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Issue 6, 2007
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A practical guide to microfluidic perfusion culture of adherent mammalian cells

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Culturing cells at microscales allows control over microenvironmental cues, such as cell–cell and cell–matrix interactions; the potential to scale experiments; the use of small culture volumes; and the ability to integrate with microsystem technologies for on-chip experimentation. Microfluidic perfusion culture in particular allows controlled delivery and removal of soluble biochemical molecules in the extracellular microenvironment, and controlled application of mechanical forces exerted via fluid flow. There are many challenges to designing and operating a robust microfluidic perfusion culture system for routine culture of adherent mammalian cells. The current literature on microfluidic perfusion culture treats microfluidic design, device fabrication, cell culture, and micro-assays independently. Here we systematically present and discuss important design considerations in the context of the entire microfluidic perfusion culture system. These design considerations include the choice of materials, culture configurations, microfluidic network fabrication and micro-assays. We also present technical issues such as sterilization; seeding cells in both 2D and 3D configurations; and operating the system under optimized mass transport and shear stress conditions, free of air-bubbles. The integrative and systematic treatment of the microfluidic system design and fabrication, cell culture, and micro-assays provides novices with an effective starting point to build and operate a robust microfludic perfusion culture system for various applications.

Graphical abstract: A practical guide to microfluidic perfusion culture of adherent mammalian cells

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Publication details

The article was received on 28 Mar 2007, accepted on 16 Apr 2007 and first published on 11 May 2007

Article type: Tutorial Review
DOI: 10.1039/B704602B
Citation: Lab Chip, 2007,7, 681-694

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    A practical guide to microfluidic perfusion culture of adherent mammalian cells

    L. Kim, Y. Toh, J. Voldman and H. Yu, Lab Chip, 2007, 7, 681
    DOI: 10.1039/B704602B

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