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Core/shell Printing Scaffolds For Tissue Engineering Of Tubular Structures
Published on: September 27, 2019
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Polyester-based ink platform with tunable bioactivity for 3D printing of tissue engineering scaffolds
Shen Ji1, Koustubh Dube, Julian P Chesterman
1Otto H. York Chemical and Materials Engineering, New Jersey Institute of Technology, 161 Warren Street, Newark, NJ 07102, USA. muratg@njit.edu.
Biomaterials Science
|December 12, 2018
Summary
Researchers developed a new 3D printable polymer for medical devices. This biodegradable material, functionalized with heparin and BMP-2, enhanced bone cell growth in 3D printed scaffolds.
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Additive Manufacturing
Background:
- Biodegradable polymers are crucial for medical implants and tissue engineering scaffolds.
- Developing materials with tunable properties and functionalizability for 3D printing remains a challenge.
- Existing materials often lack the necessary mechanical strength, printability, or bioactive integration for advanced applications.
Purpose of the Study:
- To synthesize a novel, tunable, and functionalizable polymeric biomaterial platform for extrusion-based 3D printing.
- To create biodegradable polymers with enhanced crystallinity and controlled degradation rates.
- To demonstrate the utility of this platform for creating bioactive scaffolds that promote osteogenic differentiation.
Main Methods:
- Synthesis of biodegradable polymers using 4-hydroxyphenethyl 2-(4-hydroxyphenyl)acetate (HTy) and p-phenylenediacetic acid (PDA), incorporating glutamic acid derivatives.
- Characterization of polymer properties including melting temperatures, Young's moduli, print temperatures, and hydrolytic degradation rates.
- Functionalization of polymers using click-based chemistry and fabrication of 3D printed scaffolds for cell culture studies.
Main Results:
- Novel copolymers (HP5GH, HP5GP, HP5BG) exhibited tunable properties suitable for 3D printing (170-190 °C) with Young's moduli of 1.9-2.4 GPa.
- HP5BG showed gradual degradation (∼30% Mw retained after 25 weeks), while HP5GP and HP5GH degraded faster (18% Mw retained after 8 weeks).
- 3D printed scaffolds from HP5GP functionalized with azide-Heparin and BMP-2 significantly enhanced osteogenic differentiation of human mesenchymal stem cells (hMSCs).
Conclusions:
- A novel, tunable, and functionalizable polymeric biomaterial platform for 3D printing has been successfully developed.
- The platform allows for controlled degradation and facile functionalization, enabling the creation of bioactive medical devices.
- This technology holds significant potential for additive manufacturing of scaffolds for bone regeneration and other medical applications.
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