A Titanium Nitride Nanozyme for pH-Responsive and Irradiation-Enhanced Cascade-Catalytic Tumor Therapy

被引:128
作者
Liu, Jiaming [1 ,2 ]
Wang, Aizhu [4 ]
Liu, Shihui [1 ,2 ]
Yang, Ruiqi [4 ]
Wang, Longwei [3 ]
Gao, Fene [1 ,2 ,3 ]
Zhou, Huige [1 ,2 ]
Yu, Xin [4 ]
Liu, Jing [1 ,2 ,3 ]
Chen, Chunying [1 ,2 ]
机构
[1] Univ Chinese Acad Sci, CAS Key Lab Biomed Effects Nanomat & Nanosafety, Natl Ctr Nanosci & Technol China, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, CAS Ctr Excellence Nanosci, Natl Ctr Nanosci & Technol China, Beijing 100190, Peoples R China
[3] Northwest Univ, Key Lab Resource Biol & Biotechnol Western China, Minist Educ, Sch Med, Xian 710069, Peoples R China
[4] Univ Jinan, Inst Adv Interdisciplinary Res, Jinan 250022, Peoples R China
基金
中国国家自然科学基金;
关键词
cascade catalysis; photothermal therapy; nanozyme; nitrogen-doping; titanium nitride; MICROENVIRONMENTAL REGULATION; HORSERADISH-PEROXIDASE; OXIDE NANOPARTICLES;
D O I
10.1002/anie.202106750
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanozyme-based catalytic tumor therapy is an emerging therapeutic method with high reactivity in response to tumor microenvironments (TMEs). To overcome the current limitations of deficient catalytic activity of nanozymes, we studied the contributing factors of enzymatic activity based on non-metallic-atom doping and irradiation. Nitrogen doping significantly enhanced the peroxidase activity of Ti-based nanozymes, which was shown experimentally and theoretically. Based on the excellent NIR-adsorption-induced surface plasmon resonance and photothermal effect, the enzymatic activity of TiN nanoparticles (NPs) was further improved under NIR laser irradiation. Hence, an acidic TME-responsive and irradiation-mediated cascade nanocatalyst (TLGp) is presented by using TiN-NP-encapsulated liposomes linked with pH-responsive PEG-modified glucose oxidase (GOx). The integration of pH-responsive GOx-mediated H2O2 self-supply, nitrogen-doping, and irradiation-enhanced enzymatic activity of TiN NPs and mild-photothermal therapy enables an effective tumor inhibition by TLGp with minimal side effects in vivo.
引用
收藏
页码:25328 / 25338
页数:11
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