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Reversibly-bonded microfluidic devices for stable cell culture and rapid, gentle cell extraction.
Feng, Xiaohan; Wu, Zehaoyu; Cheng, Lily Kwan Wai; Xiang, Yang; Sugimura, Ryohichi; Lin, Xuyan; Wu, Angela Ruohao.
Affiliation
  • Feng X; Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong SAR. angelawu@ust.hk.
  • Wu Z; Division of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong SAR. xlinas@connect.ust.hk.
  • Cheng LKW; Division of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong SAR. xlinas@connect.ust.hk.
  • Xiang Y; Li Ka Shing Faculty of Medicine, School of Biomedical Sciences, University of Hong Kong, Hong Kong SAR, China.
  • Sugimura R; Li Ka Shing Faculty of Medicine, School of Biomedical Sciences, University of Hong Kong, Hong Kong SAR, China.
  • Lin X; Division of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong SAR. xlinas@connect.ust.hk.
  • Wu AR; Center for Engineering Material and Reliability, Guangzhou HKUST Fok Ying Tung Research Institute, Guangzhou, China.
Lab Chip ; 24(14): 3546-3555, 2024 Jul 10.
Article in En | MEDLINE | ID: mdl-38949063
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polystyrenes / Cell Culture Techniques / Dimethylpolysiloxanes Limits: Humans Language: En Journal: Lab Chip Journal subject: BIOTECNOLOGIA / QUIMICA Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polystyrenes / Cell Culture Techniques / Dimethylpolysiloxanes Limits: Humans Language: En Journal: Lab Chip Journal subject: BIOTECNOLOGIA / QUIMICA Year: 2024 Document type: Article