研究目的
Investigating the repression of melanoma tumor in vitro and in vivo by the photothermal effect of carbon xerogel nanoparticles.
研究成果
CX-NPs demonstrated effective photothermal conversion and significant tumor repression in both in vitro and in vivo models, with high necrosis rates and tumor shrinkage. They showed biocompatibility at low doses and are a promising novel agent for photothermal therapy of cancer, particularly melanoma.
研究不足
The study used specific cell lines and animal models, which may not fully represent human melanoma. The laser power and nanoparticle concentrations were fixed, and potential long-term toxicity or side effects were not extensively evaluated. Optimization of synthesis and treatment parameters could be further explored.
1:Experimental Design and Method Selection:
The study involved synthesizing carbon xerogel nanoparticles (CX-NPs) and evaluating their photothermal properties for cancer therapy. Methods included sol-gel synthesis, characterization using electron microscopy, and in vitro and in vivo assays to assess cytotoxicity and tumor inhibition.
2:Sample Selection and Data Sources:
Mouse malignant melanoma C540 (B16/F10) cells and male balb/c mice were used. Cells were cultured in RPMI-1640 medium, and mice were implanted with tumor cells subcutaneously.
3:List of Experimental Equipment and Materials:
Equipment included a Zeiss Sigma-IGMA/VP FESEM microscope, Zeiss-EM10C TEM microscope, Rayleigh UV-2601 spectrophotometer, Thorlabs diode laser system, Lutron thermoprobe, Biotek microplate reader, and Olympus microscope. Materials included cathechol, formaldehyde, ethanol, HCl, MTT, DMSO, ketamin, xylazine, and various chemicals from Sigma, Scharlau, and Merck.
4:Experimental Procedures and Operational Workflow:
Synthesis of CX-NPs via sol-gel process and carbonization. Characterization by UV-vis, FESEM, and TEM. Photothermal testing with laser irradiation. In vitro cytotoxicity using MTT assay on cells treated with CX-NPs and laser. In vivo studies on tumor-bearing mice with intratumoral injections and laser irradiation, followed by tumor volume measurement and histological analysis.
5:Data Analysis Methods:
Statistical analysis using Kruskal-Wallis test and t-test with GraphPad Prism 6 software; p<0.05 considered significant.
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FESEM microscope
Sigma-IGMA/VP
Zeiss
Characterization of nanoparticle size and morphology
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TEM microscope
EM10C
Zeiss
Characterization of nanoparticle size and morphology
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UV-vis spectrophotometer
UV-2601
Rayleigh
Recording UV-vis spectra of nanoparticles
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Diode laser system
Thorlabs
Irradiation with 808-nm laser light for photothermal therapy
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Thermoprobe
Lutron
Recording temperature changes during laser irradiation
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Microplate reader
Biotek
Measuring absorbance for MTT assay to determine cell viability
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Microscope
Olympus
Histological analysis of stained tissue slides
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