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Non-equilibrium Inertial Separation Array for High-throughput, Large-volume Blood Fractionation
Microfluidic blood processing is used in a range of applications from cancer therapeutics to infectious disease diagnostics. As these applications are being translated to clinical use, processing larger volumes of blood in shorter timescales with high-reliability and robustness is becoming a pressin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5577162/ https://www.ncbi.nlm.nih.gov/pubmed/28855584 http://dx.doi.org/10.1038/s41598-017-10295-0 |
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author | Mutlu, Baris R. Smith, Kyle C. Edd, Jon F. Nadar, Priyanka Dlamini, Mcolisi Kapur, Ravi Toner, Mehmet |
author_facet | Mutlu, Baris R. Smith, Kyle C. Edd, Jon F. Nadar, Priyanka Dlamini, Mcolisi Kapur, Ravi Toner, Mehmet |
author_sort | Mutlu, Baris R. |
collection | PubMed |
description | Microfluidic blood processing is used in a range of applications from cancer therapeutics to infectious disease diagnostics. As these applications are being translated to clinical use, processing larger volumes of blood in shorter timescales with high-reliability and robustness is becoming a pressing need. In this work, we report a scaled, label-free cell separation mechanism called non-equilibrium inertial separation array (NISA). The NISA mechanism consists of an array of islands that exert a passive inertial lift force on proximate cells, thus enabling gentler manipulation of the cells without the need of physical contact. As the cells follow their size-based, deterministic path to their equilibrium positions, a preset fraction of the flow is siphoned to separate the smaller cells from the main flow. The NISA device was used to fractionate 400 mL of whole blood in less than 3 hours, and produce an ultrapure buffy coat (96.6% white blood cell yield, 0.0059% red blood cell carryover) by processing whole blood at 3 mL/min, or ∼300 million cells/second. This device presents a feasible alternative for fractionating blood for transfusion, cellular therapy and blood-based diagnostics, and could significantly improve the sensitivity of rare cell isolation devices by increasing the processed whole blood volume. |
format | Online Article Text |
id | pubmed-5577162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55771622017-09-01 Non-equilibrium Inertial Separation Array for High-throughput, Large-volume Blood Fractionation Mutlu, Baris R. Smith, Kyle C. Edd, Jon F. Nadar, Priyanka Dlamini, Mcolisi Kapur, Ravi Toner, Mehmet Sci Rep Article Microfluidic blood processing is used in a range of applications from cancer therapeutics to infectious disease diagnostics. As these applications are being translated to clinical use, processing larger volumes of blood in shorter timescales with high-reliability and robustness is becoming a pressing need. In this work, we report a scaled, label-free cell separation mechanism called non-equilibrium inertial separation array (NISA). The NISA mechanism consists of an array of islands that exert a passive inertial lift force on proximate cells, thus enabling gentler manipulation of the cells without the need of physical contact. As the cells follow their size-based, deterministic path to their equilibrium positions, a preset fraction of the flow is siphoned to separate the smaller cells from the main flow. The NISA device was used to fractionate 400 mL of whole blood in less than 3 hours, and produce an ultrapure buffy coat (96.6% white blood cell yield, 0.0059% red blood cell carryover) by processing whole blood at 3 mL/min, or ∼300 million cells/second. This device presents a feasible alternative for fractionating blood for transfusion, cellular therapy and blood-based diagnostics, and could significantly improve the sensitivity of rare cell isolation devices by increasing the processed whole blood volume. Nature Publishing Group UK 2017-08-30 /pmc/articles/PMC5577162/ /pubmed/28855584 http://dx.doi.org/10.1038/s41598-017-10295-0 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Mutlu, Baris R. Smith, Kyle C. Edd, Jon F. Nadar, Priyanka Dlamini, Mcolisi Kapur, Ravi Toner, Mehmet Non-equilibrium Inertial Separation Array for High-throughput, Large-volume Blood Fractionation |
title | Non-equilibrium Inertial Separation Array for High-throughput, Large-volume Blood Fractionation |
title_full | Non-equilibrium Inertial Separation Array for High-throughput, Large-volume Blood Fractionation |
title_fullStr | Non-equilibrium Inertial Separation Array for High-throughput, Large-volume Blood Fractionation |
title_full_unstemmed | Non-equilibrium Inertial Separation Array for High-throughput, Large-volume Blood Fractionation |
title_short | Non-equilibrium Inertial Separation Array for High-throughput, Large-volume Blood Fractionation |
title_sort | non-equilibrium inertial separation array for high-throughput, large-volume blood fractionation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5577162/ https://www.ncbi.nlm.nih.gov/pubmed/28855584 http://dx.doi.org/10.1038/s41598-017-10295-0 |
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