Chemiluminescence flow biosensor for hydrogen peroxide using DNAzyme immobilized on eggshell membrane as a thermally stable biocatalyst

被引:107
作者
Chen, Weiwei [1 ]
Li, Baoxin [1 ]
Xu, Chunli [1 ]
Wang, Lei [1 ]
机构
[1] Shaanxi Normal Univ, Sch Chem & Mat Sci, Key Lab Analyt Chem Life Sci Shaanxi Prov, Xian 710062, Peoples R China
基金
中国国家自然科学基金;
关键词
Chemiluminescence; DNAzyme; Eggshell membrane; Biosensor; Hydrogen peroxide; AMPLIFIED DETECTION; TELOMERASE ACTIVITY; HEMIN COMPLEX; DNA; ENZYME; NANOPARTICLES; GLUCOSE; CATALYST; MODELS; ACID;
D O I
10.1016/j.bios.2009.01.010
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A DNAzyme-based chemiluminescence (CL) biosensor for sensitive detection of hydrogen peroxide (H2O2) has been developed. The complexation of hemin with a guanine-rich single-stranded nucleic acid yields the DNAzyme with peroxidase catalytic activity. The DNAzyme catalyzes the oxidation of luminol by H2O2 and the generation of CL. The DNAzyme is immobilized on eggshell membrane, and then packed into mini-column as CL flow cell. In the presence of luminol, H2O2 passed through the CL flow cell to produce CL emission, and then was sensed. The response to H2O2 concentration was linear in the range of 1 x 10(-5)-1 x 10(-7) M with a detection limit of 5 x 10(-8) M (3 sigma). Compared to the HRP-based biosensor for H2O2, the DNAzyme possessed high catalytic activity in strong alkaline medium, which was well compatible with the luminol CL system. The immobilized DNAzyme could be stored at room temperature (similar to 20 degrees C) and exhibited good stability with a shelf life of at least 3 months. A complete analysis, including sample and washing, could be performed in 1 min with a relative standard deviation of less than 2%. This biosensor for H2O2 has the potential to serve as a general platform for design sensors for other molecules (such as glucose and uric acid). (c) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:2534 / 2540
页数:7
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