4.8 Article

Bactericidal Effect of Gold-Chitosan Nanocomposites in Coculture Models of Pathogenic Bacteria and Human Macrophages

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 9, 期 21, 页码 17693-17701

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.6b15123

关键词

bactericidal nanomaterials; infection; nanocomposites; chitosan; gold nanoparticles

资金

  1. EU [ERC-2013-CoG-614715]
  2. National Science Centre Poland [2012/07/N/STS/00157]
  3. VI National R&D&i Plan, Iniciativa Ingenio, Consolider Program, CIBER Actions
  4. Instituto de Salud Carlos III (Spain)
  5. European Regional Development Fund

向作者/读者索取更多资源

The ability of pathogenic bacteria to develop resistance mechanisms to avoid the antimicrobial potential of antibiotics has become an increasing problem for the healthcare system. The search for more effective and selective antimicrobial materials, though not harmful to mammalian cells, seems imperative. Herein we propose the use of gold-chitosan nanocomposites as effective bactericidal materials avoiding damage to human cells. Nanocomposites were obtained by taking advantage of the reductive and stabilizing action of chitosan solutions on two different gold precursor concentrations. The resulting nanocomposites were added at different final concentrations to a coculture model formed by Gram-positive (Staphylococcus aureus) or Gram-negative (Escherichia coli) bacteria and human macrophages. Gold chitosan colloids exhibited superior bactericidal ability against both bacterial models without showing cytotoxicity on human cells at the concentrations tested. Morphological and in vitro viability studies supported the feasibility of the infection model here described to test novel bactericidal nanomaterials. Flow cytometry and scanning electron microscopy analyses pointed to the disruption of the bacterial wall as the lethal mechanism. Data obtained in the present study suggest that gold chitosan nanocomposites are powerful and promising nanomaterials for reducing bacteria associated infections, respecting the integrity of mammalian cells, and displaying high selectivity against the studied bacteria.

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