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Reagentless Amperometric Pyruvate Biosensor Based on a Prussian Blue- and Enzyme Nanoparticle-Modified Screen-Printed Carbon Electrode
[Image: see text] We report a facile strategy for developing reagentless amperometric pyruvate biosensors based on enzyme nanoparticles (EnNPs). The EnNPs were prepared using pyruvate oxidase crosslinked with graphene quantum dots. Before EnNP immobilization, screen-printed carbon electrodes (SPCEs)...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689939/ https://www.ncbi.nlm.nih.gov/pubmed/33251446 http://dx.doi.org/10.1021/acsomega.0c04522 |
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author | Thirumalai, Dinakaran Kim, Seonghye Kim, Suhkmann Chang, Seung-Cheol |
author_facet | Thirumalai, Dinakaran Kim, Seonghye Kim, Suhkmann Chang, Seung-Cheol |
author_sort | Thirumalai, Dinakaran |
collection | PubMed |
description | [Image: see text] We report a facile strategy for developing reagentless amperometric pyruvate biosensors based on enzyme nanoparticles (EnNPs). The EnNPs were prepared using pyruvate oxidase crosslinked with graphene quantum dots. Before EnNP immobilization, screen-printed carbon electrodes (SPCEs) were modified with Prussian blue, a biocompatible coordination polymer. The biosensor system was optimized in terms of the working potential and pH value. At pH 7.0 in 50 mM phosphate-buffered solution, the biosensor showed optimal characteristics under an applied potential of −0.10 V versus an internal pseudo-Ag reference electrode. Using these optimized conditions, the biosensor performance was characterized via the chronoamperometric technique. The EnNP-immobilized SPCE exhibited a dynamic linear range from 10 to 100 μM for pyruvate solution, and a sensitivity of 40.8 μA mM(–1) cm(–2) was recorded. The observed detection limit of the biosensor was 0.91 μM (S/N = 3) and it showed strong anti-inference capability under the optimized working potential. Furthermore, the practical applicability of the proposed biosensor was studied in fish serum samples. |
format | Online Article Text |
id | pubmed-7689939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-76899392020-11-27 Reagentless Amperometric Pyruvate Biosensor Based on a Prussian Blue- and Enzyme Nanoparticle-Modified Screen-Printed Carbon Electrode Thirumalai, Dinakaran Kim, Seonghye Kim, Suhkmann Chang, Seung-Cheol ACS Omega [Image: see text] We report a facile strategy for developing reagentless amperometric pyruvate biosensors based on enzyme nanoparticles (EnNPs). The EnNPs were prepared using pyruvate oxidase crosslinked with graphene quantum dots. Before EnNP immobilization, screen-printed carbon electrodes (SPCEs) were modified with Prussian blue, a biocompatible coordination polymer. The biosensor system was optimized in terms of the working potential and pH value. At pH 7.0 in 50 mM phosphate-buffered solution, the biosensor showed optimal characteristics under an applied potential of −0.10 V versus an internal pseudo-Ag reference electrode. Using these optimized conditions, the biosensor performance was characterized via the chronoamperometric technique. The EnNP-immobilized SPCE exhibited a dynamic linear range from 10 to 100 μM for pyruvate solution, and a sensitivity of 40.8 μA mM(–1) cm(–2) was recorded. The observed detection limit of the biosensor was 0.91 μM (S/N = 3) and it showed strong anti-inference capability under the optimized working potential. Furthermore, the practical applicability of the proposed biosensor was studied in fish serum samples. American Chemical Society 2020-11-11 /pmc/articles/PMC7689939/ /pubmed/33251446 http://dx.doi.org/10.1021/acsomega.0c04522 Text en © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Thirumalai, Dinakaran Kim, Seonghye Kim, Suhkmann Chang, Seung-Cheol Reagentless Amperometric Pyruvate Biosensor Based on a Prussian Blue- and Enzyme Nanoparticle-Modified Screen-Printed Carbon Electrode |
title | Reagentless Amperometric Pyruvate Biosensor Based
on a Prussian Blue- and Enzyme Nanoparticle-Modified Screen-Printed
Carbon Electrode |
title_full | Reagentless Amperometric Pyruvate Biosensor Based
on a Prussian Blue- and Enzyme Nanoparticle-Modified Screen-Printed
Carbon Electrode |
title_fullStr | Reagentless Amperometric Pyruvate Biosensor Based
on a Prussian Blue- and Enzyme Nanoparticle-Modified Screen-Printed
Carbon Electrode |
title_full_unstemmed | Reagentless Amperometric Pyruvate Biosensor Based
on a Prussian Blue- and Enzyme Nanoparticle-Modified Screen-Printed
Carbon Electrode |
title_short | Reagentless Amperometric Pyruvate Biosensor Based
on a Prussian Blue- and Enzyme Nanoparticle-Modified Screen-Printed
Carbon Electrode |
title_sort | reagentless amperometric pyruvate biosensor based
on a prussian blue- and enzyme nanoparticle-modified screen-printed
carbon electrode |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689939/ https://www.ncbi.nlm.nih.gov/pubmed/33251446 http://dx.doi.org/10.1021/acsomega.0c04522 |
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