Abstract

Abstract 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.

Keywords

Reactive oxygen speciesChemistryIn vivoCatalaseIntracellularCatalysisTumor microenvironmentReactive nitrogen speciesSuperoxide dismutaseCarbon fibersBiophysicsNanotechnologyEnzymeBiochemistryTumor cellsMaterials scienceCancer researchBiology

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Publication Info

Year
2018
Type
article
Volume
9
Issue
1
Pages
1440-1440
Citations
1006
Access
Closed

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Kelong Fan, Juqun Xi, Lei Fan et al. (2018). In vivo guiding nitrogen-doped carbon nanozyme for tumor catalytic therapy. Nature Communications , 9 (1) , 1440-1440. https://doi.org/10.1038/s41467-018-03903-8

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DOI
10.1038/s41467-018-03903-8