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硫化铜纳米组装体用于催化和光响应消除感染伤口中的细菌。

Copper Sulfide Nanoassemblies for Catalytic and Photoresponsive Eradication of Bacteria from Infected Wounds.

机构信息

Institute of Physics, Academia Sinica, Taipei 11529, Taiwan.

Nano Science and Technology Program, Taiwan International Graduate Program, Institute of Physics, Academia Sinica, Taipei 11529, Taiwan.

出版信息

ACS Appl Mater Interfaces. 2021 Feb 24;13(7):7865-7878. doi: 10.1021/acsami.0c18999. Epub 2021 Feb 15.

DOI:10.1021/acsami.0c18999
PMID:33586966
Abstract

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 (HO) led to the 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 -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 HO at the infection site into hydroxyl radicals and thus increasing the synergistic effect from photodynamic and photothermal treatment. The BSA-CuS NCs exhibited insignificant cytotoxicity and hemolysis and thus can serve as highly biocompatible bactericides in preclinical applications to effectively eradicate bacteria.

摘要

牛血清白蛋白(BSA)包裹的硫化铜纳米晶体(CuS NCs)是通过在不含额外硫源的碱性溶液中加热铜离子和 BSA 而制备的。在高 BSA 浓度(0.8 mM)下,由于 BSA 凝胶状结构的形成,形成的 CuS NCs 会发生纳米组装,从而形成 BSA-CuS NCs。除了它们的固有光热性质外,BSA-CuS NCs 具有丰富的表面空位,因此表现出酶样和光动力活性。过氧化氢(HO)的自发产生导致在 BSA-CuS NCs 上形成过氧化铜(CPO)纳米点,以催化单线态氧自由基的生成。近红外激光照射后,抗菌反应增强了 >60 倍,这归因于细菌的光动力和光热失活的协同作用。此外,BSA-CuS NCs 经皮给药到耐甲氧西林感染的伤口上,在近红外光照射下仅 1 分钟内就消除了 >99%的细菌,这是由于 BSA-CuS NCs 的过氧化物酶样活性将感染部位的 HO 转化为羟基自由基,从而增加了光动力和光热治疗的协同作用。BSA-CuS NCs 表现出不显著的细胞毒性和溶血作用,因此可以作为临床前应用中高度生物相容的杀菌剂,有效地消除细菌。

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