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Dynamic cell seeding of polymer scaffolds for cartilage tissue engineering
G Vunjak-Novakovic1, B Obradovic, I Martin
1Division of Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA. gordana@mit.edu
Biotechnology Progress
|June 13, 1998
Summary
Optimizing cell seeding in large polymer scaffolds for tissue engineering requires high cell yield, rapid attachment, and uniform distribution. Mixing spinner flasks promotes cell aggregate formation, enhancing cartilage tissue regeneration efficiency.
Area of Science:
- Biomaterials Engineering
- Tissue Engineering
- Cell Biology
Background:
- Cell seeding is critical for engineered tissue development in bioreactors.
- Large scaffolds for clinical implants necessitate efficient cell seeding: high yield, fast kinetics, and uniform distribution.
- Anchorage-dependent and shear-sensitive cells require minimized suspension time.
Purpose of the Study:
- To investigate cell seeding kinetics and distribution in large polyglycolic acid scaffolds.
- To optimize cell seeding for cartilage tissue engineering using spinner flasks.
- To develop a mathematical model for predicting cell seeding efficiency.
Main Methods:
- Utilized highly porous, fibrous polyglycolic acid scaffolds (5-10 mm diameter, 2-5 mm thick).
- Employed bovine articular chondrocytes for cell seeding in well-mixed spinner flasks.
- Analyzed cell attachment kinetics and distribution throughout the scaffold volume.
Main Results:
- Achieved high cell attachment throughout the scaffold volume within 1 day.
- Mixing promoted the formation of 20-32 micron cell aggregates, enhancing attachment kinetics.
- Cell aggregate formation improved kinetics without compromising distribution uniformity.
Conclusions:
- Spinner flask mixing effectively seeds large scaffolds with chondrocytes.
- Cell aggregate formation is key to optimizing cell seeding for cartilage tissue engineering.
- A mathematical model can guide the optimization of cell seeding conditions.