催化作用
材料科学
星团(航天器)
Atom(片上系统)
金属
纳米技术
化学工程
冶金
化学
有机化学
计算机科学
工程类
嵌入式系统
程序设计语言
作者
Subin Yu,Haeun Kang,Seohyeon Jee,WooYeon Moon,Dohyub Jang,Wen‐Tse Huang,Dong-Jun Kim,Kyungwha Chung,Dong‐Il Won,Jungwon Park,Ru‐Shi Liu,Kyungmin Choi,Sehoon Kim,Luke P. Lee,Dong Ha Kim
标识
DOI:10.1002/adhm.202501058
摘要
Metal-organic frameworks (MOFs) are widely used as substrates for creating single-atom catalysts due to their abundance of ligands, facilitating enzyme-like activity for biomedical applications. However, the high-temperature calcination process for single-atom catalysts limits economical, efficient, and large-scale synthesis. Here, a simple room-temperature synthesis of MOF-based single-atom and metal cluster catalysts is presented for tumor therapy. Fe/MOF is obtained through a coordination reaction at room temperature, while Au/MOF is synthesized from Au3+/MOF by introducing a reducing agent. Au/MOF effectively generates hydrogen peroxide (H2O2) from glucose, outperforming Au3+/MOF, and Fe/MOF subsequently produced hydroxyl radicals (•OH) by decomposing the generated H2O2via accelerated peroxidase-like activity in an acidic environment. In vitro and in vivo studies confirm a significantly enhanced cancer eradication ability compared to the PBS-treated group by combining cascade enzymatic activity, destruction of oxidative homeostasis, and excessive mitochondrial-mediated lipid peroxidation. The novel synthesis process of MOF-based metal single-atom catalysts establishes a new paradigm for fabricating effective enzyme-like nanomaterials for multimodal tumor therapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI