Multi-enzymatic activities of ultrasmall ruthenium oxide for anti-inflammation and neuroprotection
[Display omitted] •Single-component RuO2 nanozymes featured five enzymatic activities.•RuO2-PVP NPs scavenged multi-ROS of H2O2, ·OH and O2·−.•Cellular lipid, DNA and protein were protected with RuO2-PVP antioxidant.•The antioxidant ameliorated inflammation and Parkinson's disease. Artificial e...
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Veröffentlicht in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2021-05, Vol.411, p.128543, Article 128543 |
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Format: | Artikel |
Sprache: | eng |
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•Single-component RuO2 nanozymes featured five enzymatic activities.•RuO2-PVP NPs scavenged multi-ROS of H2O2, ·OH and O2·−.•Cellular lipid, DNA and protein were protected with RuO2-PVP antioxidant.•The antioxidant ameliorated inflammation and Parkinson's disease.
Artificial enzymes to mimic the endogenous antioxidant system are promising candidates for treating and manipulating the in vivo dysregulated redox homeostasis. Though progresses have been made for reactive oxygen species (ROS) scavenging using nanozymes, nanomaterials with advanced multi-enzymatic activities and enhanced biocompatibility have been rarely explored. Herein, we report the facile construction of RuO2-PVP nanoparticles, as a single-component, multi-enzyme-mimicking nano-platform for multi-ROS scavenging, which simultaneously shows multi-enzymatic antioxidant activities mimicking intrinsic catalase, superoxide dismutase, peroxidase, as well as ascorbate peroxidase and thiol peroxidase. Owing to the multifunctional self-synergistic inhibitions on multi-ROS, e.g., H2O2, ·OH and O2·−, the fabricated RuO2-PVP nanozymes demonstrate a prominent redox homeostasis protection effect, which not only protects lipid, DNA and protein from damages by UV/H2O2/Fenton stimulation in vitro, but also performs magnificent ROS elimination properties against inflammation and Parkinson's disease in vivo. The constructed RuO2-based nanozymes provide a potential therapeutic nano-platform for the treatment of oxidative stress-related diseases. |
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ISSN: | 1385-8947 1873-3212 |
DOI: | 10.1016/j.cej.2021.128543 |