研究目的
Investigating the controlled synthesis of triangular silver nanoplates using a gelatin–chitosan mixture and evaluating their antibacterial activity against Gram-positive and Gram-negative bacteria.
研究成果
Triangular silver nanoplates with controlled edge lengths were successfully synthesized using a gelatin–chitosan mixture. The nanoplates exhibited enhanced antibacterial activity compared to spherical silver nanoparticles, with lower MIC and MBC values against Gram-positive and Gram-negative bacteria. The study provides insights into the role of nanoparticle morphology and stabilizing agents in antibacterial applications.
研究不足
The study is limited to the synthesis and characterization of triangular silver nanoplates and their antibacterial activity. The scalability of the synthesis process and the long-term stability of the nanoplates in various environments were not explored.
1:Experimental Design and Method Selection:
The synthesis of triangular silver nanoplates was carried out using a seeding growth approach with citrate-stabilized silver seeds and a gelatin–chitosan mixture as the protecting agent. The synthesis process was optimized by varying experimental parameters such as AgNO3 volume, gelatin–chitosan concentration ratios, and pH conditions.
2:Sample Selection and Data Sources:
Silver seeds were prepared using sodium borohydride as a reducing agent. The growth of triangular silver nanoplates was achieved by adding silver nitrate to a mixture of gelatin–chitosan, H2O2, and ascorbic acid.
3:List of Experimental Equipment and Materials:
Silver nitrate (AgNO3), trisodium citrate (Na3C6H5O7.3H2O), H2O2, sodium borohydride (NaBH4), gelatin (Type B from porcine skin), L (+)-Ascorbic acid (C6H8O6), and chitosan were used. Equipment included transmission electron microscopy (TEM), dynamic light scattering (DLS), UV-Vis spectrophotometer, Fourier transform infrared spectroscopy (FT-IR), and X-Ray diffraction (XRD).
4:3H2O), H2O2, sodium borohydride (NaBH4), gelatin (Type B from porcine skin), L (+)-Ascorbic acid (C6H8O6), and chitosan were used. Equipment included transmission electron microscopy (TEM), dynamic light scattering (DLS), UV-Vis spectrophotometer, Fourier transform infrared spectroscopy (FT-IR), and X-Ray diffraction (XRD). Experimental Procedures and Operational Workflow:
4. Experimental Procedures and Operational Workflow: The synthesis involved the preparation of silver seeds, followed by the growth of triangular silver nanoplates in the presence of a gelatin–chitosan mixture. The process was monitored by observing color changes in the colloidal dispersion.
5:Data Analysis Methods:
The synthesized nanoplates were characterized using TEM, DLS, UV-Vis, FT-IR, and XRD. Antibacterial activity was evaluated using the disk diffusion method and by determining the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC).
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Gelatin
Type B from porcine skin
Sigma-Aldrich
Protecting agent for silver nanoplates
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UV-Vis spectrophotometer
UV-Vis-NIR-V670
JASCO
Characterization of silver nanoplates
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Silver nitrate
AgNO3
Merck
Precursor for the synthesis of silver nanoplates
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Trisodium citrate
Na3C6H5O7.3H2O
Merck
Stabilizing agent for silver seeds
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Sodium borohydride
NaBH4
Merck
Reducing agent for silver seeds
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L (+)-Ascorbic acid
C6H8O6
Prolabo
Reducing agent
-
Chitosan
Protecting agent for silver nanoplates
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Transmission electron microscopy
JEM-1400
Japan
Characterization of silver nanoplates
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Dynamic light scattering
SZ-100
Horiba
Characterization of silver nanoplates
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Fourier transform infrared spectroscopy
Characterization of silver nanoplates
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X-Ray diffraction
D8 Advance-Bruker
Germany
Characterization of silver nanoplates
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