4.5 Article

The antibacterial and antibiofilm activities of mesoporous hollow Fe3O4 nanoparticles in an alternating magnetic field

Journal

BIOMATERIALS SCIENCE
Volume 8, Issue 16, Pages 4492-4507

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0bm00673d

Keywords

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Funding

  1. National Natural Science Foundation of China [51772233, 51672206]
  2. National Key Research and Development Program of China [2018YFB1105500, 2016YFC1101605]
  3. Major Special Projects of Technological Innovation of Hubei Province [2019ACA130]
  4. Application Foundation and Front research program of Wuhan [2018010401011273]
  5. Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory [XHT2020-008]

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Unrestricted usage of antibiotics has accelerated the emergence of new strains of microorganisms with antimicrobial resistance (AMR) and the development of therapeutic technologies that do not rely only on antibiotics. Herein, mesoporous hollow Fe(3)O(4)nanoparticles (MHFPs) were synthesized by a one-pot hydrothermal method, and the feasibility and possible mechanism of using alternating magnetic field (AMF) with MHFPs to killEscherichia coli(E. coli) andStaphylococcus aureus(S. aureus) were explored. The presence of the AMF (2.5 kW, 210 kHz) combined with the MHFPs resulted in a dramatic decrease in colony forming units (CFU) forE. coliandS. aureusin 25 min compared with the pure MHFPs at concentrations of 500, 800 and 1000 mu g mL(-1). Macroscopic hyperthermia was proved not to be the sole reason for the phenomenon. Visible membrane damage was demonstrated by live/dead staining, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) assays. Besides, the permeability and integrity changes of the cell membrane were then quantitatively confirmed by measuring the relative electrical conductivity. In addition, bacterial biofilms were significantly dispersed in the presence of MHFPs and AMF. These results suggested that under the mediation of AMF, MHFPs can potentially serve as an efficient nonantibiotic therapeutic platform to disperse bacterial biofilms and inactivate bacteria by damaging the cell membrane of the bacteria.

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