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Sensitive and high-fidelity electrochemical immunoassay using carbon nanotubes coated with enzymes and magnetic nanoparticles

Authors
Piao, YunxianJin, ZongwenLee, DohoonLee, Hye-JinNa, Hyon-BinHyeon, TaeghwanOh, Min-KyuKim, JungbaeKim, Hak-Sung
Issue Date
15-3월-2011
Publisher
ELSEVIER ADVANCED TECHNOLOGY
Keywords
Enzyme coating; Electrochemical immunoassay; Substrate recycling; Carbon nanotube; Tyrosinase
Citation
BIOSENSORS & BIOELECTRONICS, v.26, no.7, pp.3192 - 3199
Indexed
SCIE
SCOPUS
Journal Title
BIOSENSORS & BIOELECTRONICS
Volume
26
Number
7
Start Page
3192
End Page
3199
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/112843
DOI
10.1016/j.bios.2010.12.025
ISSN
0956-5663
Abstract
We demonstrate a highly sensitive electrochemical immunosensor based on the combined use of substrate recycling and carbon nanotubes (CNTs) coated with tyrosinase (TYR) and magnetic nanoparticles (MNP). Both TYR and MNP were immobilized on the surface of CNTs by covalent attachment, followed by additional cross-linking via glutaraldehyde treatment to construct multi-layered cross-linked TYR-MNP aggregates (M-EC-CNT). Magnetically capturable, highly active and stable M-EC-CNT were further conjugated with primary antibody against a target analyte of hIgG, and used for a sandwich-type immunoassay with a secondary antibody conjugated with alkaline phosphatase (ALP). In the presence of a target analyte, a sensing assembly of M-EC-CNT and ALP-conjugated antibody was attracted onto a gold electrode using a magnet. On an electrode, ALP-catalyzed hydrolysis of phenyl phosphate generated phenol, and successive TYR-catalyzed oxidation of phenol produced electrochemically measurable o-quinone that was converted to catechol in a scheme of substrate recycling. Combination of highly active M-EC-CNT and substrate recycling for the detection of hIgG resulted in a sensitivity of 27.6 nA ng(-1) mL(-1) and a detection limit of 0.19 ng mL(-1) (1.2 pM), respectively, representing better performance than any other electrochemical immunosensors relying on the substrate recycling with the TYR-ALP combination. The present immunosensing system also displayed a long-term stability by showing a negligible loss of electrochemical detection signal even after reagents were stored in an aqueous buffer at 4 degrees C for more than 6 months. (C) 2010 Elsevier B.V. All rights reserved.
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