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Generation of Dynamic Concentration Profile Using A Microfluidic Device Integrating Pneumatic Microvalves
Generating and maintaining the concentration dilutions of diffusible molecules in microchannels is critical for high-throughput chemical and biological analysis. Conventional serial network microfluidic technologies can generate high orders of arbitrary concentrations by a predefined microchannel ne...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599525/ https://www.ncbi.nlm.nih.gov/pubmed/36291005 http://dx.doi.org/10.3390/bios12100868 |
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author | Chen, Chang Li, Panpan Guo, Tianruo Chen, Siyuan Xu, Dong Chen, Huaying |
author_facet | Chen, Chang Li, Panpan Guo, Tianruo Chen, Siyuan Xu, Dong Chen, Huaying |
author_sort | Chen, Chang |
collection | PubMed |
description | Generating and maintaining the concentration dilutions of diffusible molecules in microchannels is critical for high-throughput chemical and biological analysis. Conventional serial network microfluidic technologies can generate high orders of arbitrary concentrations by a predefined microchannel network. However, a previous design requires a large occupancy area and is unable to dynamically generate different profiles in the same chip, limiting its applications. This study developed a microfluidic device enabling dynamic variations of both the concentration in the same channel and the concentration distribution in multiple channels by adjusting the flow resistance using programmable pneumatic microvalves. The key component (the pneumatic microvalve) allowed dynamic adjustment of the concentration profile but occupied a tiny space. Additionally, a Matlab program was developed to calculate the flow rates and flow resistance of various sections of the device, which provided theoretical guidance for dimension design. In silico investigations were conducted to evaluate the microvalve deformation with widths from 100 to 300 µm and membrane thicknesses of 20 and 30 µm under the activation pressures between 0 and 2000 mbar. The flow resistance of the deformed valve was studied both numerically and experimentally and an empirical model for valve flow resistance with the form of [Formula: see text] was proposed. Afterward, the fluid flow in the valve region was characterized using Micro PIV to further demonstrate the adjustment mechanism of the flow resistance. Then, the herringbone structures were employed for fast mixing to allow both quick variation of concentration and minor space usage of the channel network. Finally, an empirical formula-supported computational program was developed to provide the activation pressures required for the specific concentration profile. Both linear ([Formula: see text] = −0.2k + 1) and nonlinear [Formula: see text] = [Formula: see text] concentration distribution in four channels were varied using the same device by adjusting microvalves. The device demonstrated the capability to control the concentration profile dynamically in a small space, offering superior application potentials in analytical chemistry, drug screening, and cell biology research. |
format | Online Article Text |
id | pubmed-9599525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95995252022-10-27 Generation of Dynamic Concentration Profile Using A Microfluidic Device Integrating Pneumatic Microvalves Chen, Chang Li, Panpan Guo, Tianruo Chen, Siyuan Xu, Dong Chen, Huaying Biosensors (Basel) Article Generating and maintaining the concentration dilutions of diffusible molecules in microchannels is critical for high-throughput chemical and biological analysis. Conventional serial network microfluidic technologies can generate high orders of arbitrary concentrations by a predefined microchannel network. However, a previous design requires a large occupancy area and is unable to dynamically generate different profiles in the same chip, limiting its applications. This study developed a microfluidic device enabling dynamic variations of both the concentration in the same channel and the concentration distribution in multiple channels by adjusting the flow resistance using programmable pneumatic microvalves. The key component (the pneumatic microvalve) allowed dynamic adjustment of the concentration profile but occupied a tiny space. Additionally, a Matlab program was developed to calculate the flow rates and flow resistance of various sections of the device, which provided theoretical guidance for dimension design. In silico investigations were conducted to evaluate the microvalve deformation with widths from 100 to 300 µm and membrane thicknesses of 20 and 30 µm under the activation pressures between 0 and 2000 mbar. The flow resistance of the deformed valve was studied both numerically and experimentally and an empirical model for valve flow resistance with the form of [Formula: see text] was proposed. Afterward, the fluid flow in the valve region was characterized using Micro PIV to further demonstrate the adjustment mechanism of the flow resistance. Then, the herringbone structures were employed for fast mixing to allow both quick variation of concentration and minor space usage of the channel network. Finally, an empirical formula-supported computational program was developed to provide the activation pressures required for the specific concentration profile. Both linear ([Formula: see text] = −0.2k + 1) and nonlinear [Formula: see text] = [Formula: see text] concentration distribution in four channels were varied using the same device by adjusting microvalves. The device demonstrated the capability to control the concentration profile dynamically in a small space, offering superior application potentials in analytical chemistry, drug screening, and cell biology research. MDPI 2022-10-13 /pmc/articles/PMC9599525/ /pubmed/36291005 http://dx.doi.org/10.3390/bios12100868 Text en © 2022 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 Chen, Chang Li, Panpan Guo, Tianruo Chen, Siyuan Xu, Dong Chen, Huaying Generation of Dynamic Concentration Profile Using A Microfluidic Device Integrating Pneumatic Microvalves |
title | Generation of Dynamic Concentration Profile Using A Microfluidic Device Integrating Pneumatic Microvalves |
title_full | Generation of Dynamic Concentration Profile Using A Microfluidic Device Integrating Pneumatic Microvalves |
title_fullStr | Generation of Dynamic Concentration Profile Using A Microfluidic Device Integrating Pneumatic Microvalves |
title_full_unstemmed | Generation of Dynamic Concentration Profile Using A Microfluidic Device Integrating Pneumatic Microvalves |
title_short | Generation of Dynamic Concentration Profile Using A Microfluidic Device Integrating Pneumatic Microvalves |
title_sort | generation of dynamic concentration profile using a microfluidic device integrating pneumatic microvalves |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599525/ https://www.ncbi.nlm.nih.gov/pubmed/36291005 http://dx.doi.org/10.3390/bios12100868 |
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