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A Facile and Eco-friendly Route to Fabricate Poly(Lactic Acid) Scaffolds with Graded Pore Size
Published on: October 17, 2016
Embroidered and surface modified polycaprolactone-co-lactide scaffolds as bone substitute: in vitro characterization
Barbe Rentsch1, Andre Hofmann, Annette Breier
1Catgut GmbH, Markneukirchen, Germany. catgut.office@catgut.de
Annals of Biomedical Engineering
|July 24, 2009
Summary
This study developed a modified polycaprolactone scaffold for bone tissue engineering. The enhanced scaffold promotes human mesenchymal stem cell adhesion, proliferation, and osteogenic differentiation, showing potential as a bioartificial bone substitute.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Regenerative Medicine
Background:
- Bone tissue engineering requires scaffolds that support cell activity and bone formation.
- Polycaprolactone (PCL) is a biodegradable polymer with potential for bone regeneration.
- Surface modification and biomolecule coating can improve scaffold performance.
Purpose of the Study:
- To evaluate an embroidered PCL scaffold modified with NaOH, collagen I (coll I), and chondroitin sulfate (CS) for bone tissue engineering.
- To investigate the effects of surface modifications and biomolecule coatings on human mesenchymal stem cell (hMSC) behavior.
- To assess the scaffold's potential as a bioartificial bone substitute.
Main Methods:
- Fabrication of embroidered PCL scaffolds with controlled porosity (80%) and pore size (0.2-1 mm).
- Surface hydrolysis of PCL scaffolds using NaOH to enhance hydrophilicity.
- Coating of scaffolds with collagen I and chondroitin sulfate.
- Evaluation of cell adhesion, proliferation, and osteogenic differentiation of hMSCs on the modified scaffolds.
Main Results:
- NaOH treatment increased surface hydrophilicity (water contact angle to 25%) and enhanced collagen I adsorption (up to 15%) and cell attachment (2x).
- Collagen I coating significantly improved hMSC attachment and proliferation (3x).
- Chondroitin sulfate induced osteogenic differentiation of hMSCs without additional additives.
- The modified scaffolds demonstrated suitability for cell migration, proliferation, and differentiation.
Conclusions:
- The modified PCL scaffold effectively supports hMSC adhesion, proliferation, and osteogenic differentiation.
- Surface functionalization with collagen I and chondroitin sulfate is crucial for enhancing biological responses.
- These scaffolds show significant promise as bioartificial bone substitutes for bone regeneration applications.

