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Fabrication of Decellularized Cartilage-derived Matrix Scaffolds
Published on: January 7, 2019
A biocompatible tissue scaffold produced by supercritical fluid processing for cartilage tissue engineering.
Su Hee Kim1, Youngmee Jung, Soo Hyun Kim
1Center for Biomaterials, Korea Institute of Science and Technology, Seoul, Korea.
Tissue Engineering. Part C, Methods
|July 28, 2012
Summary
Supercritical fluid processing offers a non-toxic, efficient method for creating elastic Poly(L-lactide-co-ɛ-caprolactone) scaffolds for cartilage tissue engineering. This technique yields superior porous structures and enhanced in vivo tissue regeneration compared to traditional solvent-based methods.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Polymer Chemistry
Background:
- Supercritical fluids, particularly supercritical carbon dioxide (ScCO(2)), offer advantageous properties like non-flammability and low cost.
- Poly(L-lactide-co-ɛ-caprolactone) (PLCL) is a promising elastic polymer for cartilage tissue engineering.
- Conventional PLCL scaffold fabrication using organic solvents poses risks of cytotoxicity and lengthy processing times.
Purpose of the Study:
- To fabricate mechano-active PLCL scaffolds using supercritical fluid processing for cartilage tissue engineering.
- To compare the physical and biological performance of ScCO(2)-processed PLCL scaffolds against those made by solvent-casting.
- To investigate the optimal conditions (pressure, temperature, depressurization rate) for PLCL foaming using ScCO(2).
Main Methods:
- Fabrication of PLCL scaffolds using supercritical fluid processing with ScCO(2).
- Characterization of scaffold porosity, pore size distribution, and interconnectedness.
- Assessment of scaffold cytotoxicity using in vitro cell seeding.
- In vivo evaluation of cell-scaffold constructs implanted in nude mice for 4 weeks.
Main Results:
- Scaffolds produced by supercritical fluid processing exhibited a homogeneous, interconnected porous structure with narrow pore size distribution.
- No cytotoxicity was observed in ScCO(2)-processed PLCL scaffolds, unlike solvent-pressed scaffolds.
- In vivo studies showed superior cartilaginous tissue formation and extracellular matrix accumulation in ScCO(2)-processed scaffolds.
Conclusions:
- Supercritical fluid processing provides a non-toxic, efficient alternative for fabricating PLCL scaffolds for cartilage tissue engineering.
- The resulting scaffolds possess well-interconnected, non-toxic porous structures ideal for cell growth.
- Elastic PLCL scaffolds fabricated via ScCO(2) demonstrate significant potential for advanced cartilage tissue regeneration applications.

