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Facile green synthesis of silver nanoparticles derived from the medicinal plant and its biological activity against species. | LitMetric

AI Article Synopsis

  • The rise of multidrug-resistant mycobacteria poses a serious challenge in treating tuberculosis, leading to treatment failures and reliance on more toxic, expensive medications.
  • This study investigates the use of green-synthesized silver nanoparticles (AgNPs) and their polyethylene glycol encapsulated version (PEG-AgNPs) as potential novel antimicrobials, demonstrating that PEG-AgNPs have better stability and enhanced anti-mycobacterial activity.
  • Characterization techniques revealed the uniform size and stability of PEG-AgNPs, and their effectiveness was shown through increased cell wall permeability and significant biofilm inhibition, along with a lack of toxicity towards human red blood cells.

Article Abstract

The emergence of multidrug-resistant mycobacterial strains is a significant crisis that has led to higher treatment failure rates and more toxic and expensive medications for tuberculosis (TB). The urgent need to develop novel therapeutics has galvanized research interest towards developing alternative antimicrobials such as silver nanoparticles (AgNPs). The current study focused on the anti-mycobacterial activity of green-synthesized AgNPs and its polyethylene glycol encapsulated derivative (PEG-AgNPs) with improved stability using the leaves extract of . Different characterization methods were used to analyze them. DLS analysis revealed a lower polydispersity index of PEG-AgNPs, suggesting a more uniform size distribution than that of AgNPs. The HR-TEM results revealed that the AgNPs and PEG-AgNPs have predominantly spherical shapes in the size range of 9-35 nm and 15-60 nm, respectively, while positive values of Zeta potential indicate their stability. FTIR-ATR analysis confirmed the presence of functional groups responsible for reducing and capping the bio-reduced AgNPs, whereas the XRD data established its crystalline nature. Impressively, the PEG-AgNPs exhibited maximum inhibitory activity against different Tubercular and Non-Tuberculous species , and , relative to those of AgNPs and Linezolid. The flow cytometry assay showed that the anti-mycobacterial action was mediated by an increase in cell wall permeability. Notably, the results of AFM confirm their ability to inhibit mycobacterial biofilm significantly. We demonstrated the nontoxic nature of these AgNPs, explicated by the absence of hemolytic activity against human RBCs. Overall, the results suggest that PEG-AgNPs could offer a novel therapeutic approach with potential anti-mycobacterial activity and can overcome the limitations of existing TB therapies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11126841PMC
http://dx.doi.org/10.1016/j.heliyon.2024.e31116DOI Listing

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