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Synthesis, characterization and cytocompatibility of polyurethaneurea elastomers with designed elastase sensitivity.
Jianjun Guan1, William R Wagner
1McGowan Institute for Regenerative Medicine, University of Pittsburgh, 100 Technology Dr., Pittsburgh, Pennsylvania 15219, USA.
Biomacromolecules
|September 13, 2005
Summary
We developed new polyurethaneureas (PUs) for soft tissue engineering. These PUs offer tunable degradation, excellent mechanical properties, and enhanced cell adhesion, making them promising for tissue regeneration.
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Tissue Engineering
Background:
- Designing synthetic scaffolds for soft tissue engineering requires materials with elasticity, cell compatibility, processability, and in vivo remodeling capacity.
- Existing materials often lack a combination of mechanical strength, controlled degradation, and bioactivity.
Purpose of the Study:
- To develop and characterize a novel family of polyurethaneureas (PUs) with enzymatic remodeling capabilities for soft tissue engineering applications.
- To evaluate the mechanical properties, hydrolytic and enzymatic degradation, and cell adhesion characteristics of these PUs.
Main Methods:
- Polyurethaneureas (PUs) were synthesized using polycaprolactone or PCL-PEG-PCL as soft segments, 1,4-butanediisocyanate as the hard segment, and Ala-Ala-Lys as a chain extender.
- Mechanical properties (tensile strength, breaking strain) and thermal properties (glass transition temperature) were assessed.
- In vitro degradation studies were performed in buffered saline with and without elastase.
- Surface modification with Arg-Gly-Asp-Ser (RGDS) was achieved via radio frequency glow discharge.
- Endothelial cell adhesion was quantified on pristine and modified PU surfaces.
Main Results:
- Synthesized PUs exhibited high molecular weights, low glass transition temperatures (< -54°C), high flexibility (670-890% strain), and significant tensile strength (15-28 MPa).
- PUs showed controlled hydrolytic degradation (12-18% mass loss over 8 weeks) and significantly enhanced degradation in the presence of elastase (19-34% mass loss).
- Degradation products were non-cytotoxic, and surface modification with RGDS increased endothelial cell adhesion by over 200% compared to tissue culture polystyrene.
Conclusions:
- The developed polyurethaneureas possess a unique combination of mechanical robustness, tunable enzymatic degradability, and enhanced cell interactivity.
- These PUs show significant potential as versatile scaffolds for soft tissue engineering, facilitating cell integration and tissue remodeling.
- The material's properties can be tailored by adjusting the soft segment composition for specific regenerative medicine applications.

