To develop an orthopedic scaffold that could overcome the limitations of implants used in clinics, we designed poly(ester-urethane) foams and compared their properties with those of a commercial gold standard. A degradable poly(ester-urethane) was synthetized by polyaddition between a diisocyanate poly(ε-caprolactone) prepolymer (PCL di-NCO, = 2400 g·mol) and poly(lactic--glycolic acid) diol (PLGA, = 2200 g·mol) acting as a chain extender. The resulting high-molecular-weight poly(ester-urethane) (PEU, = 87,000 g·mol) was obtained and thoroughly characterized by NMR, FTIR and SEC-MALS.
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