尿酸
过氧化氢酶
活性氧
痛风
炎症
化学
非布索坦
医学
生物化学
内科学
酶
作者
Anqi Lin,Ziying Sun,Xingquan Xu,Sheng Zhao,Jiawei Li,Heng Sun,Quan Wang,Qing Jiang,Hui Wei,Dongquan Shi
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-12-30
卷期号:22 (1): 508-516
被引量:17
标识
DOI:10.1021/acs.nanolett.1c04454
摘要
Uricase-based therapies are limited for gout partially due to the accumulation of H2O2 in an arthrosis environment with slow metabolism. To tackle this limitation, previous studies adopted a cascade reaction between the degradation of uric acid (UA) and timely elimination of H2O2 using complicated composites of uricase and catalase (CAT)/CAT-like nanozyme. Herein, the self-cascade nanozyme Pt/CeO2 with high efficiency toward simultaneous UA degradation and H2O2 elimination is demonstrated on the basis of both uricase- and CAT-like activities in Pt, Ir, Rh, and Pd platinum-group metals. With an optimized molar ratio of Pt and CeO2, Pt/CeO2 (1/5) not only does better in degrading UA but also has excellent reactive oxygen species (ROS) and reactive nitrogen species (RNS) scavenging activities. In monosodium urate (MSU)-induced acute gout rats, Pt/CeO2 nanozyme markedly alleviates pain along with joint edema, thus improving gait claudication and tissue inflammation. These results provide novel insights into strategies of an efficient enzyme-mimetic treatment for gout.
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