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Article: Reversibly-bonded microfluidic devices for stable cell culture and rapid, gentle cell extraction

TitleReversibly-bonded microfluidic devices for stable cell culture and rapid, gentle cell extraction
Authors
Issue Date20-Jul-2024
PublisherRoyal Society of Chemistry
Citation
Lab on a Chip, 2024, v. 24, n. 14, p. 3546-3555 How to Cite?
Abstract

Microfluidic chips have emerged as significant tools in cell culture due to their capacity for supporting cells to adopt more physiologically relevant morphologies in 3D compared with traditional cell culture in 2D. Currently, irreversible bonding methods, where chips cannot be detached from their substrates without destroying the structure, are commonly used in fabrication, making it challenging to conduct further analysis on cells that have been cultured on-chip. Although some reversible bonding techniques have been developed, they are either restricted to certain materials such as glass, or require complex processing procedures. Here, we demonstrate a simple and reversible polydimethylsiloxane (PDMS)–polystyrene (PS) bonding technique that allows devices to withstand extended operations while pressurized, and supports long-term stable cell cultures. More importantly, it allows rapid and gentle live cell extraction for downstream manipulation and characterization after long-term on-chip culturing, and even further subculturing. Our new approach could greatly facilitate microfluidic chip-based cell and tissue cultures, overcoming current analytical limitations and opening up new avenues for downstream uses of on-chip cultures, including 3D-engineered tissue structures for biomedical applications.


Persistent Identifierhttp://hdl.handle.net/10722/344780
ISSN
2023 Impact Factor: 6.1
2023 SCImago Journal Rankings: 1.246

 

DC FieldValueLanguage
dc.contributor.authorFeng, Xiaohan-
dc.contributor.authorWu, Zehaoyu-
dc.contributor.authorCheng, Lily Kwan Wai-
dc.contributor.authorXiang, Yang-
dc.contributor.authorSugimura, Ryohichi-
dc.contributor.authorLin, Xuyan-
dc.contributor.authorWu, Angela Ruohao-
dc.date.accessioned2024-08-12T04:07:22Z-
dc.date.available2024-08-12T04:07:22Z-
dc.date.issued2024-07-20-
dc.identifier.citationLab on a Chip, 2024, v. 24, n. 14, p. 3546-3555-
dc.identifier.issn1473-0197-
dc.identifier.urihttp://hdl.handle.net/10722/344780-
dc.description.abstract<p>Microfluidic chips have emerged as significant tools in cell culture due to their capacity for supporting cells to adopt more physiologically relevant morphologies in 3D compared with traditional cell culture in 2D. Currently, irreversible bonding methods, where chips cannot be detached from their substrates without destroying the structure, are commonly used in fabrication, making it challenging to conduct further analysis on cells that have been cultured on-chip. Although some reversible bonding techniques have been developed, they are either restricted to certain materials such as glass, or require complex processing procedures. Here, we demonstrate a simple and reversible polydimethylsiloxane (PDMS)–polystyrene (PS) bonding technique that allows devices to withstand extended operations while pressurized, and supports long-term stable cell cultures. More importantly, it allows rapid and gentle live cell extraction for downstream manipulation and characterization after long-term on-chip culturing, and even further subculturing. Our new approach could greatly facilitate microfluidic chip-based cell and tissue cultures, overcoming current analytical limitations and opening up new avenues for downstream uses of on-chip cultures, including 3D-engineered tissue structures for biomedical applications.<br></p>-
dc.languageeng-
dc.publisherRoyal Society of Chemistry-
dc.relation.ispartofLab on a Chip-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleReversibly-bonded microfluidic devices for stable cell culture and rapid, gentle cell extraction-
dc.typeArticle-
dc.identifier.doi10.1039/D3LC01019H-
dc.identifier.scopuseid_2-s2.0-85197399298-
dc.identifier.volume24-
dc.identifier.issue14-
dc.identifier.spage3546-
dc.identifier.epage3555-
dc.identifier.eissn1473-0189-
dc.identifier.issnl1473-0189-

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