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Published on: February 23, 2024
Three-dimensional porous polycaprolactone/chitosan/bioactive glass scaffold for bone tissue engineering
Kiran Joy1, Sathya Seeli David1, Abinaya Shanmugavadivu2
1Department of Chemistry, Hindustan Institute of Technology and Science, Padur, Chennai, India.
New polycaprolactone (PCL)/chitosan (CS)/bioactive glass (BG) scaffolds show promise for bone tissue engineering. These 3D porous materials exhibit excellent mechanical properties, biocompatibility, and osteogenic activity.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Nanotechnology
Background:
- Bone tissue engineering requires advanced biomaterials for regenerating bone defects.
- Polycaprolactone (PCL), chitosan (CS), and bioactive glass (BG) nanoparticles offer potential synergistic properties for scaffold development.
Purpose of the Study:
- To fabricate and characterize three-dimensional (3D) porous scaffolds from PCL/CS/BG nanoparticle composites.
- To evaluate the physiochemical, mechanical, degradation, bioactivity, and biocompatibility properties of the developed scaffolds for bone regeneration.
Main Methods:
- Freeze-drying technique for scaffold fabrication.
- Physicochemical characterization using FTIR, XRD, EDX, and SEM.
- Evaluation of swelling, porosity, water retention, compression strength, in vitro biodegradation, bioactivity, and biocompatibility.
Main Results:
- Scaffolds with 4 wt.% BG content exhibited optimal pore size (106 μm), porosity (156%), swelling (128%), water retention (179%), and compressive strength (3.7 MPa).
- The PCL/CS/BG scaffolds demonstrated controlled degradation, good antimicrobial activity, and excellent biocompatibility with C3H10T1/2 cells.
- Alizarin red staining confirmed the osteogenic activity of the composite scaffolds.
Conclusions:
- The fabricated PCL/CS/BG composite scaffolds possess suitable properties for bone tissue engineering applications.
- These scaffolds show potential for promoting bone regeneration due to their mechanical integrity, bioactivity, and biocompatibility.
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