Facile degradation of benzenediazonium-grafted thick layers on the electrode surface enabling electrochemical biosensor application

2013 ◽  
Vol 49 (36) ◽  
pp. 3802 ◽  
Author(s):  
Al-Monsur Jiaul Haque ◽  
Md. Mohibul Islam Khan ◽  
Kyuwon Kim
2019 ◽  
Vol 19 ◽  
pp. 1183-1188
Author(s):  
Suhaili Sabdin ◽  
Mohd Azraie Mohd Azmi ◽  
Nurul Azurin Badruzaman ◽  
Fatihatul Zuriati Makmon ◽  
Azman Abd Aziz ◽  
...  

The Analyst ◽  
2014 ◽  
Vol 139 (9) ◽  
pp. 2193-2198 ◽  
Author(s):  
Yun Zhang ◽  
Fang Liu ◽  
Jinfang Nie ◽  
Fuyang Jiang ◽  
Caibin Zhou ◽  
...  

This paper describes for the first time an electrochemical biosensor, which employs a DNA probe modified with a redox tag close to electrode surface, for picomolar detection of a sequence-specific DNA-binding protein.


RSC Advances ◽  
2015 ◽  
Vol 5 (30) ◽  
pp. 23395-23400 ◽  
Author(s):  
Seung-Koo Lee ◽  
Min-Jung Song ◽  
Jong-Hoon Kim ◽  
Young-Kyun Lim ◽  
Yoon-Soo Chun ◽  
...  

Selective growth of MWCNTs on boron-doped diamond electrode was introduced and their electrochemical properties and glucose biosensing performances were reported.


2015 ◽  
Vol 18 (3) ◽  
pp. 135-144
Author(s):  
Tien Huu Cao ◽  
Linh Van Ha ◽  
Hieu Van Le

The optimization of DNA probe immobilisation on gold electrode surface is very important to develop DNA biosensors. In this study, we conducted an experiment to determine the optimal concentration of probe attached on the electrodes and probe immobilization agent (mercaptohexanol) for maximum hybridization efficacy. We have used a method to control the surface density of DNA probe by annealing probe modified by thiol and mercaptohexanol. With linear relationship between molar ratio and surface density of probe, by controlling probe concentration in sensor fabricating process, we can determine the molecular density of DNA probes on electrode surface. The results show that probe concentration 500 nM and 1.5 mM mercaptohaxenol are optimal for hybidization with DNA target.


Sensors ◽  
2016 ◽  
Vol 16 (5) ◽  
pp. 660 ◽  
Author(s):  
Taek Lee ◽  
Tae-Hyung Kim ◽  
Jinho Yoon ◽  
Yong-Ho Chung ◽  
Ji Lee ◽  
...  

Sensors ◽  
2021 ◽  
Vol 21 (4) ◽  
pp. 1125 ◽  
Author(s):  
Ana-Maria Chiorcea-Paquim ◽  
Ana Maria Oliveira-Brett

Deoxyribonucleic acid (DNA) electrochemical biosensors are devices that incorporate immobilized DNA as a molecular recognition element on the electrode surface, and enable probing in situ the oxidative DNA damage. A wide range of DNA electrochemical biosensor analytical and biotechnological applications in pharmacology are foreseen, due to their ability to determine in situ and in real-time the DNA interaction mechanisms with pharmaceutical drugs, as well as with their degradation products, redox reaction products, and metabolites, and due to their capacity to achieve quantitative electroanalytical evaluation of the drugs, with high sensitivity, short time of analysis, and low cost. This review presents the design and applications of label-free DNA electrochemical biosensors that use DNA direct electrochemical oxidation to detect oxidative DNA damage. The DNA electrochemical biosensor development, from the viewpoint of electrochemical and atomic force microscopy (AFM) characterization, and the bottom-up immobilization of DNA nanostructures at the electrode surface, are described. Applications of DNA electrochemical biosensors that enable the label-free detection of DNA interactions with pharmaceutical compounds, such as acridine derivatives, alkaloids, alkylating agents, alkylphosphocholines, antibiotics, antimetabolites, kinase inhibitors, immunomodulatory agents, metal complexes, nucleoside analogs, and phenolic compounds, which can be used in drug analysis and drug discovery, and may lead to future screening systems, are reviewed.


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