Hypersensitive electrochemical immunoassays based on highly N-doped silicon carbide (SiC) electrode

Authors
Park, Jun-HeeSong, ZhiquanLee, Ga-YeonJeong, Seong-MinKang, Min-JungPyun, Jae-Chul
Issue Date
2019-09-27
Publisher
ELSEVIER SCIENCE BV
Citation
ANALYTICA CHIMICA ACTA, v.1073, pp.30 - 38
Abstract
Highly N-doped SiC was presented as an optimal electrode for electrochemical immunoassays with a far higher sensitivity than chemiluminescence detection. As the first step, the electrochemical properties of highly N-doped SiC, such as the double-layer capacitance (C-dl), rate constant for electron transfer (k(app)) and ideal polarizable potential range (electrochemical window) were analyzed and compared with those of Au, Pt, and graphite electrodes. The highly N-doped SiC electrode was used for the quantification of oxidized 3,3',5,5'-tetramethylbenzidine (TMB) which was widely used as chromogenic substrate for commercialized immunoassay kits. In order to enhance the sensitivity for the quantification of the oxidized TMB the chronoamperometry was applied to avoid the background current of i-V measurement. Finally, the chronoamperometry based on the highly N-doped SiC electrode was applied to commercial immunoassay kits for the medical diagnosis of the human immunodeficiency virus (HIV) and the human hepatitis B surface antigen (hHBsAg). The chronoamperometric measurement based on the highly N-doped SiC electrode was proved to detect at far lower limits in comparison with the conventional optical density measurement as well as the chemiluminescence assay based on luminol as a chemiluminescent probe. (C) 2019 Elsevier B.V. All rights reserved.
Keywords
TRANSFER KINETICS; HIGH-TEMPERATURE; SEMICONDUCTOR; GOLD; OXIDATION; BEHAVIOR; OXYGEN; TRANSFER KINETICS; HIGH-TEMPERATURE; SEMICONDUCTOR; GOLD; OXIDATION; BEHAVIOR; OXYGEN; SiC; Immunoassay; Chronoamperometry; Chemiluminescence; Medical diagnosis
ISSN
0003-2670
URI
https://pubs.kist.re.kr/handle/201004/119554
DOI
10.1016/j.aca.2019.04.054
Appears in Collections:
KIST Article > 2019
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