Gold nanoparticles modified electrode via a mercapto-diazoaminobenzene monolayer and its development in DNA electrochemical biosensor

2010 ◽  
Vol 25 (9) ◽  
pp. 2084-2088 ◽  
Author(s):  
Feng Li ◽  
Yan Feng ◽  
Pingjun Dong ◽  
Bo Tang
2011 ◽  
Vol 298 ◽  
pp. 128-134
Author(s):  
Ai Chun Zhang ◽  
Cun Zhou

In this paper, a novel DNA electrochemical biosensor based on layer-by-layer self-assembled technology was reported. Gold nanoparticles were firstly immobilized on chitosan modified gold electrode by large amino of chitosan because of strong electrostatic adsorption effect between amino and gold atom, and thoil group modified DNA (SH-ssDNA) probe sequence was then self-assembled onto the electrode. Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were applied to investigate the electrochemical behavior of different modified electrodes with methylene blue as hybrid indicator. The results in optimization experiment condition show that: The peak current difference value pre and post hybridization was linearly related to the logatithmic value of the target DNA concentration ranging from 10-8~10-5mol/L.A detection limit of 3.55×10-9mol/L can be estimated.


2011 ◽  
Vol 298 ◽  
pp. 135-141 ◽  
Author(s):  
Cun Zhou ◽  
Ai Chun Zhang

In this paper, an efficient process for preparing monodisperse gold nanoparticles coated with silica shells (Au@SiO2) was reported, and a novel DNA electrochemical biosensor based on layer-by-layer self-assembled technology as well as Au@SiO2 nanoparticles was presented. Chitosan was immobilized on gold electrode by good film-forming property and lots of amino because of strong electrostatic adsorption effect between amino and gold atom, Au@SiO2 nanoparticles were also immobilized to the electrode in that it kept the excellent features of gold nanoparticles, therefore, thoil group modified DNA (SH-ssDNA) probe sequence can self-assembled on Au@SiO2 nanoparticles modified electrode with the purpose of realize quantitative detection of complementary DNA. Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were applied to investigate the electrochemical behavior of different modified electrodes with methylene blue as hybrid indicator. The results in optimization experiment condition show that: the peak current difference value pre and post hybridization was linearly related to the logatithmic value of the target DNA concentration ranging from 10-10~10-6mol/L. A detection limit of 4.02×10-11mol/L can be estimated.


2021 ◽  
pp. 107801
Author(s):  
José M. R. Flauzino ◽  
Rafaela C. S. Peres ◽  
Lívia M. Alves ◽  
Jussara G. Vieira ◽  
Júlia G. dos Santos ◽  
...  

The Analyst ◽  
2021 ◽  
Vol 146 (8) ◽  
pp. 2679-2688
Author(s):  
Chammari Pothipor ◽  
Noppadol Aroonyadet ◽  
Suwussa Bamrungsap ◽  
Jaroon Jakmunee ◽  
Kontad Ounnunkad

An ultrasensitive electrochemical biosensor based on a gold nanoparticles/graphene/polypyrrole composite modified electrode and a signal amplification strategy employing methylene blue is developed as a potential tool for the detection of miRNA-21.


2011 ◽  
Vol 239-242 ◽  
pp. 2499-2502
Author(s):  
Nan Nan Wei ◽  
Jiang Yan Du

A new electrochemical biosensor based on the immobilization of horseradish peroxidase(HRP) on TiO2 nanoneedles modified electrodes has been fabricated. The direct electrochemical response of HRP immobilized on the modified electrode was dramatically enhanced. The immobilized HRP displayed a couple of stable and well-defined redox peaks with a formal potential of -0.379 V (vs. SCE). The HRP/TiO2 nanoneedles modified electrode exhibited a remarkable electrocatalytic activity toward the oxidation of H2O2. The amperometric response to H2O2 showed a linear range of 4–700μmol/L, with the calculated detection limit of 0.78 μmol/L at a signal-to-noise ratio of three. The modified electrode displayed an acceptable reproducibility and good stability. The new HRP/TiO2 nanoneedles matrix is expected to have wide applications for enzymes and proteins immobilization and direct electron transfer study and opened a way for low conductivity electrode biosensors.


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