Department of Cardiology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei 230036, China.
State Key Laboratory for Hubei New Textile Materials and Advanced Processing Technologies, School of Textile Science and Engineering, Wuhan Textile University, Wuhan 430200, China.
Biointerphases. 2022 May 2;17(3):031001. doi: 10.1116/6.0001690.
In situ release of nitric oxide (NO) has been suggested to be a potential functionalization strategy for blood-contacting implants. In this study, the NO generation capability catalyzed by the copper ion-incorporated silk fibroin (SF) films in the presence of S-nitroso-N-acetyl-dl-penicillamine (SNAP) is demonstrated. Cu(II) is effectively bound to the surface of the SF film based on metal-protein coordination. The x-ray photoelectron spectroscopy results indicate that copper ions may exist on the surface of the SF film in the form of Cu(II)/Cu(I) coexistence. The degradation behavior showed that the bound copper ions on the surface of the SF films can maintain a slow release in phosphate-buffered saline (PBS) or collagenase IA solution for 7 days. There was no significant difference in the release of copper ions between PBS degradation and enzyme degradation. The loading of copper ions significantly improved the release of NO from SNAP through catalysis. Based on the biological effects of copper ions and the ability to catalyze the release of NO from S-nitrosothiols, copper ion loading provides an option for the construction of bioactive SF biomaterials.
已有研究表明,通过原位释放一氧化氮(NO)可以作为一种潜在的功能化策略,用于血液接触型植入物。本研究展示了载铜丝素(SF)膜在 S-亚硝基-N-乙酰-DL-青霉胺(SNAP)存在的条件下催化产生 NO 的能力。铜(II)离子通过金属-蛋白配位有效地结合到 SF 膜表面。X 射线光电子能谱结果表明,铜离子可能以 Cu(II)/Cu(I)共存的形式存在于 SF 膜的表面。降解行为表明,SF 膜表面结合的铜离子在磷酸盐缓冲盐水(PBS)或胶原酶 IA 溶液中可保持 7 天的缓慢释放。在 PBS 降解和酶降解过程中,铜离子的释放没有明显差异。铜离子的负载通过催化显著提高了 SNAP 中 NO 的释放。基于铜离子的生物学效应和对 S-亚硝基硫醇释放 NO 的催化能力,铜离子负载为构建具有生物活性的 SF 生物材料提供了一种选择。