AI Article Synopsis

  • * The research aimed to evaluate the antimicrobial effectiveness of Ag-NPs, various APs individually, and their combinations, using methods like UV-visible spectra and electron microscopy for characterization.
  • * Findings indicated that combining Ag-NPs with certain APs improved antimicrobial activity and biofilm eradication, suggesting these nanocomplexes could be promising candidates for future treatments of microbial infections.

Article Abstract

Antimicrobial resistance has become a major problem over the years and threatens to remain in the future, at least until a solution is found. Silver nanoparticles (Ag-NPs) and antimicrobial polymers (APs) are known for their antimicrobial properties and can be considered an alternative approach to fighting resistant microorganisms. Hence, the main goal of this research is to shed some light on the antimicrobial properties of Ag-NPs and APs (chitosan (CH), poly-L-lysine (PLL), ε-poly-L-lysine (ε-PLL), and dopamine (DA)) when used alone and complexed to explore the potential enhancement of the antimicrobial effect of the combination Ag-NPs + Aps. The resultant nanocomplexes were chemically and morphologically characterized by UV-visible spectra, zeta potential, transmission electron microscopy, and Fourier-transform infrared spectroscopy. Moreover, the Ag-NPs, APs, and Ag-NPs + APs nanocomplexes were tested against Gram-positive () and the Gram-negative () bacteria, as well as the fungi (). Overall, the antimicrobial results showed potentiation of the activity of the nanocomplexes with a focus on . For the biofilm eradication ability, Ag-NPs and Ag-NPs + DA were able to significantly remove preformed biofilm, and Ag-NPs + CH were able to significantly destroy biofilm, with both performing better than Ag-NPs alone. Overall, we have proven the successful conjugation of Ag-NPs and APs, with some of these formulations showing potential to be further investigated for the treatment of microbial infections.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10815966PMC
http://dx.doi.org/10.3390/ijms25021256DOI Listing

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