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2D Materials Kill Bacteria from Within.
Hou, Delong; Zhou, Shuai; Tan, Xueling; Yuan, Dongzhi; Yan, Jun; Zeng, Qi; Chen, Yi.
Afiliación
  • Hou D; College of Biomass Science and Engineering, Sichuan University, Chengdu 610065, P. R. China.
  • Zhou S; College of Biomass Science and Engineering, Sichuan University, Chengdu 610065, P. R. China.
  • Tan X; College of Biomass Science and Engineering, Sichuan University, Chengdu 610065, P. R. China.
  • Yuan D; West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University, Chengdu 610065, P. R. China.
  • Yan J; College of Biomass Science and Engineering, Sichuan University, Chengdu 610065, P. R. China.
  • Zeng Q; College of Biomass Science and Engineering, Sichuan University, Chengdu 610065, P. R. China.
  • Chen Y; College of Biomass Science and Engineering, Sichuan University, Chengdu 610065, P. R. China.
Nano Lett ; 24(22): 6506-6512, 2024 Jun 05.
Article en En | MEDLINE | ID: mdl-38789389
ABSTRACT
Early work demonstrated that some two-dimensional (2D) materials could kill bacteria by using their sharp edges to physically rupture the bacteria envelope, which presents distinct advantages over traditional antibiotics, as bacteria are not able to evolve resistance to the former. This mechano-bactericidal mode of action, however, suffers from low antibacterial efficiency, fundamentally because of random orientation of 2D materials outside the bacteria, where the desirable "edge-to-envelope" contacts occur with low probability. Here, we demonstrate a proof-of-concept approach to significantly enhance the potency of the mechano-bactericidal activity of 2D materials. This approach is in marked contrast with previous work, as the 2D materials are designed to be in situ generated inside the bacteria from a molecularly engineered monomer in a self-assembled manner, profoundly promoting the probability of the "edge-to-envelope" contacts. The rationale in this study sheds light on a mechanically new nanostructure-enabled antibacterial strategy to combat antibiotic resistance.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Nanoestructuras / Antibacterianos Idioma: En Revista: Nano Lett Año: 2024 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Nanoestructuras / Antibacterianos Idioma: En Revista: Nano Lett Año: 2024 Tipo del documento: Article