE detection antibody in a sandwich-type detection manner. This immune complex was further reacted with anti-FITC coated magnetic beads. In a magnetic field, the complex was enriched, and the sensitivity was thus enhanced. The limit of detection (LOD) of this method was <0.2 ng mL(-1). The proposed immunoassay was highly selective, and not interfered by hook effect. The recovery was >83.0% and the coefficient of variation was <10.0%. Human sera from 120 patients were tested with the presented and traditional chemiluminescence enzyme immunoassay. An excellent linear relationship was obtained between two techniques. Overall. this immunoassay offers a promising alternative for NSE detection than traditional clinical examinations. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:114 / 118
页数:5
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