High-Throughput, Label-Free Isolation of White Blood Cells from Whole Blood Using Parallel Spiral Microchannels with U-Shaped Cross-Section

Rapid isolation of white blood cells (WBCs) from whole blood is an essential part of any WBC examination platform. However, most conventional cell separation techniques are labor-intensive and low throughput, require large volumes of samples, need extensive cell manipulation, and have low purity. To...

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Autores principales: Amirhossein Mehran, Peyman Rostami, Mohammad Said Saidi, Bahar Firoozabadi, Navid Kashaninejad
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Lenguaje:EN
Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:5081587b52fe4e3f8a63d86d5c4880f72021-11-25T16:54:48ZHigh-Throughput, Label-Free Isolation of White Blood Cells from Whole Blood Using Parallel Spiral Microchannels with U-Shaped Cross-Section10.3390/bios111104062079-6374https://doaj.org/article/5081587b52fe4e3f8a63d86d5c4880f72021-10-01T00:00:00Zhttps://www.mdpi.com/2079-6374/11/11/406https://doaj.org/toc/2079-6374Rapid isolation of white blood cells (WBCs) from whole blood is an essential part of any WBC examination platform. However, most conventional cell separation techniques are labor-intensive and low throughput, require large volumes of samples, need extensive cell manipulation, and have low purity. To address these challenges, we report the design and fabrication of a passive, label-free microfluidic device with a unique U-shaped cross-section to separate WBCs from whole blood using hydrodynamic forces that exist in a microchannel with curvilinear geometry. It is shown that the spiral microchannel with a U-shaped cross-section concentrates larger blood cells (e.g., WBCs) in the inner cross-section of the microchannel by moving smaller blood cells (e.g., RBCs and platelets) to the outer microchannel section and preventing them from returning to the inner microchannel section. Therefore, it overcomes the major limitation of a rectangular cross-section where secondary Dean vortices constantly enforce particles throughout the entire cross-section and decrease its isolation efficiency. Under optimal settings, we managed to isolate more than 95% of WBCs from whole blood under high-throughput (6 mL/min), high-purity (88%), and high-capacity (360 mL of sample in 1 h) conditions. High efficiency, fast processing time, and non-invasive WBC isolation from large blood samples without centrifugation, RBC lysis, cell biomarkers, and chemical pre-treatments make this method an ideal choice for downstream cell study platforms.Amirhossein MehranPeyman RostamiMohammad Said SaidiBahar FiroozabadiNavid KashaninejadMDPI AGarticleWBC isolationspiral microchannelsinertial microfluidicspassive cell separationhigh-throughput separationBiotechnologyTP248.13-248.65ENBiosensors, Vol 11, Iss 406, p 406 (2021)
institution DOAJ
collection DOAJ
language EN
topic WBC isolation
spiral microchannels
inertial microfluidics
passive cell separation
high-throughput separation
Biotechnology
TP248.13-248.65
spellingShingle WBC isolation
spiral microchannels
inertial microfluidics
passive cell separation
high-throughput separation
Biotechnology
TP248.13-248.65
Amirhossein Mehran
Peyman Rostami
Mohammad Said Saidi
Bahar Firoozabadi
Navid Kashaninejad
High-Throughput, Label-Free Isolation of White Blood Cells from Whole Blood Using Parallel Spiral Microchannels with U-Shaped Cross-Section
description Rapid isolation of white blood cells (WBCs) from whole blood is an essential part of any WBC examination platform. However, most conventional cell separation techniques are labor-intensive and low throughput, require large volumes of samples, need extensive cell manipulation, and have low purity. To address these challenges, we report the design and fabrication of a passive, label-free microfluidic device with a unique U-shaped cross-section to separate WBCs from whole blood using hydrodynamic forces that exist in a microchannel with curvilinear geometry. It is shown that the spiral microchannel with a U-shaped cross-section concentrates larger blood cells (e.g., WBCs) in the inner cross-section of the microchannel by moving smaller blood cells (e.g., RBCs and platelets) to the outer microchannel section and preventing them from returning to the inner microchannel section. Therefore, it overcomes the major limitation of a rectangular cross-section where secondary Dean vortices constantly enforce particles throughout the entire cross-section and decrease its isolation efficiency. Under optimal settings, we managed to isolate more than 95% of WBCs from whole blood under high-throughput (6 mL/min), high-purity (88%), and high-capacity (360 mL of sample in 1 h) conditions. High efficiency, fast processing time, and non-invasive WBC isolation from large blood samples without centrifugation, RBC lysis, cell biomarkers, and chemical pre-treatments make this method an ideal choice for downstream cell study platforms.
format article
author Amirhossein Mehran
Peyman Rostami
Mohammad Said Saidi
Bahar Firoozabadi
Navid Kashaninejad
author_facet Amirhossein Mehran
Peyman Rostami
Mohammad Said Saidi
Bahar Firoozabadi
Navid Kashaninejad
author_sort Amirhossein Mehran
title High-Throughput, Label-Free Isolation of White Blood Cells from Whole Blood Using Parallel Spiral Microchannels with U-Shaped Cross-Section
title_short High-Throughput, Label-Free Isolation of White Blood Cells from Whole Blood Using Parallel Spiral Microchannels with U-Shaped Cross-Section
title_full High-Throughput, Label-Free Isolation of White Blood Cells from Whole Blood Using Parallel Spiral Microchannels with U-Shaped Cross-Section
title_fullStr High-Throughput, Label-Free Isolation of White Blood Cells from Whole Blood Using Parallel Spiral Microchannels with U-Shaped Cross-Section
title_full_unstemmed High-Throughput, Label-Free Isolation of White Blood Cells from Whole Blood Using Parallel Spiral Microchannels with U-Shaped Cross-Section
title_sort high-throughput, label-free isolation of white blood cells from whole blood using parallel spiral microchannels with u-shaped cross-section
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/5081587b52fe4e3f8a63d86d5c4880f7
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