Enhancing single-cell encapsulation in droplet microfluidics with fine-tunable on-chip sample enrichment

Single-cell encapsulation in droplet microfluidics is commonly hindered by the tradeoff between cell suspension density and on-chip focusing performance. In this study, we introduce a novel droplet microfluidic chip to overcome this challenge. The chip comprises a double spiral focusing unit, a flow...

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Main Authors: Tang, Tao, Zhao, Hao, Shen, Shaofei, Yang, Like, Lim, Chwee Teck
Other Authors: Department of Biomedical Engineering, NUS
Format: Article
Language:English
Published: 2024
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Online Access:https://hdl.handle.net/10356/174970
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1749702024-04-17T15:32:23Z Enhancing single-cell encapsulation in droplet microfluidics with fine-tunable on-chip sample enrichment Tang, Tao Zhao, Hao Shen, Shaofei Yang, Like Lim, Chwee Teck Department of Biomedical Engineering, NUS NUS Graduate School Institute for Health Innovation & Technology, NUS Mechanobiology Institute, NUS Institute for Digital Molecular Analytics and Science (IDMxS) Engineering Cell Suspension Droplet microfluidics Single-cell encapsulation in droplet microfluidics is commonly hindered by the tradeoff between cell suspension density and on-chip focusing performance. In this study, we introduce a novel droplet microfluidic chip to overcome this challenge. The chip comprises a double spiral focusing unit, a flow resistance-based sample enrichment module with fine-tunable outlets, and a crossflow droplet generation unit. Utilizing a low-density cell/bead suspension (2 × 106 objects/mL), cells/beads are focused into a near-equidistant linear arrangement within the double spiral microchannel. The excess water phase is diverted while cells/beads remain focused and sequentially encapsulated in individual droplets. Focusing performance was assessed through numerical simulations and experiments at three flow rates (40, 60, 80 μL/min), demonstrating successful focusing at 40 and 80 μL/min for beads and cells, respectively. In addition, both simulation and experimental results revealed that the flow resistance at the sample enrichment module is adjustable by punching different outlets, allowing over 50% of the aqueous phase to be removed. YOLOv8n-based droplet detection algorithms realized the counting of cells/beads in droplets, statistically demonstrating single-cell and bead encapsulation rates of 72.2% and 79.2%, respectively. All the results indicate that this on-chip sample enrichment approach can be further developed and employed as a critical component in single-cell encapsulation in water-in-oil droplets. Nanyang Technological University Published version This work was supported by the Institute for Health Innovation and Technology (iHealthtech), Mechanobiology Institute and the MechanoBioEngineering Laboratory at the Department of Biomedical Engineering) at the National University of Singapore (NUS). We also acknowledge support from the Institute for Digital Molecular Analytics and Science at the Nanyang Technological University. 2024-04-17T07:13:13Z 2024-04-17T07:13:13Z 2024 Journal Article Tang, T., Zhao, H., Shen, S., Yang, L. & Lim, C. T. (2024). Enhancing single-cell encapsulation in droplet microfluidics with fine-tunable on-chip sample enrichment. Microsystems & Nanoengineering, 10(1), 3-. https://dx.doi.org/10.1038/s41378-023-00631-y 2055-7434 https://hdl.handle.net/10356/174970 10.1038/s41378-023-00631-y 38169721 2-s2.0-85180930069 1 10 3 en Microsystems & Nanoengineering © The Author(s) 2024. 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/. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering
Cell Suspension
Droplet microfluidics
spellingShingle Engineering
Cell Suspension
Droplet microfluidics
Tang, Tao
Zhao, Hao
Shen, Shaofei
Yang, Like
Lim, Chwee Teck
Enhancing single-cell encapsulation in droplet microfluidics with fine-tunable on-chip sample enrichment
description Single-cell encapsulation in droplet microfluidics is commonly hindered by the tradeoff between cell suspension density and on-chip focusing performance. In this study, we introduce a novel droplet microfluidic chip to overcome this challenge. The chip comprises a double spiral focusing unit, a flow resistance-based sample enrichment module with fine-tunable outlets, and a crossflow droplet generation unit. Utilizing a low-density cell/bead suspension (2 × 106 objects/mL), cells/beads are focused into a near-equidistant linear arrangement within the double spiral microchannel. The excess water phase is diverted while cells/beads remain focused and sequentially encapsulated in individual droplets. Focusing performance was assessed through numerical simulations and experiments at three flow rates (40, 60, 80 μL/min), demonstrating successful focusing at 40 and 80 μL/min for beads and cells, respectively. In addition, both simulation and experimental results revealed that the flow resistance at the sample enrichment module is adjustable by punching different outlets, allowing over 50% of the aqueous phase to be removed. YOLOv8n-based droplet detection algorithms realized the counting of cells/beads in droplets, statistically demonstrating single-cell and bead encapsulation rates of 72.2% and 79.2%, respectively. All the results indicate that this on-chip sample enrichment approach can be further developed and employed as a critical component in single-cell encapsulation in water-in-oil droplets.
author2 Department of Biomedical Engineering, NUS
author_facet Department of Biomedical Engineering, NUS
Tang, Tao
Zhao, Hao
Shen, Shaofei
Yang, Like
Lim, Chwee Teck
format Article
author Tang, Tao
Zhao, Hao
Shen, Shaofei
Yang, Like
Lim, Chwee Teck
author_sort Tang, Tao
title Enhancing single-cell encapsulation in droplet microfluidics with fine-tunable on-chip sample enrichment
title_short Enhancing single-cell encapsulation in droplet microfluidics with fine-tunable on-chip sample enrichment
title_full Enhancing single-cell encapsulation in droplet microfluidics with fine-tunable on-chip sample enrichment
title_fullStr Enhancing single-cell encapsulation in droplet microfluidics with fine-tunable on-chip sample enrichment
title_full_unstemmed Enhancing single-cell encapsulation in droplet microfluidics with fine-tunable on-chip sample enrichment
title_sort enhancing single-cell encapsulation in droplet microfluidics with fine-tunable on-chip sample enrichment
publishDate 2024
url https://hdl.handle.net/10356/174970
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