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Effective Peroxidase-Like Activity of Co-Aminoclay [CoAC] and Its Application for Glucose Detection
In this study, we describe a novel peroxidase-like activity of Co-aminoclay [CoAC] present at pH ~5.0 and its application to fluorescent biosensor for the determination of H(2)O(2) and glucose. It is synthesized with aminoclays (ACs) entrapping cationic metals such as Fe, Cu, Al, Co., Ce, Ni, Mn, an...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5855466/ https://www.ncbi.nlm.nih.gov/pubmed/29401685 http://dx.doi.org/10.3390/s18020457 |
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author | Song, Han Pill Lee, Yongil Bui, Vu Khac Hoang Oh, You-Kwon Park, Hyun Gyu Kim, Moon Il Lee, Young-Chul |
author_facet | Song, Han Pill Lee, Yongil Bui, Vu Khac Hoang Oh, You-Kwon Park, Hyun Gyu Kim, Moon Il Lee, Young-Chul |
author_sort | Song, Han Pill |
collection | PubMed |
description | In this study, we describe a novel peroxidase-like activity of Co-aminoclay [CoAC] present at pH ~5.0 and its application to fluorescent biosensor for the determination of H(2)O(2) and glucose. It is synthesized with aminoclays (ACs) entrapping cationic metals such as Fe, Cu, Al, Co., Ce, Ni, Mn, and Zn to find enzyme mimicking ACs by sol–gel ambient conditions. Through the screening of catalytic activities by the typical colorimetric reaction employing 2,2′-azino-bis(3-ethylbenzo-thiazoline-6-sulfonic acid)diammonium salt (ABTS) as a substrate with or without H(2)O(2), Fe, Cu, and CoACs are found to exhibit peroxidase-like activity, as well as oxidase-like activity was observed from Ce and MnACs. Among them, CoAC shows exceptionally high peroxidase-like activity, presumably due to its ability to induce electron transfer between substrates and H(2)O(2). CoAC is then used to catalyze the oxidation of Amplex(®) UltraRed (AUR) into a fluorescent end product, which enables a sensitive fluorescent detection of H(2)O(2). Moreover, a highly sensitive and selective glucose biosensing strategy is developed, based on enzyme cascade reaction between glucose oxidase (GOx) and CoAC. Using this strategy, a highly linear fluorescence enhancement is verified when the concentration of glucose is increased in a wide range from 10 μM to 1 mM with a lower detection limit of 5 μM. The practical diagnostic capability of the assay system is also verified by its use to detect glucose in human blood serum. Based on these results, it is anticipated that CoAC can serve as potent peroxidase mimetics for the detection of clinically important target molecules. |
format | Online Article Text |
id | pubmed-5855466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-58554662018-03-20 Effective Peroxidase-Like Activity of Co-Aminoclay [CoAC] and Its Application for Glucose Detection Song, Han Pill Lee, Yongil Bui, Vu Khac Hoang Oh, You-Kwon Park, Hyun Gyu Kim, Moon Il Lee, Young-Chul Sensors (Basel) Article In this study, we describe a novel peroxidase-like activity of Co-aminoclay [CoAC] present at pH ~5.0 and its application to fluorescent biosensor for the determination of H(2)O(2) and glucose. It is synthesized with aminoclays (ACs) entrapping cationic metals such as Fe, Cu, Al, Co., Ce, Ni, Mn, and Zn to find enzyme mimicking ACs by sol–gel ambient conditions. Through the screening of catalytic activities by the typical colorimetric reaction employing 2,2′-azino-bis(3-ethylbenzo-thiazoline-6-sulfonic acid)diammonium salt (ABTS) as a substrate with or without H(2)O(2), Fe, Cu, and CoACs are found to exhibit peroxidase-like activity, as well as oxidase-like activity was observed from Ce and MnACs. Among them, CoAC shows exceptionally high peroxidase-like activity, presumably due to its ability to induce electron transfer between substrates and H(2)O(2). CoAC is then used to catalyze the oxidation of Amplex(®) UltraRed (AUR) into a fluorescent end product, which enables a sensitive fluorescent detection of H(2)O(2). Moreover, a highly sensitive and selective glucose biosensing strategy is developed, based on enzyme cascade reaction between glucose oxidase (GOx) and CoAC. Using this strategy, a highly linear fluorescence enhancement is verified when the concentration of glucose is increased in a wide range from 10 μM to 1 mM with a lower detection limit of 5 μM. The practical diagnostic capability of the assay system is also verified by its use to detect glucose in human blood serum. Based on these results, it is anticipated that CoAC can serve as potent peroxidase mimetics for the detection of clinically important target molecules. MDPI 2018-02-03 /pmc/articles/PMC5855466/ /pubmed/29401685 http://dx.doi.org/10.3390/s18020457 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Song, Han Pill Lee, Yongil Bui, Vu Khac Hoang Oh, You-Kwon Park, Hyun Gyu Kim, Moon Il Lee, Young-Chul Effective Peroxidase-Like Activity of Co-Aminoclay [CoAC] and Its Application for Glucose Detection |
title | Effective Peroxidase-Like Activity of Co-Aminoclay [CoAC] and Its Application for Glucose Detection |
title_full | Effective Peroxidase-Like Activity of Co-Aminoclay [CoAC] and Its Application for Glucose Detection |
title_fullStr | Effective Peroxidase-Like Activity of Co-Aminoclay [CoAC] and Its Application for Glucose Detection |
title_full_unstemmed | Effective Peroxidase-Like Activity of Co-Aminoclay [CoAC] and Its Application for Glucose Detection |
title_short | Effective Peroxidase-Like Activity of Co-Aminoclay [CoAC] and Its Application for Glucose Detection |
title_sort | effective peroxidase-like activity of co-aminoclay [coac] and its application for glucose detection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5855466/ https://www.ncbi.nlm.nih.gov/pubmed/29401685 http://dx.doi.org/10.3390/s18020457 |
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