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Microfluidic deformability-activated sorting of single particles
Mechanical properties have emerged as a significant label-free marker for characterizing deformable particles such as cells. Here, we demonstrated the first single-particle-resolved, cytometry-like deformability-activated sorting in the continuous flow on a microfluidic chip. Compared with existing...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433438/ https://www.ncbi.nlm.nih.gov/pubmed/34567626 http://dx.doi.org/10.1038/s41378-019-0107-9 |
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author | Choi, Gihoon Nouri, Reza Zarzar, Lauren Guan, Weihua |
author_facet | Choi, Gihoon Nouri, Reza Zarzar, Lauren Guan, Weihua |
author_sort | Choi, Gihoon |
collection | PubMed |
description | Mechanical properties have emerged as a significant label-free marker for characterizing deformable particles such as cells. Here, we demonstrated the first single-particle-resolved, cytometry-like deformability-activated sorting in the continuous flow on a microfluidic chip. Compared with existing deformability-based sorting techniques, the microfluidic device presented in this work measures the deformability and immediately sorts the particles one-by-one in real time. It integrates the transit-time-based deformability measurement and active hydrodynamic sorting onto a single chip. We identified the critical factors that affect the sorting dynamics by modeling and experimental approaches. We found that the device throughput is determined by the summation of the sensing, buffering, and sorting time. A total time of ~100 ms is used for analyzing and sorting a single particle, leading to a throughput of 600 particles/min. We synthesized poly(ethylene glycol) diacrylate (PEGDA) hydrogel beads as the deformability model for device validation and performance evaluation. A deformability-activated sorting purity of 88% and an average efficiency of 73% were achieved. We anticipate that the ability to actively measure and sort individual particles one-by-one in a continuous flow would find applications in cell-mechanotyping studies such as correlational studies of the cell mechanical phenotype and molecular mechanism. |
format | Online Article Text |
id | pubmed-8433438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84334382021-09-24 Microfluidic deformability-activated sorting of single particles Choi, Gihoon Nouri, Reza Zarzar, Lauren Guan, Weihua Microsyst Nanoeng Article Mechanical properties have emerged as a significant label-free marker for characterizing deformable particles such as cells. Here, we demonstrated the first single-particle-resolved, cytometry-like deformability-activated sorting in the continuous flow on a microfluidic chip. Compared with existing deformability-based sorting techniques, the microfluidic device presented in this work measures the deformability and immediately sorts the particles one-by-one in real time. It integrates the transit-time-based deformability measurement and active hydrodynamic sorting onto a single chip. We identified the critical factors that affect the sorting dynamics by modeling and experimental approaches. We found that the device throughput is determined by the summation of the sensing, buffering, and sorting time. A total time of ~100 ms is used for analyzing and sorting a single particle, leading to a throughput of 600 particles/min. We synthesized poly(ethylene glycol) diacrylate (PEGDA) hydrogel beads as the deformability model for device validation and performance evaluation. A deformability-activated sorting purity of 88% and an average efficiency of 73% were achieved. We anticipate that the ability to actively measure and sort individual particles one-by-one in a continuous flow would find applications in cell-mechanotyping studies such as correlational studies of the cell mechanical phenotype and molecular mechanism. Nature Publishing Group UK 2020-02-10 /pmc/articles/PMC8433438/ /pubmed/34567626 http://dx.doi.org/10.1038/s41378-019-0107-9 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Choi, Gihoon Nouri, Reza Zarzar, Lauren Guan, Weihua Microfluidic deformability-activated sorting of single particles |
title | Microfluidic deformability-activated sorting of single particles |
title_full | Microfluidic deformability-activated sorting of single particles |
title_fullStr | Microfluidic deformability-activated sorting of single particles |
title_full_unstemmed | Microfluidic deformability-activated sorting of single particles |
title_short | Microfluidic deformability-activated sorting of single particles |
title_sort | microfluidic deformability-activated sorting of single particles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433438/ https://www.ncbi.nlm.nih.gov/pubmed/34567626 http://dx.doi.org/10.1038/s41378-019-0107-9 |
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