| Literature DB >> 34668309 |
Jiang Ming1, Tianbao Zhu1, Jingchao Li2, Zichen Ye1, Changrong Shi2, Zhide Guo2, Jingjuan Wang1, Xiaolan Chen1, Nanfeng Zheng1.
Abstract
Nanozyme-based cascade reaction has emerged as an effective strategy for disease treatment because of its high efficiency and low side effects. Herein, a new and highly active two-dimensional Pd-Ru nanozyme is prepared and then integrated with uricase and red blood cell (RBC) membrane to fabricate a tandem nanoreactor, Pd-Ru/Uricase@RBC, for hyperuricemia treatment. The designed Pd-Ru/Uricase@RBC nanoreactor displayed not only good stability against extreme pH, temperature and proteolytic degradation, but also long circulation half-life and excellent safety. The nanoreactor can effectively degrade UA by uricase to allantoin and H2 O2 and remove H2 O2 by using Pd-Ru nanosheets (NSs) with the catalase (CAT)-like activity. More importantly, the finally produced O2 from H2 O2 decomposition can in turn facilitate the catalytic oxidation of UA, as the degradation of UA is an O2 consumption process. By integrating the high-efficiency enzymatic activity, long circulation capability, and good biocompatibility, the designed Pd-Ru/Uricase@RBC can effectively and safely treat hyperuricemia without side effects. The study affords a new alternative for the exploration of clinical treatment of hyperuricemia.Entities:
Keywords: cascade reaction; hyperuricemia treatment; nanozyme activity; red blood cell membrane coating; two-dimensional Pd-Ru nanosheets; uricase
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Year: 2021 PMID: 34668309 DOI: 10.1002/smll.202103645
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281