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DOI 10.1039/c6nr01243d

Медицинская библиотека · Nanoscale · 2016

Versatile molybdenum disulfide based antibacterial composites for in vitro enhanced sterilization and in vivo focal infection therapy.

Zhang Wentao, Shi Shuo, Wang Yanru, Yu Shaoxuan, Zhu Wenxin, Zhang Xu, Zhang Daohong, Yang Baowei, Wang Xin, Wang Jianlong

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Аннотация

Biologically, MoS2-based nanostructures have been intensely applied for the photothermal therapy of cancer, but rarely for antibacterial uses. In this contribution, a multifunctional chitosan (CS) functionalized magnetic MoS2 (abbreviated to CFM) was constructed to nonspecifically combat bacterial infection by integrating bacterial conjugation and enrichment, and NIR-triggered photothermal sterilization. Owing to the abundant introduced amino groups, the CFM complex offers a significantly enhanced conjugation efficiency without obvious specificity towards both Gram-positive and -negative bacteria compared to amino-free magnetic MoS2. The magnetic properties of CFM obtained from iron oxide facilitate the enrichment of a CFM-bacteria conjugate, improving the photothermal efficiency of CFM as a photothermal antibacterial agent. Specifically, after being trapped together with bacteria cells, CFM shows an enhanced in vitro photothermal sterilization ability. In vivo S. aureus-induced abscess treatment studies show faster healing when CFM is used as subcutaneous nano-localized heating sources with the assistance of an external magnet to concentrate the CFM-bacteria conjugate. This work establishes an innovative solution and a novel antimicrobial agent for combating bacterial infections without the use of antibiotics, which may open a new area of application and research for MoS2-based nanostructures.

Для цитирования: Zhang Wentao, Shi Shuo, Wang Yanru, Yu Shaoxuan, Zhu Wenxin, Zhang Xu, Zhang Daohong, Yang Baowei, Wang Xin, Wang Jianlong. Versatile molybdenum disulfide based antibacterial composites for in vitro enhanced sterilization and in vivo focal infection therapy.. Nanoscale. 2016. DOI: 10.1039/c6nr01243d.

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