Ru(bpy)32+-doped silica nanoparticle DNA probe for the electrogenerated chemiluminescence detection of DNA hybridization

被引:94
作者
Chang, Zhu
Zhou, Jingming
Zhao, Kun
Zhu, Ningning
He, Pingang
Fang, Yuzhi [1 ]
机构
[1] E China Normal Univ, Dept Chem, Shanghai 200062, Peoples R China
[2] Shanghai Teachers Coll, Dept Chem, Shanghai 476000, Peoples R China
[3] Shanghai Normal Univ, Dept Chem, Shanghai 200234, Peoples R China
基金
中国国家自然科学基金;
关键词
Ru(bPY)(3)(2+); silica nanoparticles; electrogenerated chemiluminescence; DNA hybridization;
D O I
10.1016/j.electacta.2006.05.036
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A sensitive electrogenerated chemiluminescence (ECL) detection of DNA hybridization, based on tris(2,2'-bipyridyl)ruthenium(II)-doped silica nanoparticles (Ru(bpy)(3)(2+) -doped SNPs) as DNA tags, is described. In this protocol, Ru(bPY)(3)(2+) -doped SNPs was used for DNA labeling with trimethoxysilylpropydiethylenetriamine(DETA) and glutaraldehyde as linking agents. The Ru(bPY)(3)(2+) -doped SNPs labeled DNA probe was hybridized with target DNA immobilized on the surface of polypyrrole (PPy) modified Pt electrode. The hybridization events were evaluated by ECL measurements and only the complementary sequence could form a double-stranded DNA (dsDNA) with DNA probe and give strong ECL signals. A three-base mismatch sequence and a non-complementary sequence had almost negligible responses. Due to the large number of Ru(bPY)(3)(2+) molecules inside SNPs, the assay allows detection at levels as low as 1.0 X 10(-13) Mol l(-1) of the target DNA. The intensity of ECL was linearly related to the concentration of the complementary sequence in the range of 2.0 x 10(-13) to 2.0 x 10(-9) mol l(-1). (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:575 / 580
页数:6
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