Integrated cascade nanozyme catalyzes in vivo ROS scavenging for anti-inflammatory therapy
Author(s) -
Yufeng Liu,
Yuan Cheng,
He Zhang,
Min Zhou,
Yijun Yu,
Shichao Lin,
Bo Jiang,
Xiaozhi Zhao,
Leiying Miao,
ChuanWan Wei,
Quanyi Liu,
YingWu Lin,
Yan Du,
Christopher J. Butch,
Hui Wei
Publication year - 2020
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.abb2695
Subject(s) - in vivo , scavenging , inflammation , reactive oxygen species , chemistry , cascade , computational biology , pharmacology , medicine , biology , biochemistry , immunology , microbiology and biotechnology , antioxidant , chromatography
Here, an integrated cascade nanozyme with a formulation of Pt@PCN222-Mn is developed to eliminate excessive reactive oxygen species (ROS). This nanozyme mimics superoxide dismutase by incorporation of a Mn-[5,10,15,20-tetrakis(4-carboxyphenyl)porphyrinato]-based metal-organic framework compound capable of transforming oxygen radicals to hydrogen peroxide. The second mimicked functionality is that of catalase by incorporation of Pt nanoparticles, which catalyze hydrogen peroxide disproportionation to water and oxygen. Both in vitro and in vivo experimental measurements reveal the synergistic ROS-scavenging capacity of such an integrated cascade nanozyme. Two forms of inflammatory bowel disease (IBD; i.e., ulcerative colitis and Crohn's disease) can be effectively relieved by treatment with the cascade nanozyme. This study not only provides a new method for constructing enzyme-like cascade systems but also illustrates their efficient therapeutic promise in the treatment of in vivo IBDs.
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