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Isothermal Recombinase Polymerase Amplification (RPA) of E. coli gDNA in Commercially Fabricated PCB-Based Microfluidic Platforms
Printed circuit board (PCB) technology has been recently proposed as a convenient platform for seamlessly integrating electronics and microfluidics in the same substrate, thus facilitating the introduction of integrated and low-cost microfluidic devices to the market, thanks to the inherent upscalin...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8619769/ https://www.ncbi.nlm.nih.gov/pubmed/34832799 http://dx.doi.org/10.3390/mi12111387 |
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author | Georgoutsou-Spyridonos, Maria Filippidou, Myrto Kaprou, Georgia D. Mastellos, Dimitrios C. Chatzandroulis, Stavros Tserepi, Angeliki |
author_facet | Georgoutsou-Spyridonos, Maria Filippidou, Myrto Kaprou, Georgia D. Mastellos, Dimitrios C. Chatzandroulis, Stavros Tserepi, Angeliki |
author_sort | Georgoutsou-Spyridonos, Maria |
collection | PubMed |
description | Printed circuit board (PCB) technology has been recently proposed as a convenient platform for seamlessly integrating electronics and microfluidics in the same substrate, thus facilitating the introduction of integrated and low-cost microfluidic devices to the market, thanks to the inherent upscaling potential of the PCB industry. Herein, a microfluidic chip, encompassing on PCB both a meandering microchannel and microheaters to accommodate recombinase polymerase amplification (RPA), is designed and commercially fabricated for the first time on PCB. The developed microchip is validated for RPA-based amplification of two E. coli target genes compared to a conventional thermocycler. The RPA performance of the PCB microchip was found to be well-comparable to that of a thermocycler yet with a remarkably lower power consumption (0.6 W). This microchip is intended for seamless integration with biosensors in the same PCB substrate for the development of a point-of-care (POC) molecular diagnostics platform. |
format | Online Article Text |
id | pubmed-8619769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86197692021-11-27 Isothermal Recombinase Polymerase Amplification (RPA) of E. coli gDNA in Commercially Fabricated PCB-Based Microfluidic Platforms Georgoutsou-Spyridonos, Maria Filippidou, Myrto Kaprou, Georgia D. Mastellos, Dimitrios C. Chatzandroulis, Stavros Tserepi, Angeliki Micromachines (Basel) Article Printed circuit board (PCB) technology has been recently proposed as a convenient platform for seamlessly integrating electronics and microfluidics in the same substrate, thus facilitating the introduction of integrated and low-cost microfluidic devices to the market, thanks to the inherent upscaling potential of the PCB industry. Herein, a microfluidic chip, encompassing on PCB both a meandering microchannel and microheaters to accommodate recombinase polymerase amplification (RPA), is designed and commercially fabricated for the first time on PCB. The developed microchip is validated for RPA-based amplification of two E. coli target genes compared to a conventional thermocycler. The RPA performance of the PCB microchip was found to be well-comparable to that of a thermocycler yet with a remarkably lower power consumption (0.6 W). This microchip is intended for seamless integration with biosensors in the same PCB substrate for the development of a point-of-care (POC) molecular diagnostics platform. MDPI 2021-11-12 /pmc/articles/PMC8619769/ /pubmed/34832799 http://dx.doi.org/10.3390/mi12111387 Text en © 2021 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 Georgoutsou-Spyridonos, Maria Filippidou, Myrto Kaprou, Georgia D. Mastellos, Dimitrios C. Chatzandroulis, Stavros Tserepi, Angeliki Isothermal Recombinase Polymerase Amplification (RPA) of E. coli gDNA in Commercially Fabricated PCB-Based Microfluidic Platforms |
title | Isothermal Recombinase Polymerase Amplification (RPA) of E. coli gDNA in Commercially Fabricated PCB-Based Microfluidic Platforms |
title_full | Isothermal Recombinase Polymerase Amplification (RPA) of E. coli gDNA in Commercially Fabricated PCB-Based Microfluidic Platforms |
title_fullStr | Isothermal Recombinase Polymerase Amplification (RPA) of E. coli gDNA in Commercially Fabricated PCB-Based Microfluidic Platforms |
title_full_unstemmed | Isothermal Recombinase Polymerase Amplification (RPA) of E. coli gDNA in Commercially Fabricated PCB-Based Microfluidic Platforms |
title_short | Isothermal Recombinase Polymerase Amplification (RPA) of E. coli gDNA in Commercially Fabricated PCB-Based Microfluidic Platforms |
title_sort | isothermal recombinase polymerase amplification (rpa) of e. coli gdna in commercially fabricated pcb-based microfluidic platforms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8619769/ https://www.ncbi.nlm.nih.gov/pubmed/34832799 http://dx.doi.org/10.3390/mi12111387 |
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