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Copper sulfide nanoassemblies for catalytic and photoresponsive eradication of bacteria from infected wounds
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Copper sulfide nanoassemblies for catalytic and photoresponsive eradication of bacteria from infected wounds

Amit Nain, Shih-Chun Wei, Yu-Feng Lin, Yu-Ting Tseng, Ranju Prasad Mandal, Yu-Fen Huang, Chih-Ching Huang, Fan-Gang TsengHuan-Tsung Chang
ACS Applied Materials and Interfaces, 卷.13(7), 頁碼.7865-7878
02/2021
PMID: 33586966

摘要

Copper peroxide nanodots Copper sulfide nanoassemblies Photoresponsive agents Proteins Reactive oxygen species Wound infection Materials Science (all)
Bovine serum albumin (BSA)-encapsulated copper sulfide nanocrystals (CuS NCs) were prepared by heating an alkaline solution containing copper ions and BSA without an additional sulfur source. At a high BSA concentration (0.8 mM), nanoassembly of the as-formed CuS NCs occurs to form BSA−CuS NCs as a result of the formation of BSA gel-like structures. In addition to their intrinsic photothermal properties, the BSA−CuS NCs possess rich surface vacancies and thus exhibit enzyme-like and photodynamic activities. Spontaneous generation of hydrogen peroxide (H <sub>2</sub> O <sub>2</sub> ) led to the in situ formation of copper peroxide (CPO) nanodots on the BSA−CuS NCs to catalyze singlet oxygen radical generation. The antimicrobial response was enhanced by >60-fold upon NIR laser irradiation, which was ascribed to the combined effect of the photodynamic and photothermal inactivation of bacteria. Furthermore, BSA−CuS NCs were transdermally administered onto a methicillin-resistant Staphylococcus aureus-infected wound and eradicated >99% of bacteria in just 1 min under NIR illumination due to the additional peroxidase-like activity of BSA−CuS NCs, transforming H <sub>2</sub> O <sub>2</sub> at the infection site into hydroxyl radicals and thus increasing the synergistic effect from photodynamic and photothermal treatment. The BSA−CuS NCs exhibited insignificant in vitro cytotoxicity and hemolysis and thus can serve as highly biocompatible bactericides in preclinical applications to effectively eradicate bacteria.

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