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Glucose Sensor Using Redox Active Oligonucleotide-Templated Silver Nanoclusters

Redox active, photoluminescent silver nanoclusters templated with oligonucleotides were developed for glucose sensing. The silver nanoclusters had a photoluminescent emission at 610 nm that reversibly changed to 530 nm upon oxidation. The reversible emission change was measured with photoluminescent...

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Detalles Bibliográficos
Autores principales: Schroeder, Kathryn L., Goreham, Renee V., Nann, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722757/
https://www.ncbi.nlm.nih.gov/pubmed/31344954
http://dx.doi.org/10.3390/nano9081065
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author Schroeder, Kathryn L.
Goreham, Renee V.
Nann, Thomas
author_facet Schroeder, Kathryn L.
Goreham, Renee V.
Nann, Thomas
author_sort Schroeder, Kathryn L.
collection PubMed
description Redox active, photoluminescent silver nanoclusters templated with oligonucleotides were developed for glucose sensing. The silver nanoclusters had a photoluminescent emission at 610 nm that reversibly changed to 530 nm upon oxidation. The reversible emission change was measured with photoluminescent spectroscopy and used to detect H(2)O(2), which is a by-product of the reaction of glucose with glucose oxidase. The ratio of the un-oxidised emission peak (610 nm) and the oxidised analogue (530 nm) was used to measure glucose concentrations up to 20 mM, well within glucose levels found in blood. Also, the reversibility of this system enables the silver nanoclusters to be reused.
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spelling pubmed-67227572019-09-10 Glucose Sensor Using Redox Active Oligonucleotide-Templated Silver Nanoclusters Schroeder, Kathryn L. Goreham, Renee V. Nann, Thomas Nanomaterials (Basel) Article Redox active, photoluminescent silver nanoclusters templated with oligonucleotides were developed for glucose sensing. The silver nanoclusters had a photoluminescent emission at 610 nm that reversibly changed to 530 nm upon oxidation. The reversible emission change was measured with photoluminescent spectroscopy and used to detect H(2)O(2), which is a by-product of the reaction of glucose with glucose oxidase. The ratio of the un-oxidised emission peak (610 nm) and the oxidised analogue (530 nm) was used to measure glucose concentrations up to 20 mM, well within glucose levels found in blood. Also, the reversibility of this system enables the silver nanoclusters to be reused. MDPI 2019-07-24 /pmc/articles/PMC6722757/ /pubmed/31344954 http://dx.doi.org/10.3390/nano9081065 Text en © 2019 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
Schroeder, Kathryn L.
Goreham, Renee V.
Nann, Thomas
Glucose Sensor Using Redox Active Oligonucleotide-Templated Silver Nanoclusters
title Glucose Sensor Using Redox Active Oligonucleotide-Templated Silver Nanoclusters
title_full Glucose Sensor Using Redox Active Oligonucleotide-Templated Silver Nanoclusters
title_fullStr Glucose Sensor Using Redox Active Oligonucleotide-Templated Silver Nanoclusters
title_full_unstemmed Glucose Sensor Using Redox Active Oligonucleotide-Templated Silver Nanoclusters
title_short Glucose Sensor Using Redox Active Oligonucleotide-Templated Silver Nanoclusters
title_sort glucose sensor using redox active oligonucleotide-templated silver nanoclusters
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722757/
https://www.ncbi.nlm.nih.gov/pubmed/31344954
http://dx.doi.org/10.3390/nano9081065
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