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Cell-laden microfibers fabricated using μl cell-suspension
Minghao Nie1, Shogo Nagata2, Hoshimi Aoyagi2
1Department of Information Science and Technology, The University of Tokyo, Tokyo, Japan.
Biofabrication
|April 17, 2020
Summary
This study introduces a novel microfluidic method for creating cell-laden microfibers using minimal cell suspension volumes. This technique reduces costs and time, making rare cell research more accessible.
Area of Science:
- Biotechnology
- Microfluidics
- Tissue Engineering
Background:
- Conventional microfluidic methods for cell-laden microfiber fabrication demand large cell suspension volumes (>100 μl).
- Acquiring sufficient rare cells for high-density suspensions is costly and time-consuming.
- A need exists for microfluidic techniques that efficiently utilize small cell volumes.
Purpose of the Study:
- To develop a facile microfluidic method for fabricating cell-laden microfibers from small-volume cell suspensions.
- To enable the use of rare or limited cell samples in microfiber fabrication.
- To reduce material and time consumption in cell-laden microfiber production.
Main Methods:
- Utilized a 3D-printed coaxial microfluidic device.
- Incorporated a 'luer-lock inlet' for deterministic loading of small cell suspension volumes (as low as 5 μl).
- Demonstrated fabrication of fibrous tissues with various cell types.
Main Results:
- Successfully fabricated cell-laden microfibers using only 5 μl of cell suspension with minimal sample loss.
- Formed fibrous tissues composed of diverse cell types.
- Confirmed that the fabrication process does not significantly affect encapsulated cell morphology or function.
- Showcased potential for quantitative assays on fiber-shaped tissues.
Conclusions:
- The developed microfluidic method efficiently produces cell-laden microfibers from small cell volumes.
- This approach significantly reduces the cost and time associated with rare cell research.
- The method preserves cell viability and function, enabling downstream applications like quantitative assays.

