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Characterization of a Centrifugal Microfluidic Orthogonal Flow Platform
To bring to bear the power of centrifugal microfluidics on vertical flow immunoassays, control of flow orthogonally through nanoporous membranes is essential. The on-disc approach described here leverages the rapid print-cut-laminate (PCL) disc fabrication and prototyping method to create a permanen...
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/PMC8950265/ https://www.ncbi.nlm.nih.gov/pubmed/35334778 http://dx.doi.org/10.3390/mi13030487 |
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author | Woolf, Michael Shane Dignan, Leah M. Karas, Scott M. Lewis, Hannah M. Hadley, Kevyn C. Nauman, Aeren Q. Gates-Hollingsworth, Marcellene A. AuCoin, David P. Green, Heather R. Geise, Geoffrey M. Landers, James P. |
author_facet | Woolf, Michael Shane Dignan, Leah M. Karas, Scott M. Lewis, Hannah M. Hadley, Kevyn C. Nauman, Aeren Q. Gates-Hollingsworth, Marcellene A. AuCoin, David P. Green, Heather R. Geise, Geoffrey M. Landers, James P. |
author_sort | Woolf, Michael Shane |
collection | PubMed |
description | To bring to bear the power of centrifugal microfluidics on vertical flow immunoassays, control of flow orthogonally through nanoporous membranes is essential. The on-disc approach described here leverages the rapid print-cut-laminate (PCL) disc fabrication and prototyping method to create a permanent seal between disc materials and embedded nanoporous membranes. Rotational forces drive fluid flow, replacing capillary action, and complex pneumatic pumping systems. Adjacent microfluidic features form a flow path that directs fluid orthogonally (vertically) through these embedded membranes during assay execution. This method for membrane incorporation circumvents the need for solvents (e.g., acetone) to create the membrane-disc bond and sidesteps issues related to undesirable bypass flow. In other recently published work, we described an orthogonal flow (OF) platform that exploited embedded membranes for automation of enzyme-linked immunosorbent assays (ELISAs). Here, we more fully characterize flow patterns and cellulosic membrane behavior within the centrifugal orthogonal flow (cOF) format. Specifically, high-speed videography studies demonstrate that sample volume, membrane pore size, and ionic composition of the sample matrix significantly impact membrane behavior, and consequently fluid drainage profiles, especially when cellulosic membranes are used. Finally, prototype discs are used to demonstrate proof-of-principle for sandwich-type antigen capture and immunodetection within the cOF system. |
format | Online Article Text |
id | pubmed-8950265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89502652022-03-26 Characterization of a Centrifugal Microfluidic Orthogonal Flow Platform Woolf, Michael Shane Dignan, Leah M. Karas, Scott M. Lewis, Hannah M. Hadley, Kevyn C. Nauman, Aeren Q. Gates-Hollingsworth, Marcellene A. AuCoin, David P. Green, Heather R. Geise, Geoffrey M. Landers, James P. Micromachines (Basel) Article To bring to bear the power of centrifugal microfluidics on vertical flow immunoassays, control of flow orthogonally through nanoporous membranes is essential. The on-disc approach described here leverages the rapid print-cut-laminate (PCL) disc fabrication and prototyping method to create a permanent seal between disc materials and embedded nanoporous membranes. Rotational forces drive fluid flow, replacing capillary action, and complex pneumatic pumping systems. Adjacent microfluidic features form a flow path that directs fluid orthogonally (vertically) through these embedded membranes during assay execution. This method for membrane incorporation circumvents the need for solvents (e.g., acetone) to create the membrane-disc bond and sidesteps issues related to undesirable bypass flow. In other recently published work, we described an orthogonal flow (OF) platform that exploited embedded membranes for automation of enzyme-linked immunosorbent assays (ELISAs). Here, we more fully characterize flow patterns and cellulosic membrane behavior within the centrifugal orthogonal flow (cOF) format. Specifically, high-speed videography studies demonstrate that sample volume, membrane pore size, and ionic composition of the sample matrix significantly impact membrane behavior, and consequently fluid drainage profiles, especially when cellulosic membranes are used. Finally, prototype discs are used to demonstrate proof-of-principle for sandwich-type antigen capture and immunodetection within the cOF system. MDPI 2022-03-20 /pmc/articles/PMC8950265/ /pubmed/35334778 http://dx.doi.org/10.3390/mi13030487 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 Woolf, Michael Shane Dignan, Leah M. Karas, Scott M. Lewis, Hannah M. Hadley, Kevyn C. Nauman, Aeren Q. Gates-Hollingsworth, Marcellene A. AuCoin, David P. Green, Heather R. Geise, Geoffrey M. Landers, James P. Characterization of a Centrifugal Microfluidic Orthogonal Flow Platform |
title | Characterization of a Centrifugal Microfluidic Orthogonal Flow Platform |
title_full | Characterization of a Centrifugal Microfluidic Orthogonal Flow Platform |
title_fullStr | Characterization of a Centrifugal Microfluidic Orthogonal Flow Platform |
title_full_unstemmed | Characterization of a Centrifugal Microfluidic Orthogonal Flow Platform |
title_short | Characterization of a Centrifugal Microfluidic Orthogonal Flow Platform |
title_sort | characterization of a centrifugal microfluidic orthogonal flow platform |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8950265/ https://www.ncbi.nlm.nih.gov/pubmed/35334778 http://dx.doi.org/10.3390/mi13030487 |
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