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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MDPI AG
2021
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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) |
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WBC isolation spiral microchannels inertial microfluidics passive cell separation high-throughput separation Biotechnology TP248.13-248.65 |
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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 |
work_keys_str_mv |
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