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

Jiaming Liu(Ministry of Education of the People's Republic of China), Jiaming Liu(Ministry of Education of the People's Republic of China), Aizhu Wang(University of Jinan), Shihui Liu(University of Jinan), Ruiqi Yang(Ministry of Education of the People's Republic of China), Longwei Wang(Ministry of Education of the People's Republic of China), Fene Gao(Ministry of Education of the People's Republic of China), Huige Zhou(University of Jinan), Xin Yu(Ministry of Education of the People's Republic of China), Jing Liu(Ministry of Education of the People's Republic of China), Jing Liu(Ministry of Education of the People's Republic of China), Chunying Chen(National Center for Nanoscience and Technology)
Angewandte Chemie International Edition
August 28, 2021
Cited by 174

Abstract

Abstract 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 H 2 O 2 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.


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