Biodegradable synthetic polymers have been widely used as tissue
engineering scaffold materials. Even though they have shown excellent
biocompatibility, they have failed to resemble the low stiffness and high
elasticity of soft tissues because of the presence of massive rigid ester bonds.
Herein, we synthesized a new thermoplastic polyurethane elastomer (CTC-PU(BET))
using poly ester ether triblock copolymer
(polycaprolactone-block-polytetrahydrofuran-block-polycaprolactone triblock
copolymer, PCTC) as the soft segment, aliphatic diisocyanate (hexamethylene
diisocyanate, HDI) as the hard segment, and degradable diol (bis(2-hydroxyethyl)
terephthalate, BET) as the chain extender. PCTC inhibited crystallization and
reduced the melting temperature of CTC-PU(BET), and BET dramatically enhanced
the thermal decomposition and hydrolytic degradation rate when compared with
conventional polyester-based biodegradable TPUs. The CTC-PU(BET) synthesized in
this study possessed a low tensile modulus and tensile strength of 2.2 MPa and
1.3 MPa, respectively, and an elongation-at-break over 700%. Meanwhile,
it maintained a 95.3% recovery rate and 90% resilience over ten
cycles of loading and unloading. In addition, the TPU could be electrospun into
both random and aligned fibrous scaffolds consisting of major microfibers and
nanobranches. 3T3 fibroblast cell culture confirmed that these scaffolds
outperformed the conventional biodegradable TPU scaffolds in terms of
substrate–cellular interactions and cell proliferation. Considering the
advantages of this TPU, such as ease of synthesis, low cost, low stiffness, high
elasticity, controllable degradation rate, ease of processability, and excellent
biocompatibility, it has great prospects to be used as a tissue engineering
scaffold material for soft tissue regeneration.