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Microfluidic Mixing and Analog On-Chip Concentration Control Using Fluidic Dielectrophoresis
Microfluidic platforms capable of complex on-chip processing and liquid handling enable a wide variety of sensing, cellular, and material-related applications across a spectrum of disciplines in engineering and biology. However, there is a general lack of available active microscale mixing methods c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6190360/ https://www.ncbi.nlm.nih.gov/pubmed/30404385 http://dx.doi.org/10.3390/mi7110214 |
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author | Mavrogiannis, Nicholas Desmond, Mitchell Ling, Kenny Fu, Xiaotong Gagnon, Zachary |
author_facet | Mavrogiannis, Nicholas Desmond, Mitchell Ling, Kenny Fu, Xiaotong Gagnon, Zachary |
author_sort | Mavrogiannis, Nicholas |
collection | PubMed |
description | Microfluidic platforms capable of complex on-chip processing and liquid handling enable a wide variety of sensing, cellular, and material-related applications across a spectrum of disciplines in engineering and biology. However, there is a general lack of available active microscale mixing methods capable of dynamically controlling on-chip solute concentrations in real-time. Hence, multiple microfluidic fluid handling steps are often needed for applications that require buffers at varying on-chip concentrations. Here, we present a novel electrokinetic method for actively mixing laminar fluids and controlling on-chip concentrations in microfluidic channels using fluidic dielectrophoresis. Using a microfluidic channel junction, we co-flow three electrolyte streams side-by-side so that two outer conductive streams enclose a low conductive central stream. The tri-laminar flow is driven through an array of electrodes where the outer streams are electrokinetically deflected and forced to mix with the central flow field. This newly mixed central flow is then sent continuously downstream to serve as a concentration boundary condition for a microfluidic gradient chamber. We demonstrate that by actively mixing the upstream fluids, a variable concentration gradient can be formed dynamically downstream with single a fixed inlet concentration. This novel mixing approach offers a useful method for producing variable on-chip concentrations from a single inlet source. |
format | Online Article Text |
id | pubmed-6190360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61903602018-11-01 Microfluidic Mixing and Analog On-Chip Concentration Control Using Fluidic Dielectrophoresis Mavrogiannis, Nicholas Desmond, Mitchell Ling, Kenny Fu, Xiaotong Gagnon, Zachary Micromachines (Basel) Article Microfluidic platforms capable of complex on-chip processing and liquid handling enable a wide variety of sensing, cellular, and material-related applications across a spectrum of disciplines in engineering and biology. However, there is a general lack of available active microscale mixing methods capable of dynamically controlling on-chip solute concentrations in real-time. Hence, multiple microfluidic fluid handling steps are often needed for applications that require buffers at varying on-chip concentrations. Here, we present a novel electrokinetic method for actively mixing laminar fluids and controlling on-chip concentrations in microfluidic channels using fluidic dielectrophoresis. Using a microfluidic channel junction, we co-flow three electrolyte streams side-by-side so that two outer conductive streams enclose a low conductive central stream. The tri-laminar flow is driven through an array of electrodes where the outer streams are electrokinetically deflected and forced to mix with the central flow field. This newly mixed central flow is then sent continuously downstream to serve as a concentration boundary condition for a microfluidic gradient chamber. We demonstrate that by actively mixing the upstream fluids, a variable concentration gradient can be formed dynamically downstream with single a fixed inlet concentration. This novel mixing approach offers a useful method for producing variable on-chip concentrations from a single inlet source. MDPI 2016-11-23 /pmc/articles/PMC6190360/ /pubmed/30404385 http://dx.doi.org/10.3390/mi7110214 Text en © 2016 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 Mavrogiannis, Nicholas Desmond, Mitchell Ling, Kenny Fu, Xiaotong Gagnon, Zachary Microfluidic Mixing and Analog On-Chip Concentration Control Using Fluidic Dielectrophoresis |
title | Microfluidic Mixing and Analog On-Chip Concentration Control Using Fluidic Dielectrophoresis |
title_full | Microfluidic Mixing and Analog On-Chip Concentration Control Using Fluidic Dielectrophoresis |
title_fullStr | Microfluidic Mixing and Analog On-Chip Concentration Control Using Fluidic Dielectrophoresis |
title_full_unstemmed | Microfluidic Mixing and Analog On-Chip Concentration Control Using Fluidic Dielectrophoresis |
title_short | Microfluidic Mixing and Analog On-Chip Concentration Control Using Fluidic Dielectrophoresis |
title_sort | microfluidic mixing and analog on-chip concentration control using fluidic dielectrophoresis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6190360/ https://www.ncbi.nlm.nih.gov/pubmed/30404385 http://dx.doi.org/10.3390/mi7110214 |
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