NIR-II/pH Dual Responsive CuHDB@CaP Nanospheres as a Self-Cascading Catalytic Platform for Highly Efficient Combating Bacterial Infections

The misuse of antibiotics has led to a dramatic increase in bacterial resistance, creating an urgent need for efficient antimicrobial agents with multiple mechanisms of action. In this study, Cu was modified with berberine derivatives, and a core–shell structure was successfully developed, resulting in a light/pH-responsive CuHDB@CaP nanotherapeutic platform. It achieves controlled release of CuHDB nanozymes, with CaP, which is highly stable in neutral or alkaline environments, preventing CuHDB leakage and effectively “switching off” the activity of nanozymes. Bacterial metabolism, which produces lactic and keto acids, lowers the pH of the wound microenvironment. Additionally, exposure to 1064 nm near-infrared (NIR) light causes the CaP shell structure to collapse, releasing CuHDB nanozymes and “switching on” their enzyme-like activity. This enables the CuHDB@CaP nanotherapeutic platform to be both safe and highly efficient. CuHDB exhibits not only a strong photothermal effect but also enhanced glutathione oxidase (GSHOx)-like and peroxidase (POD)-like enzyme activities. The GSHOx-like activity contributes to the generation of H2O2, and its excellent H2O2 affinity allows it to efficiently catalyze the conversion of H2O2 to a sufficient amount of •OH through POD-like activity. This self-cascading catalytic platform does not require the introduction of additional H2O2 and also promotes the consumption of GSH in the wound infection microenvironment. CuHDB@CaP can kill up to 99.0% of MRSA and AmprE. coli, effectively inhibit biofilm formation without the emergence of drug resistance, and exhibit negligible cytotoxicity and hemolysis. Treatment experiments in mouse wound infection models showed that CuHDB@CaP combined with NIR could effectively treat wound infections and accelerate wound healing with minimal toxicity to normal tissue cells, demonstrating its potential for the clinical treatment of skin infections.

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Publication Details

Journal
ACS Applied Nano Materials
Published
2024-12-28
DOI
https://doi.org/10.1021/acsanm.4c06225
Citations
2
Primary Topic
Advanced Nanomaterials in Catalysis
Type
article
Field-Weighted Citation Impact
0.23

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article

NIR-II/pH Dual Responsive CuHDB@CaP Nanospheres as a Self-Cascading Catalytic Platform for Highly Efficient Combating Bacterial Infections

Bingyan Li, Wei‐Wei Gao, Zongchao Jia, Fanxiang Meng et al.
2 citations
ACS Applied Nano Materials
Advanced Nanomaterials in Catalysis
0.23
article

NIR-II/pH Dual Responsive CuHDB@CaP Nanospheres as a Self-Cascading Catalytic Platform for Highly Efficient Combating Bacterial Infections

Bingyan Li, Wei‐Wei Gao, Zongchao Jia, Fanxiang Meng, Bo Li, Ya‐Mu Xia, Xue-Yao Pang, Ting Hou
article en
2 citations

Abstract

The misuse of antibiotics has led to a dramatic increase in bacterial resistance, creating an urgent need for efficient antimicrobial agents with multiple mechanisms of action. In this study, Cu was modified with berberine derivatives, and a core–shell structure was successfully developed, resulting in a light/pH-responsive CuHDB@CaP nanotherapeutic platform. It achieves controlled release of CuHDB nanozymes, with CaP, which is highly stable in neutral or alkaline environments, preventing CuHDB leakage and effectively “switching off” the activity of nanozymes. Bacterial metabolism, which produces lactic and keto acids, lowers the pH of the wound microenvironment. Additionally, exposure to 1064 nm near-infrared (NIR) light causes the CaP shell structure to collapse, releasing CuHDB nanozymes and “switching on” their enzyme-like activity. This enables the CuHDB@CaP nanotherapeutic platform to be both safe and highly efficient. CuHDB exhibits not only a strong photothermal effect but also enhanced glutathione oxidase (GSHOx)-like and peroxidase (POD)-like enzyme activities. The GSHOx-like activity contributes to the generation of H2O2, and its excellent H2O2 affinity allows it to efficiently catalyze the conversion of H2O2 to a sufficient amount of •OH through POD-like activity. This self-cascading catalytic platform does not require the introduction of additional H2O2 and also promotes the consumption of GSH in the wound infection microenvironment. CuHDB@CaP can kill up to 99.0% of MRSA and AmprE. coli, effectively inhibit biofilm formation without the emergence of drug resistance, and exhibit negligible cytotoxicity and hemolysis. Treatment experiments in mouse wound infection models showed that CuHDB@CaP combined with NIR could effectively treat wound infections and accelerate wound healing with minimal toxicity to normal tissue cells, demonstrating its potential for the clinical treatment of skin infections.

ACS Applied Nano MaterialsVol. 8(1)
Qingdao University of Science and Technology (CN), State Key Laboratory of Chemical Engineering (CN)
National Natural Science Foundation of China, Natural Science Foundation of Shandong Province
Zero hunger
Openalex Percentile: Top 49%
Advanced Nanomaterials in Catalysis
0.23
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