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A Novel Microfluidic Point-of-Care Biosensor System on Printed Circuit Board for Cytokine Detection
Point of Care (PoC) diagnostics have been the subject of considerable research over the last few decades driven by the pressure to detect diseases quickly and effectively and reduce healthcare costs. Herein, we demonstrate a novel, fully integrated, microfluidic amperometric enzyme-linked immunosorb...
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/PMC6264023/ https://www.ncbi.nlm.nih.gov/pubmed/30453609 http://dx.doi.org/10.3390/s18114011 |
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author | Evans, Daniel Papadimitriou, Konstantinos I. Vasilakis, Nikolaos Pantelidis, Panagiotis Kelleher, Peter Morgan, Hywel Prodromakis, Themistoklis |
author_facet | Evans, Daniel Papadimitriou, Konstantinos I. Vasilakis, Nikolaos Pantelidis, Panagiotis Kelleher, Peter Morgan, Hywel Prodromakis, Themistoklis |
author_sort | Evans, Daniel |
collection | PubMed |
description | Point of Care (PoC) diagnostics have been the subject of considerable research over the last few decades driven by the pressure to detect diseases quickly and effectively and reduce healthcare costs. Herein, we demonstrate a novel, fully integrated, microfluidic amperometric enzyme-linked immunosorbent assay (ELISA) prototype using a commercial interferon gamma release assay (IGRA) as a model antibody binding system. Microfluidic assay chemistry was engineered to take place on Au-plated electrodes within an assay cell on a printed circuit board (PCB)-based biosensor system. The assay cell is linked to an electrochemical reporter cell comprising microfluidic architecture, Au working and counter electrodes and a Ag/AgCl reference electrode, all manufactured exclusively via standard commercial PCB fabrication processes. Assay chemistry has been optimised for microfluidic diffusion kinetics to function under continual flow. We characterised the electrode integrity of the developed platforms with reference to biological sampling and buffer composition and subsequently we demonstrated concentration-dependent measurements of H(2)O(2) depletion as resolved by existing FDA-validated ELISA kits. Finally, we validated the assay technology in both buffer and serum and demonstrate limits of detection comparable to high-end commercial systems with the addition of full microfluidic assay architecture capable of returning diagnostic analyses in approximately eight minutes. |
format | Online Article Text |
id | pubmed-6264023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62640232018-12-12 A Novel Microfluidic Point-of-Care Biosensor System on Printed Circuit Board for Cytokine Detection Evans, Daniel Papadimitriou, Konstantinos I. Vasilakis, Nikolaos Pantelidis, Panagiotis Kelleher, Peter Morgan, Hywel Prodromakis, Themistoklis Sensors (Basel) Article Point of Care (PoC) diagnostics have been the subject of considerable research over the last few decades driven by the pressure to detect diseases quickly and effectively and reduce healthcare costs. Herein, we demonstrate a novel, fully integrated, microfluidic amperometric enzyme-linked immunosorbent assay (ELISA) prototype using a commercial interferon gamma release assay (IGRA) as a model antibody binding system. Microfluidic assay chemistry was engineered to take place on Au-plated electrodes within an assay cell on a printed circuit board (PCB)-based biosensor system. The assay cell is linked to an electrochemical reporter cell comprising microfluidic architecture, Au working and counter electrodes and a Ag/AgCl reference electrode, all manufactured exclusively via standard commercial PCB fabrication processes. Assay chemistry has been optimised for microfluidic diffusion kinetics to function under continual flow. We characterised the electrode integrity of the developed platforms with reference to biological sampling and buffer composition and subsequently we demonstrated concentration-dependent measurements of H(2)O(2) depletion as resolved by existing FDA-validated ELISA kits. Finally, we validated the assay technology in both buffer and serum and demonstrate limits of detection comparable to high-end commercial systems with the addition of full microfluidic assay architecture capable of returning diagnostic analyses in approximately eight minutes. MDPI 2018-11-17 /pmc/articles/PMC6264023/ /pubmed/30453609 http://dx.doi.org/10.3390/s18114011 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 Evans, Daniel Papadimitriou, Konstantinos I. Vasilakis, Nikolaos Pantelidis, Panagiotis Kelleher, Peter Morgan, Hywel Prodromakis, Themistoklis A Novel Microfluidic Point-of-Care Biosensor System on Printed Circuit Board for Cytokine Detection |
title | A Novel Microfluidic Point-of-Care Biosensor System on Printed Circuit Board for Cytokine Detection |
title_full | A Novel Microfluidic Point-of-Care Biosensor System on Printed Circuit Board for Cytokine Detection |
title_fullStr | A Novel Microfluidic Point-of-Care Biosensor System on Printed Circuit Board for Cytokine Detection |
title_full_unstemmed | A Novel Microfluidic Point-of-Care Biosensor System on Printed Circuit Board for Cytokine Detection |
title_short | A Novel Microfluidic Point-of-Care Biosensor System on Printed Circuit Board for Cytokine Detection |
title_sort | novel microfluidic point-of-care biosensor system on printed circuit board for cytokine detection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264023/ https://www.ncbi.nlm.nih.gov/pubmed/30453609 http://dx.doi.org/10.3390/s18114011 |
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