PPDO/PCL/PEG Based Amphiphilic Polyurethanes with Controllable Degradation and Mechanical Retention

Abstract

Polyester-based biodegradable polymers are widely used in absorbable medical devices, however, the hydrophobic essence of polyesters limits the implanted applications in the conditions required rapid degradation. This work reported poly(p-dioxanone) (PPDO) based short-term degradable polyurethanes with controllable degradation and mechanical properties. Three polyurethanes composed of poly(ε-caprolactone) (PCL), poly(p-dioxanone)-poly(ethylene glycol)-poly(p-dioxanone) (PPDO-PEG-PPDO) triblock copolymer and polyethylene glycol (PEG) were synthesized with hexamethylene diisocyanate (HDI) as chain-extender. The resulted polyurethanes exhibited a desirable balance of tensile strength (>20 MPa) and exceptional extensibility (elongation at break >1100%) as well as tunable stiffness (Young’s modulus, 12 ~ 54 MPa). In artificial urine, the copolymers (PDEUs) exhibited composition-dependent mechanical degradation. The mechanical performance decreased in a near-linear time-dependent and the mechanical persistence times were 12, 34, and 52 days for PDEU1.5, PDEU3.5, and PDEU5.5, respectively. The structural analyses showed that the degradation was dominated by PPDO chain scission and depletion of a PPDO-rich amorphous phase, whereas PCL crystallinity provided structural stabilization. Additionally, PEG was largely retained to maintain hydrophilicity of the degradation products. Overall, the degradation kinetics and mechanical lifetime of PDEUs could be tailored by adjusting PPDO/PCL compositions for providing hydrophilic copolymers with rapid and controllable degradation in biomedical applications.

Supplementary files

Article information

Article type
Paper
Submitted
21 Feb 2026
Accepted
17 Apr 2026
First published
24 Apr 2026

New J. Chem., 2026, Accepted Manuscript

PPDO/PCL/PEG Based Amphiphilic Polyurethanes with Controllable Degradation and Mechanical Retention

Y. Chen, Q. Wang, Y. Bai, J. Li, N. Zhang and B. He, New J. Chem., 2026, Accepted Manuscript , DOI: 10.1039/D6NJ00659K

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