葡萄糖氧化酶
材料科学
级联
纳米技术
纳米-
催化作用
化学
生物传感器
生物化学
色谱法
复合材料
作者
Lie Wu,Yu Zhang,Li Chu,Chaolei Hua,Chenchen Chu,Mingyang Jiang,Qiongdi Zhang,Dandan Ma,Yijie Chen,Guan Liu,Chenying He,Xin Wang,Licheng Bai,Rui He,Xue‐Feng Yu,Wenhua Zhou,Shengyong Geng
标识
DOI:10.1002/adfm.202504434
摘要
Abstract The stability and activity of self‐cascade enzymes based on glucose oxidase (GOx) and peroxidase (POD) are usually low, which has significant limitations in tumor catalytic therapy. Building nanoislands‐supported single‐atom nanozymes with strong atomic‐nano interaction is an effective strategy for enhancing the self‐cascade enzyme‐like activity. Herein, noble metal iridium (Ir) single‐atoms are successfully deposited on CeO 2 quantum dots (QDs) nanoislands to construct Ir/CeO 2 single‐atom nanoislands (SANIs). The CeO 2 QDs nanoislands with abundant oxygen vacancies facilitate efficient electron transfer of Ir single‐atoms at the metal‐nanoislands interface. A liposomal nano platform encapsulated with Ir/CeO 2 SANIs (Ir/CeO 2 @Lipo) is further developed for in vivo catalytic therapy. The Ir/CeO 2 @Lipo exhibits excellent self‐cascade GOx‐ and POD‐like activity due to its unique atomic‐nano structures and the confined effect of the nanoislands. Compared with CeO 2 @Lipo and other reported nanozymes, Ir/CeO 2 @Lipo catalyzes glucose to generate more ROS with higher efficiency, demonstrating superior GOx‐POD self‐cascade enzyme‐like activity. In vivo, experiments demonstrate that Ir/CeO 2 @Lipo possesses excellent tumor‐targeting capability as well as nearly complete tumor ablation through ROS‐mediated apoptotic pathways. Thus, this work provides a new paradigm for designing self‐cascade enzymes for tumor treatment strategies.
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