4.7 Article

Aspiration-mediated hydrogel micropatterning using rail-based open microfluidic devices for high-throughput 3D cell culture

Journal

SCIENTIFIC REPORTS
Volume 11, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41598-021-99387-6

Keywords

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Funding

  1. Ministry of Trade, Industry and Energy (MOTIE)
  2. Korea Institute for Advancement of Technology (KIAT) through the International Cooperative RD program [P0011266]
  3. National Research Foundation of Korea (NRF) - Korea government (MSIT) [NRF-2018052541, 2021R1A3B1077481]
  4. Ministry of Health & Welfare (MOHW), Republic of Korea [P0011266] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  5. National Research Foundation of Korea [2021R1A3B1077481] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Microfluidics offer promising methods for aligning cells in physiologically relevant configurations in order to recapitulate human organ functionality. A swift and robust hydrogel patterning technique is presented for 3D cell culture, demonstrating the potential for high-throughput cellular co-culture using a microfluidic device. This technique allows for the controlled formation of multiple, discontinuous hollow channels within the device.
Microfluidics offers promising methods for aligning cells in physiologically relevant configurations to recapitulate human organ functionality. Specifically, microstructures within microfluidic devices facilitate 3D cell culture by guiding hydrogel precursors containing cells. Conventional approaches utilize capillary forces of hydrogel precursors to guide fluid flow into desired areas of high wettability. These methods, however, require complicated fabrication processes and subtle loading protocols, thus limiting device throughput and experimental yield. Here, we present a swift and robust hydrogel patterning technique for 3D cell culture, where preloaded hydrogel solution in a microfluidic device is aspirated while only leaving a portion of the solution in desired channels. The device is designed such that differing critical capillary pressure conditions are established over the interfaces of the loaded hydrogel solution, which leads to controlled removal of the solution during aspiration. A proposed theoretical model of capillary pressure conditions provides physical insights to inform generalized design rules for device structures. We demonstrate formation of multiple, discontinuous hollow channels with a single aspiration. Then we test vasculogenic capacity of various cell types using a microfluidic device obtained by our technique to illustrate its capabilities as a viable micro-manufacturing scheme for high-throughput cellular co-culture.

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