研究目的
To study the effect of anisotropic gold nanoparticles on plasmonic coupling with a photosensitizer for antimicrobial film development, aiming to produce a steady and efficient killing of bacteria under light exposure.
研究成果
The films containing anisotropic gold nanoparticles and crystal violet dye showed significant antimicrobial activity against both gram negative and positive bacteria under light exposure, with AuNSs showing higher efficiency in ROS production and bacterial reduction. The differential response of gram (-) and gram (+) bacteria to ROS suggests potential for targeted antimicrobial surfaces. The study highlights the importance of plasmonic coupling between nanoparticles and dye for enhancing antimicrobial activity.
研究不足
The study focuses on specific types of bacteria (E. coli and S. aureus) and may not cover the full spectrum of bacterial resistance mechanisms. The long-term stability and reusability of the antimicrobial films under continuous light exposure were not extensively studied.
1:Experimental Design and Method Selection:
The study involved the synthesis of gold nanorods (AuNRs) and gold nanostars (AuNSs), their characterization, and embedding into a polyurethane (PU) film alongside crystal violet dye (CV) to create antimicrobial surfaces. The surface plasmon resonance (SPR) of the nanoparticles was simulated to understand their interaction with the dye.
2:Sample Selection and Data Sources:
E. coli and S. aureus were used as model gram negative and positive bacteria, respectively.
3:List of Experimental Equipment and Materials:
Instruments included a Philips CM300 FEG TEM for TEM imaging, a Biotek Synergy 2 plate reader for UV-visible spectra, and a Mikro 220R Hettich centrifuge for centrifugation. Materials included HAuCl4, CTAB, NaBH4, AgNO3, L-ascorbic acid, sodium citrate, thiol-PEG-OMe, and polyurethane film.
4:Experimental Procedures and Operational Workflow:
The nanoparticles were synthesized, characterized, and embedded into PU films. The films were then tested for antimicrobial activity against E. coli and S. aureus under light exposure. ROS production was estimated using sodium fluorescein.
5:Data Analysis Methods:
The antimicrobial activity was assessed by counting colonies formed by surviving bacteria. ROS production was quantified using the Stern-Volmer equation and a calibration curve with H2O2.
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