Atomic‐Level High‐Entropy Nanozymes Enable Remarkable Endogenous Targeted Catalysis and Enhancing Tumor Photothermal Therapy

Y Yongjian Ai Z Zhengyu Wang (School of Clinical Medicine, Shandong Second Medical University) W Wenhao Shi (Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry) X Xiaomeng Jia M Mengyang Cui (Department of Chemistry and the Waterloo Institute for Nanotechnology) H Hong‐bin Sun (Department of Chemistry Northeastern University Shenyang 110819 P.R. China) F Fazheng Ren M Meng‐Qi He (MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology Department of Chemistry Laboratory of Flexible Electronics Technology Center for Synthetic and Systems Biology Tsinghua University‐Peking University Joint Centre for Life Sciences Tsinghua University Beijing 100084 P. R. China) Q Qionglin Liang (MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology Department of Chemistry Laboratory of Flexible Electronics Technology Center for Synthetic and Systems Biology Tsinghua University‐Peking University Joint Centre for Life Sciences Tsinghua University Beijing 100084 P. R. China)

Abstract

AbstractNanozymes hold great potential in protecting human health. However, constructing new and efficient nanozymes is a significant challenge. Developing atomic‐level nanozymes is a promising approach. Despite their potential, atomic‐level high‐entropy nanozymes have not been reported due to thermodynamic instability. Therefore, developing atomic‐level high‐entropy nanozymes are of great significance. What's more, further exploring their biomedical applications can open up new horizons for nanozymology. Here, the atomic‐level high‐entropy nanozyme system capable of remarkable endogenous targeted catalysis and enhancing tumor photothermal therapy is successfully constructed. The system is prepared by reduction‐diffusion and grafting methods. The RuRhPtIrMo sub‐nanometer high‐entropy nanozyme (snHEAzyme) with about 8–10 atoms thickness is first prepared. Then, they are grafted by targeting agent DSPE‐PEG2000‐cRGD and imaging agent Cy7 to obtain the snHEAzyme@DSPE‐PEG2000‐cRGD@Cy7 nanozyme system. The synthesized snHEAzyme@DSPE‐PEG2000‐cRGD@Cy7 system exhibits excellent peroxidase‐like activity and high absorbance in the near‐infrared (NIR) range. Under NIR irradiation, the nanozyme shows efficient photothermal conversion and reactive oxygen species generation effects. In vitro and in vivo experiments demonstrated that the snHEAzyme@DSPE‐PEG2000‐cRGD@Cy7 system can be effectively targeted to penetrate tumor cell membranes and treat tumors. This work offers a new perspective on snHEAzyme fabrication and its biomedical applications.

Article Details

Volume / Issue Vol. 37, Issue 33
Published August 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (9)

Y

Yongjian Ai

Z

Zhengyu Wang

School of Clinical Medicine, Shandong Second Medical University

W

Wenhao Shi

Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry

X

Xiaomeng Jia

M

Mengyang Cui

Department of Chemistry and the Waterloo Institute for Nanotechnology

H

Hong‐bin Sun

Department of Chemistry Northeastern University Shenyang 110819 P.R. China

F

Fazheng Ren

M

Meng‐Qi He

MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology Department of Chemistry Laboratory of Flexible Electronics Technology Center for Synthetic and Systems Biology Tsinghua University‐Peking University Joint Centre for Life Sciences Tsinghua University Beijing 100084 P. R. China

Q

Qionglin Liang

MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology Department of Chemistry Laboratory of Flexible Electronics Technology Center for Synthetic and Systems Biology Tsinghua University‐Peking University Joint Centre for Life Sciences Tsinghua University Beijing 100084 P. R. China