4.7 Article

Synthesis and characterization of chitosan silver nanoparticle decorated with benzodioxane coupled piperazine as an effective anti-biofilm agent against MRSA: A validation of molecular docking and dynamics

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ELSEVIER
DOI: 10.1016/j.ijbiomac.2021.03.119

关键词

Biofilm; Biocompatibility; Piperazine; Silver nanoparticle; Chitosan

资金

  1. VGST, GoK [647]

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This study synthesized benzodioxane coupled piperazine decorated chitosan silver nanoparticles (Bcp*C@AgNPs) and evaluated its antibacterial and anti-biofilm properties against methicillin-resistant Staphylococcus aureus (MRSA). The nanoparticles showed effective antibacterial activity and a reduced toxic effect on myoblast cells.
Biomaterial research has improved the delivery and efficacy of drugs over a wide range of pharmaceutical applications. The objective of this study was to synthesize benzodioxane coupled piperazine decorated chitosan silver nanoparticle (Bcp*C@AgNPs) against methicillin-resistant Staphylococcus aureus (MRSA) and to assess the nano particle as an effective candidate for antibacterial and anti-biofilm care. Antibacterial activity of the compound was examined and minimum inhibitory concentration (MIC) was observed at (10.21 +/- 0.03 ZOI) a concentration of 200 mu g/mL. The Bcp*C@AgNPs interferes with surface adherence of MRSA, suggesting an anti-biofilm distinctive property that is verified for the first time by confocal laser microscopic studies. By ADMET studies the absorption, distribution, metabolism, excretion and toxicity of the compound was examined. The interaction solidity and the stability of the compound when surrounded by water molecules were analyzed by docking and dynamic simulation analysis. The myoblast cell line (L6) was considered for toxicity study and was observed that the compound exhibited less toxic effect. This current research highlights the biocidal efficiency of Bcp*C@AgNPs with their bactericidal and anti-biofilm properties over potential interesting clinical trial targets in future. (c) 2021 Elsevier B.V. All rights reserved.

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