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Co3O4/Au Hybrid Nanostructures as Efficient Peroxidase Mimics for Colorimetric Biosensing

Authors
Kim, Ji SeonJang, Ji YeonCheon, Hong JaeCho, SeongyeonJang, In SeungYu, Byung JoKim, Moon Il
Issue Date
Oct-2019
Publisher
AMER SCIENTIFIC PUBLISHERS
Keywords
Hybrid Nanostructures; Peroxidase Mimics; Cobalt Oxide Nanoparticles; Gold Nanoclusters; Colorimetric Biosensing
Citation
JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, v.19, no.10, pp.6696 - 6702
Journal Title
JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY
Volume
19
Number
10
Start Page
6696
End Page
6702
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/927
DOI
10.1166/jnn.2019.17098
ISSN
1533-4880
Abstract
Nanomaterials with enzyme-like characteristics (nanozymes) have emerged as potential replacements for natural enzymes due to their potential to overcome several critical limitations of natural enzymes, including low stability as well as high costs in preparation and purification. Herein, we have developed hybrid nanostructures that incorporate cobalt oxide nanoparticles (Co3O4 NPs) and gold nanoclusters (AuNCs) through electrostatic attraction induced by simple incubation in an aqueous buffer for 2 hours. Owing to the synergistic effect of Co3O4 NPs and AuNCs, the constructed Co3O4/Au hybrid nanostructures yielded highly enhanced peroxidase-like activity and enabled rapid catalytic oxidation of a chromogenic substrate, 3,3',5,5'-tetramethylbenzidine (TMB), producing a blue colored solution depending on the amount of H2O2. Moreover, we observed catalytic activity of the Co3O4/Au hybrid over a broad pH range, especially at physiologically relevant pH in the range of 5.0-7.4, which is advantageous for applications in biological systems. Using the hybrid as peroxidase mimic, we successfully determined the level of target H2O2 or glucose by coupling with glucose oxidase with excellent specificity and sensitivity. Based on this study, we expect that Co3O4/Au hybrid nanostructures can serve as potent peroxidase mimics for the detection of clinically important target molecules.
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