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Biodegradable Water-Based Polyurethane Shape Memory Elastomers for Bone Tissue Engineering.

Yu-Jen Wang1, U-Ser Jeng2, Shan-Hui Hsu1,3,4

  • 1Institute of Polymer Science and Engineering, National Taiwan University, No. 1 Sec. 4 Roosevelt Road, Taipei 10617, Taiwan, R.O.C.

ACS Biomaterials Science & Engineering
|January 9, 2021
PubMed
Summary
This summary is machine-generated.

Biodegradable shape memory polyurethane scaffolds with superparamagnetic iron oxide nanoparticles promote bone regeneration. These 3D printed bone scaffolds offer improved osteogenic induction and may serve as customized bone substitutes.

Keywords:
3D printed scaffoldbone tissue engineeringmesenchymal stem cells (MSCs)shape memory polyurethane elastomersuperparamagnetic iron oxide

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Area of Science:

  • Biomaterials Science
  • Tissue Engineering
  • Polymer Chemistry

Background:

  • Shape memory polymers (SMPs) offer unique properties for biomedical applications.
  • Biodegradable SMPs are promising for bone scaffolds.
  • Superparamagnetic iron oxide nanoparticles (SPIO NPs) enhance osteogenic induction in human mesenchymal stem cells (hMSCs).

Purpose of the Study:

  • To synthesize and characterize water-based biodegradable shape memory polyurethane (PU) ink for 3D printing bone scaffolds.
  • To incorporate SPIO NPs into PU scaffolds to promote osteogenic induction and improve shape fixity.
  • To evaluate the printability, shape memory properties, and osteogenic potential of the fabricated scaffolds.

Main Methods:

  • Synthesized water-based biodegradable shape memory PU ink with SPIO NPs and viscosity enhancers (PEO or gelatin).
  • Fabricated bone scaffolds using a microextrusion-based low-temperature fuse deposition manufacturing (LFDM) platform.
  • Assessed scaffold printability, shape memory properties (fixity and recovery) in air and water, and hMSC proliferation and osteogenesis.

Main Results:

  • Both PU-PEO and PU-gelatin inks exhibited excellent printability.
  • PU-PEO scaffolds demonstrated superior shape fixity and recovery compared to PU-gelatin scaffolds.
  • Scaffolds with SPIO NPs significantly enhanced osteogenesis, with PU/PEO/SPIO showing faster SPIO release and greater osteogenic effect (2.7x increase in collagen) than PU/gelatin/SPIO (1.5x increase).
  • Gelatin-based scaffolds showed better hMSC proliferation, indicating higher biocompatibility than PEO-based scaffolds.

Conclusions:

  • 3D printed biodegradable PU scaffolds incorporating SPIO NPs possess shape memory properties and osteogenic potential.
  • These scaffolds are suitable for bone tissue engineering and could be utilized as customized bone substitutes in minimally invasive surgery.
  • The combination of biodegradability, shape memory effect, and osteoinductive properties makes these scaffolds highly promising for orthopedic applications.