Cargando…
Enzyme-Regulated In Situ Formation of Copper Hexacyanoferrate Nanoparticles with Oxidase-Mimetic Behaviour for Colorimetric Detection of Ascorbate Oxidase
In this study, a copper hexacyanoferrate nanoparticle with excellent oxidase-mimetic behaviour has been synthesized through a simple precipitation method. The synthesized copper hexacyanoferrate nanoparticle has intrinsic oxidase-like activity, which can catalyze the chromogenic reaction of 2,2′-azi...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10046506/ https://www.ncbi.nlm.nih.gov/pubmed/36979556 http://dx.doi.org/10.3390/bios13030344 |
_version_ | 1785013689705824256 |
---|---|
author | Zhang, Hao Yang, Dan-Ni Li, Yan Yang, Feng-Qing |
author_facet | Zhang, Hao Yang, Dan-Ni Li, Yan Yang, Feng-Qing |
author_sort | Zhang, Hao |
collection | PubMed |
description | In this study, a copper hexacyanoferrate nanoparticle with excellent oxidase-mimetic behaviour has been synthesized through a simple precipitation method. The synthesized copper hexacyanoferrate nanoparticle has intrinsic oxidase-like activity, which can catalyze the chromogenic reaction of 2,2′-azinobis-(3-ethylbenzthiazoline-6-sulphonate) through an O(2)(•−) reactive oxygen-species-participated process. On the other hand, K(3)[Fe(CN)(6)] can be reduced by ascorbic acid (AA) to produce K(4)[Fe(CN)(6)], thereby inhibiting the formation of the copper hexacyanoferrate nanoparticles. Furthermore, ascorbate oxidase (AAO) can catalyze the oxidation of AA to produce dehydroascorbic acid, which cannot reduce K(3)[Fe(CN)(6)]. Thus, a system for an AAO-regulated in situ formation of copper hexacyanoferrate nanoparticles was constructed by coupling a prepared copper hexacyanoferrate nanozyme with AA for the detection of AAO activity. This colorimetric sensing assay shows high sensitivity and selectivity for the detection of AAO activity (the limit of detection is 0.52 U/L) with a linear range of 1.1–35.7 U/L. Finally, the developed method was applied to detect the activity of AAO in normal human serum with a satisfactory sample spiked recovery (87.4–108.8%). In short, this study provides a good strategy for the construction of nanozyme-based multi-enzyme cascade-signal amplification assay. |
format | Online Article Text |
id | pubmed-10046506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100465062023-03-29 Enzyme-Regulated In Situ Formation of Copper Hexacyanoferrate Nanoparticles with Oxidase-Mimetic Behaviour for Colorimetric Detection of Ascorbate Oxidase Zhang, Hao Yang, Dan-Ni Li, Yan Yang, Feng-Qing Biosensors (Basel) Article In this study, a copper hexacyanoferrate nanoparticle with excellent oxidase-mimetic behaviour has been synthesized through a simple precipitation method. The synthesized copper hexacyanoferrate nanoparticle has intrinsic oxidase-like activity, which can catalyze the chromogenic reaction of 2,2′-azinobis-(3-ethylbenzthiazoline-6-sulphonate) through an O(2)(•−) reactive oxygen-species-participated process. On the other hand, K(3)[Fe(CN)(6)] can be reduced by ascorbic acid (AA) to produce K(4)[Fe(CN)(6)], thereby inhibiting the formation of the copper hexacyanoferrate nanoparticles. Furthermore, ascorbate oxidase (AAO) can catalyze the oxidation of AA to produce dehydroascorbic acid, which cannot reduce K(3)[Fe(CN)(6)]. Thus, a system for an AAO-regulated in situ formation of copper hexacyanoferrate nanoparticles was constructed by coupling a prepared copper hexacyanoferrate nanozyme with AA for the detection of AAO activity. This colorimetric sensing assay shows high sensitivity and selectivity for the detection of AAO activity (the limit of detection is 0.52 U/L) with a linear range of 1.1–35.7 U/L. Finally, the developed method was applied to detect the activity of AAO in normal human serum with a satisfactory sample spiked recovery (87.4–108.8%). In short, this study provides a good strategy for the construction of nanozyme-based multi-enzyme cascade-signal amplification assay. MDPI 2023-03-04 /pmc/articles/PMC10046506/ /pubmed/36979556 http://dx.doi.org/10.3390/bios13030344 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhang, Hao Yang, Dan-Ni Li, Yan Yang, Feng-Qing Enzyme-Regulated In Situ Formation of Copper Hexacyanoferrate Nanoparticles with Oxidase-Mimetic Behaviour for Colorimetric Detection of Ascorbate Oxidase |
title | Enzyme-Regulated In Situ Formation of Copper Hexacyanoferrate Nanoparticles with Oxidase-Mimetic Behaviour for Colorimetric Detection of Ascorbate Oxidase |
title_full | Enzyme-Regulated In Situ Formation of Copper Hexacyanoferrate Nanoparticles with Oxidase-Mimetic Behaviour for Colorimetric Detection of Ascorbate Oxidase |
title_fullStr | Enzyme-Regulated In Situ Formation of Copper Hexacyanoferrate Nanoparticles with Oxidase-Mimetic Behaviour for Colorimetric Detection of Ascorbate Oxidase |
title_full_unstemmed | Enzyme-Regulated In Situ Formation of Copper Hexacyanoferrate Nanoparticles with Oxidase-Mimetic Behaviour for Colorimetric Detection of Ascorbate Oxidase |
title_short | Enzyme-Regulated In Situ Formation of Copper Hexacyanoferrate Nanoparticles with Oxidase-Mimetic Behaviour for Colorimetric Detection of Ascorbate Oxidase |
title_sort | enzyme-regulated in situ formation of copper hexacyanoferrate nanoparticles with oxidase-mimetic behaviour for colorimetric detection of ascorbate oxidase |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10046506/ https://www.ncbi.nlm.nih.gov/pubmed/36979556 http://dx.doi.org/10.3390/bios13030344 |
work_keys_str_mv | AT zhanghao enzymeregulatedinsituformationofcopperhexacyanoferratenanoparticleswithoxidasemimeticbehaviourforcolorimetricdetectionofascorbateoxidase AT yangdanni enzymeregulatedinsituformationofcopperhexacyanoferratenanoparticleswithoxidasemimeticbehaviourforcolorimetricdetectionofascorbateoxidase AT liyan enzymeregulatedinsituformationofcopperhexacyanoferratenanoparticleswithoxidasemimeticbehaviourforcolorimetricdetectionofascorbateoxidase AT yangfengqing enzymeregulatedinsituformationofcopperhexacyanoferratenanoparticleswithoxidasemimeticbehaviourforcolorimetricdetectionofascorbateoxidase |