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
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]
日期:2025-10-31
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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