Construction of Au@MnO 2 Yolk-in-Shell Nanostructures as Uricase Mimics for Efficient Hyperuricemia Therapy

高尿酸血症 尿酸 纳米结构 催化作用 化学 纳米技术 活性氧 纳米颗粒 催化效率 氧气 尿酸氧化酶 材料科学 生物化学 吸附
作者
Jun Hu,Rufang Zhao,Zhilong Xu,Zheng Xi,Jie Gu,Xiaohuan Sun,Juqun Xi,Yan Liu,Jie Han
出处
期刊:Langmuir [American Chemical Society]
卷期号:41 (44): 29826-29837
标识
DOI:10.1021/acs.langmuir.5c04317
摘要

Hyperuricemia, marked by elevated blood uric acid levels, poses significant health risks. Current uricase-based treatments have a serious issue of H 2 O 2 and reactive oxygen species (ROS) accumulation. MnO 2 -based nanozymes have been demonstrated to possess uricase-like catalytic activity, but with the limitations of low catalytic performance and poor H 2 O 2 and ROS removal ability. This study investigates a novel nanostructure of the Au@MnO 2 yolk-in-shell for managing hyperuricemia. This unique nanohybrid structure, with an individual Au nanoparticle embedded within the hollow MnO 2 shell, reduces the Au loading and shows exceptional uricase-like catalytic performance. Density functional theory calculations reveal the existence of the strong synergistic interactions between the Au and MnO 2 interface layer within this structure, and the introduction of Au increases adsorption energies for both oxygen and uric acid on MnO 2, facilitating an efficient catalytic process. The Au@MnO 2 yolk-in-shell nanostructure exhibits excellent metabolic rates, good biocompatibility, and superior therapeutic effects. (The blood uric acid level is decreased by 71%, and both liver and kidney functions return to normal). These findings underscore the Au@MnO 2 yolk-in-shell nanostructure as a promising candidate for hyperuricemia treatment. This approach paves the way for efficient, cost-effective therapies and provides valuable insights into enhancing enzyme activity in various applications.
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