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A Versatile Method of Patterning Proteins and Cells
Published on: February 26, 2017
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Patterning Biological Gels for 3D Cell Culture inside Microfluidic Devices by Local Surface Modification through
Joshua Loessberg-Zahl1, Jelle Beumer1, Albert van den Berg1
1BIOS/Lab on a Chip, University of Twente, 7500-AE Enschede, The Netherlands.
Micromachines
|December 19, 2020
Summary
This study introduces a new method for patterning hydrogels in microfluidic devices using laminar flow, avoiding complex fabrication. This technique enhances cell culture models and organs-on-chips by creating physiologically relevant microenvironments.
Area of Science:
- Biomedical Engineering
- Microfluidics
- Biomaterials Science
Background:
- Microfluidic devices are crucial for in vitro cell culture, particularly organs-on-chips.
- Patterning biological hydrogels provides controlled 3D microenvironments for cells.
- Existing hydrogel patterning methods often require costly fabrication and use non-physiological structures.
Purpose of the Study:
- To develop a facile hydrogel patterning technique for microfluidic devices.
- To overcome limitations of existing methods, such as cleanroom fabrication and non-physiological structures.
- To improve the design flexibility and physiological relevance of microfluidic cell culture models.
Main Methods:
- Utilized laminar flow patterning to create hydrophilic paths within hydrophobic microfluidic channels.
- Confined liquid hydrogels to these hydrophilic paths for precise geometry formation.
- Demonstrated patterning in various channel geometries with control over gel parameters.
Main Results:
- Successfully patterned hydrogel geometries without built-in channel confinement.
- Cultured human umbilical vein endothelial cells within patterned hydrogels for multiple days.
- Showcased cell migration into hydrogels under trans-gel flow and confirmed gel stability under physiological flow conditions.
Conclusions:
- The novel technique offers facile and versatile hydrogel patterning in microfluidics.
- It eliminates the need for complex fabrication and non-physiological structures.
- This method enhances the physiological realism and design efficiency of organs-on-chips and cell culture assays.

