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Image-guided, Laser-based Fabrication of Vascular-derived Microfluidic Networks
Published on: January 3, 2017
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Vascular-like network prepared using hollow hydrogel microfibers
Takayuki Takei1, Zyunpei Kitazono1, Yoshihiro Ozuno1
1Department of Chemical Engineering, Graduate School of Science and Engineering, Kagoshima University, 1-21-40 Korimoto, Kagoshima 890-0065, Japan.
Journal of Bioscience and Bioengineering
|July 23, 2015
Summary
Researchers developed a novel vascular-like network using alginate hydrogel microfibers. This technique enables rapid nutrient perfusion and cell viability, crucial for creating volumetric tissues in vitro.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Regenerative Medicine
Background:
- Creating volumetric tissues in vitro requires a 3D vascular-like network for cell survival.
- Efficient oxygen and nutrient supply necessitates microvessel channels within 100-200 μm.
- Rapid perfusion of medium or blood post-cell seeding is critical.
Purpose of the Study:
- To develop a novel technique for fabricating engineered vascular-like networks.
- To meet the critical requirements of channel distance and rapid perfusion for tissue engineering.
Main Methods:
- Fabrication of assembled hollow alginate hydrogel microfibers.
- Enclosing mammalian cells within the gel portions of the microfibers.
- Controlling microfiber gel thickness to achieve desired channel spacing (approx. 50 μm gel, <150 μm channel distance).
Main Results:
- Achieved microchannel distances within 150 μm using 50 μm gel thickness microfibers.
- Confirmed rapid medium perfusion (<10 min) after cell immobilization.
- Demonstrated HepG2 cell proliferation and function maintenance in gel portions during 7-day perfusion culture.
Conclusions:
- The novel vascular-like networks satisfy key requirements for volumetric tissue engineering.
- This technique shows potential for advancing in vitro tissue and organ creation.
- Successful cell function and viability highlight the network's suitability for perfusion culture.

