研究目的
To develop a new hybrid nanoplatform integrating diagnosis and treatment elements for effective theranostics of tumors, specifically for multimode imaging and photothermal therapy.
研究成果
The developed ASPP nanoparticles are effective for multimode imaging and photothermal therapy of tumors, with high photothermal conversion efficiency and ability to inhibit metastasis, showing promise for clinical applications.
研究不足
The study may have limitations in scalability of synthesis, potential long-term toxicity not fully explored, and specificity to certain tumor types; optimization could involve targeting ligands for improved specificity.
1:Experimental Design and Method Selection:
The study involved synthesizing Au@mSiO2-PFH-PDA nanoparticles using a sodium citrate reduction method, selective etching, amination, PFH filling, and PDA coating. Theoretical models include photothermal conversion and imaging principles.
2:Sample Selection and Data Sources:
Au seed particles, 4T1 cancer cells, and xenografted tumor models in nude mice were used. Data were acquired through various characterization techniques.
3:List of Experimental Equipment and Materials:
Equipment includes transmission electron microscopy (TEM), scanning electron microscopy (SEM), FTIR spectrometer, TGA analyzer, UV-vis spectrometer, N2 adsorption-desorption analyzer, zeta potential analyzer, PA imaging system, US imaging system, CT scanner, thermal camera, 808 nm laser, cell culture facilities, and animal handling tools. Materials include sodium citrate, polyvinylpyrrolidone (PVP), silica precursors, APTES, PFH, dopamine, tris buffer, PBS, cell culture reagents, and mice.
4:Experimental Procedures and Operational Workflow:
Synthesis steps: Au seed synthesis, coating with PVP, growth of silica shells, etching, amination, PFH filling, PDA coating. Characterization: TEM, SEM, FTIR, TGA, UV-vis, N2 adsorption, zeta potential, colloidal stability tests. In vitro assays: cytotoxicity (CCK-8), cellular uptake, photothermal therapy. In vivo studies: PA, US, CT, thermal imaging, photothermal therapy in tumor models, biodistribution analysis.
5:Data Analysis Methods:
Data were analyzed using statistical methods (e.g., linear regression for imaging signals), software for image analysis, and instruments' built-in analysis tools.
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Transmission Electron Microscopy
Used for imaging and characterizing the morphology and size of nanoparticles.
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Scanning Electron Microscopy
Used for observing the morphology of nanoparticles.
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FTIR Spectrometer
Used for characterizing the chemical structure of nanoparticles.
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TGA Analyzer
Used for thermal gravimetric analysis to quantify material loadings.
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UV-vis Spectrometer
Used for measuring optical absorption properties.
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N2 Adsorption-desorption Analyzer
Used for measuring surface area and pore characteristics.
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Zeta Potential Analyzer
Used for measuring surface charge of nanoparticles.
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Photoacoustic Imaging System
Used for PA imaging of nanoparticles.
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Ultrasound Imaging System
Used for US imaging in B mode.
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CT Scanner
Used for CT imaging.
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Thermal Camera
Used for thermal imaging.
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808 nm Laser
Used for photothermal therapy and imaging.
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Cell Counting Kit-8
CCK-8
Used for cytotoxicity assays.
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