研究目的
Investigating the photodynamic antimicrobial properties of naked gold nanoparticles under low-power density continuous wave laser irradiation for inactivating Escherichia coli, to address the gap in existing research and explore potential for localized pathogen inactivation with minimal side effects.
研究成果
The synergistic use of low-power density laser and naked gold nanoparticles effectively inactivates E. coli through photodynamic mechanisms without significant temperature rise, indicating potential for targeted antimicrobial applications with minimal tissue damage. This approach offers a promising alternative to high-power lasers and antibiotics, warranting further research on optimization and broader applicability.
研究不足
The study used a specific strain of E. coli and low-power laser; results may not generalize to other bacteria or higher power settings. Aggregation of nanoparticles in ionic media could affect efficiency, and the mechanism of singlet oxygen generation requires further validation. Future work could optimize laser parameters and nanoparticle properties.
1:Experimental Design and Method Selection:
The study aimed to evaluate the synergistic effects of low-power density laser light and naked gold nanoparticles on bacterial inactivation. Methods included photodynamic inactivation assays, singlet oxygen detection using DPBF bleaching, and characterization of nanoparticles.
2:Sample Selection and Data Sources:
Escherichia coli ATCC 25922 was used as the model microorganism. Gold nanoparticles were purchased from PNF company, and various concentrations were prepared by dilution.
3:List of Experimental Equipment and Materials:
Equipment included a TEM microscope (Philips CM30), DLS instrument (Cordouan Technology), UV-visible spectrophotometer (Spekol 2000, Analyticjena CO), CW Nd:Yag laser (CNI Laser, model MGL-III-532), beam expander, infrared thermometer, shaker incubator (FF-81, ParsAzma Co.), and statistical software (SigmaPlot 12.0). Materials included gold nanoparticles, DPBF (Sigma-Aldrich), nutrient broth, saline solution, and deionized water.
4:0). Materials included gold nanoparticles, DPBF (Sigma-Aldrich), nutrient broth, saline solution, and deionized water. Experimental Procedures and Operational Workflow:
4. Experimental Procedures and Operational Workflow: Gold nanoparticles were characterized using TEM and DLS. Singlet oxygen generation was assessed by monitoring DPBF absorbance changes under laser illumination. Bacterial cultures were prepared and exposed to laser light with and without gold nanoparticles at various concentrations and exposure times. Viability was assessed through colony counting after serial dilution and incubation.
5:Data Analysis Methods:
Statistical analysis was performed using one-way ANOVA and Tukey post hoc test with SigmaPlot software, considering results with P < 0.05 as significant.
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UV-visible Spectrophotometer
Spekol 2000
Analyticjena CO
Used to obtain absorption spectra of samples, including gold nanoparticles and DPBF solutions.
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Laser
MGL-III-532
CNI Laser
Used as the light source for illumination experiments, specifically a CW second harmonic Nd:Yag laser at 532 nm.
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Transmission Electron Microscope
CM30
Philips
Used for TEM studies to characterize the size and morphology of gold nanoparticles.
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Dynamic Light Scattering Instrument
Cordouan Technology
Used for DLS measurements to determine the size distribution of gold nanoparticles.
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Infrared Thermometer
Used to measure the temperature of solutions during light illumination to monitor thermal effects.
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Shaker Incubator
FF-81
ParsAzma Co.
Used for culturing bacteria under controlled conditions of temperature and agitation.
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Gold Nanoparticles
PNF (Payamavaran Nanofanavari Fardanegar)
Used as the photosensitizing agent in photodynamic inactivation experiments.
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DPBF
Sigma-Aldrich
Used as a singlet oxygen scavenger to detect singlet oxygen generation during laser illumination.
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