Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/174970
Title: Enhancing single-cell encapsulation in droplet microfluidics with fine-tunable on-chip sample enrichment
Authors: Tang, Tao
Zhao, Hao
Shen, Shaofei
Yang, Like
Lim, Chwee Teck
Keywords: Engineering
Issue Date: 2024
Source: 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
Journal: Microsystems & Nanoengineering 
Abstract: 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.
URI: https://hdl.handle.net/10356/174970
ISSN: 2055-7434
DOI: 10.1038/s41378-023-00631-y
Organisations: Department of Biomedical Engineering, NUS 
NUS Graduate School 
Institute for Health Innovation & Technology, NUS 
Mechanobiology Institute, NUS 
Research Centres: Institute for Digital Molecular Analytics and Science (IDMxS)
Rights: © 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/.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:IDMxS Journal Articles

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