Abstract
Catalysis is a fundamental principle of biological systems, yet synthetic biomaterials seldom incorporate catalytic activity as a core design principle. Here, we introduce a polymeric network constructed by crosslinking imidazole-functionalized polymers using Cu2+ ions, yielding an elastomer with enzyme-mimetic reactivity. This bioinspired design enables sustained nitric oxide (NO) generation in serum and broad-spectrum antioxidant activity against superoxide, hydrogen peroxide, and hydroxyl radicals, mimicking the functions of superoxide dismutase, catalase, and peroxidases. Catalytic activity depends on Cu2+ coordination, confirming a defined structure-function mechanism. The elastomer demonstrates minimal hemolysis, reduced platelet adhesion, and high biocompatibility upon subcutaneous implantation. Remarkably, the material can be fully recycled by a simple immersion in acetic acid that reverses Cu2+ coordination without compromising the integrity of the polymer. This closed-loop feature aligns with circular economy principles and greatly extends the functional lifespan of the material. By integrating mechanical robustness, catalytic activity, and recyclability, this material bridges a critical gap between natural and engineered systems, establishing a new framework for catalytically active and sustainable biomaterials.
| Original language | English |
|---|---|
| Pages (from-to) | 447-462 |
| Number of pages | 16 |
| Journal | Bioactive Materials |
| Volume | 62 |
| DOIs | |
| Publication status | Published - 1 Aug 2026 |
| Externally published | Yes |
Keywords
- NITRIC-OXIDE RELEASE
- HYDROGEN-PEROXIDE
- SUPEROXIDE-DISMUTASE
- COPPER
- POLYURETHANE
- GENERATION
- COMPLEXES
- STIFFNESS
- RADICALS
- ELASTIN
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