Synthesized uniform-different sizes silver nanoparticles using TSC and SBH simultaneously for antibacterial
1Thai Nguyen University of Education, No. 20, Luong Ngoc Quyen Street, Quang Trung Ward, Thai Nguyen City, Vietnam.
Biomedical Physics & Engineering Express
|January 18, 2024
Summary
This study synthesized silver nanoparticles (AgNPs) using two reducing agents, finding smaller sizes and 50 μg/ml concentrations exhibit superior antibacterial activity against resistant bacteria.
Area of Science:
- Nanotechnology
- Materials Science
- Microbiology
Background:
- Silver nanoparticles (AgNPs) exhibit potent antimicrobial properties.
- Controlling AgNP size and synthesis is crucial for optimizing antibacterial efficacy.
- Investigating AgNP interactions with resistant bacterial strains is essential for developing new treatments.
Purpose of the Study:
- To synthesize uniform silver nanoparticles (AgNPs) using a novel dual-reducing agent method.
- To evaluate the impact of AgNP size and concentration on antibacterial activity.
- To compare the efficacy of AgNPs against *Pseudomonas aeruginosa* (PA) and *Staphylococcus aureus* (SA).
Main Methods:
- Controlled synthesis of AgNPs using sodium borohydride (SBH) and trisodium citrate (TSC).
- Characterization of AgNPs using Transmission Electron Microscopy (TEM) and Dynamic Light Scattering (DLS).
- Antimicrobial activity assessed via the disc diffusion method against PA and SA.
Main Results:
- Antibacterial activity of AgNPs is dependent on concentration and particle size.
- Optimal antibacterial effect observed at 50 μg/ml concentration.
- Smaller AgNPs demonstrated significantly higher antibacterial efficacy.
- The dual-reducing agent method yielded uniform AgNPs, enhancing antibacterial performance.
Conclusions:
- The simultaneous use of TSC and SBH enables controlled synthesis of uniform AgNPs.
- Smaller AgNPs exhibit enhanced antibacterial properties against *P. aeruginosa* and *S. aureus*.
- Optimized AgNP concentration and size present a promising strategy for combating resistant bacterial infections.
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