Capillary electrophoretic immunoassay for alpha-fetoprotein with chemiluminescence detection

被引:31
作者
Liu, Yan-Ming [1 ]
Mu, Hai-Bei
Zheng, Yan-Li
Wang, Cheng-Quan
Chen, Yong-Hong
Li, Fu-Rong
Wang, Jun-Hua
Cheng, Jie-Ke
机构
[1] Xinyang Normal Univ, Coll Chem & Chem Engn, Xinyang 464000, Peoples R China
[2] Xinyang Cent Hosp, Xinyang 464000, Peoples R China
[3] Xinyang Normal Univ, Coll Life Sci, Xining 464000, Peoples R China
[4] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2007年 / 855卷 / 02期
基金
中国国家自然科学基金;
关键词
capillary electrophoresis; enzyme immunoassay; chemiluminescence detection; alpha-fetoprotein;
D O I
10.1016/j.jchromb.2007.04.033
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A capillary electrophoretic immunoassay with chemiluminescence detection (CEIA-CL) using a non-competitive format for analyzing tumor marker alpha-fetoprotein (AFP) has been developed. In this method, antigen (Ag) AFP reacts with an excess amount of horseradish peroxidase (HRP)-labeled antibody (Ab*). The free Ab* and the bound Ab*-Ag complex produced in the solution are separated by CE in a separation capillary. Then they catalyze the reaction of enzyme substrate luminol and H2O2 in a reaction capillary following the separation capillary. Parameters affecting the CE separation and CL detection were investigated. Under the optimal conditions, the free Ab* and the Ab*-Ag complex were well separated within 4 min, the linear range and the detection limit (S/N = 3) for AFP were 5-500 ng/ml and 0.85 ng/ml (1.2 x 10(-11) M), respectively. The proposed method has been applied satisfactorily in the analysis of human sera samples. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:280 / 285
页数:6
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