4.7 Article Proceedings Paper

Combination of Silver Nanoparticles and Curcumin Nanoparticles for Enhanced Anti-biofilm Activities

期刊

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
卷 64, 期 12, 页码 2513-2522

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jafc.5b04559

关键词

nanoparticles; Pseudomonas aeruginosa; biofilm; Staphylococcus aureus; combination therapy

资金

  1. NHMRC Senior Research Fellowship [571905]
  2. Australian Research Council Future Fellowship [FT110100996, FT12010063]
  3. National Health and Medical Research Council of Australia [571905] Funding Source: NHMRC

向作者/读者索取更多资源

Biofilm tolerance has become a serious clinical concern in the treatment of nosocomial pneumonia owing to the resistance to various, antibiotics. There is an urgent need to develop alternative antimicrobial agents or combination drug therapies that are effective via different mechanisms. Silver nanoparticles (AgNPs) have been developed as an anti-biofilm agent for the treatment of infections associated with the use of mechanical ventilations, such as endotracheal intubation. Meanwhile curcumin, a phenolic plant extract, has displayed natural anti-biofilm properties through the inhibition of bacterial quorum sensing systems. The aim Of this study was to investigate the possible synergistic/additive interactions of AgNPs and curcumin nanopattides (Cur-NPs) against both Gram-negative,(Pseudomonas aeruginosa) and Gram-positive (Staphylococcus aureus) microorganisms. The combination of AgNPs and Cur-NPs (termed Cur-SNPs) at 100 mu g/mL disrupted 50% of established bacterial biofilms (formed on mcrotiter plates). However, further increase in the concentration of Cur-SNPs failed to effectively eliminate the biofilms. To achieve the same effect, at least 500 mu g/mL Cur-NP alone was needed. Scanning electron microscopy (SEM) and confocal laser scanning microscopy (CLSM) revealed that combination therapy.(Cur-SNPs) was the most potent to eradicate preformed biofilm compared to monodrug therapy. These agents are also nontoxic to healthy human bronchial epithelial cells (BEAS2B).

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