| Literature DB >> 35233936 |
Xiangfu Meng1,2, Ke Zhou3,4, Yong Qian1,2, Hongji Liu1,2, Xingyu Wang1,2, Yefeng Lin1,2, Xinyi Shi1,2, Yu Tian3, Yijun Lu2,3, Qianwang Chen2, Junchao Qian3,5, Hui Wang1,2.
Abstract
Cuprous-based nanozymes have demonstrated great potential for cascade chemodynamic therapy (CDT) due to their higher catalytic efficiency and simple reaction conditions. Here, hollow cuprous oxide@nitrogen-doped carbon (HCONC) dual-shell structures are designed as nanozymes for CDT oncotherapy. This HCONC with a size distribution of 130 nm is synthesized by a one-step hydrothermal method using cupric nitrate and dimethyl formamide as precursors. The thin-layer carbon (1.88 nm) of HCONC enhances the water-stability and reduces the systemic toxicity of cuprous oxide nanocrystals. The dissolved Cu+ of HCONC in acid solution induces a Fenton-like reaction and exhibits a fast reaction rate for catalyzing H2 O2 into highly toxic hydroxyl radicals (·OH). Meanwhile, the formed Cu+ consumes oversaturated glutathione (GSH) to avoid its destruction of ROS at the intracellular level. In general, both cellular and animal experiments show that HCONC demonstrates excellent antitumor ability without causing significant systemic toxicity, which may present tremendous potential for clinical cancer therapy.Entities:
Keywords: cascade reactions; chemodynamic therapy; cuprous oxides; dual-shell structures; hollow cavity
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Year: 2022 PMID: 35233936 DOI: 10.1002/smll.202107422
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281