活性氧
化学
体内
催化作用
细胞内
过氧化氢酶
碳纤维
癌症研究
活性氮物种
超氧化物歧化酶
纳米技术
生物物理学
材料科学
肿瘤微环境
酶
生物化学
肿瘤细胞
生物
复合材料
生物技术
复合数
作者
Kelong Fan,Juqun Xi,Lei Fan,Peixia Wang,Chunhua Zhu,Yan Tang,Xiangdong Xu,Minmin Liang,Bing Jiang,Xiyun Yan,Lizeng Gao
标识
DOI:10.1038/s41467-018-03903-8
摘要
Nanomaterials with intrinsic enzyme-like activities (nanozymes), have been widely used as artificial enzymes in biomedicine. However, how to control their in vivo performance in a target cell is still challenging. Here we report a strategy to coordinate nanozymes to target tumor cells and selectively perform their activity to destruct tumors. We develop a nanozyme using nitrogen-doped porous carbon nanospheres which possess four enzyme-like activities (oxidase, peroxidase, catalase and superoxide dismutase) responsible for reactive oxygen species regulation. We then introduce ferritin to guide nitrogen-doped porous carbon nanospheres into lysosomes and boost reactive oxygen species generation in a tumor-specific manner, resulting in significant tumor regression in human tumor xenograft mice models. Together, our study provides evidence that nitrogen-doped porous carbon nanospheres are powerful nanozymes capable of regulating intracellular reactive oxygen species, and ferritinylation is a promising strategy to render nanozymes to target tumor cells for in vivo tumor catalytic therapy.
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