A colorimetric and electrochemical dual-mode biosensor for thrombin using a magnetic separation technique

被引:30
作者
Guo, Wen-Jing [1 ]
Yang, Xiao-Yan [1 ]
Wu, Zhen [2 ]
Zhang, Zhi-Ling [1 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Minist Educ, Key Lab Analyt Chem Biol & Med, Wuhan 430072, Peoples R China
[2] Hubei Univ, Coll Chem & Chem Engn, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Minist Educ,Key Lab Synth & Applicat Organ Funct, Wuhan 430062, Peoples R China
基金
中国国家自然科学基金;
关键词
HYBRIDIZATION CHAIN-REACTION; HIGHLY SENSITIVE DETECTION; SALMONELLA-TYPHIMURIUM; APTAMER SENSOR; PROTEIN; AMPLIFICATION; FLUORESCENCE; DNA; CAPTURE; NANOSPHERES;
D O I
10.1039/c9tb02170a
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
In general, protein detection relies primarily on enzyme-linked immunosorbent assays. Here, we constructed a colorimetric and electrochemical dual-mode biosensor for thrombin detection based on the mechanism of aptamer recognition. Magnetic nanobeads (MBs) were used as carriers for separation and enrichment to quickly capture thrombin (TB) in the complex matrix. Also, the combination of MBs and the magnetic electrode array (MEA) effectively avoided the poisoning of the electrode by biological samples. Furthermore, hybridization chain reaction (HCR) was indirectly used to achieve amplification of TB. A large number of horseradish peroxidases (HRPs) were coupled with the amplified long nucleic acid fragments. Based on the color and current response of the substrate TMB catalyzed by HRP, a dual-mode detection system for thrombin was established to ensure the accuracy of the test results. The method had a minimum resolution of 10 nM to the naked eye and an electrochemical detection limit as low as 0.35 nM. In addition, the sensor provided good anti-interference ability in a complex matrix and showed great potential to detect TB in complex samples.
引用
收藏
页码:3574 / 3581
页数:8
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