研究目的
To study the coating formation mechanism and its chemical composition, as well as the influence of the coatings on a cell culture.
研究成果
The research demonstrates that nitrogen-doped titanium dioxide coatings on PLLA scaffolds enhance biocompatibility, with optimal cell adhesion at 4 minutes of treatment. The coatings transition from organic-inorganic composites to inorganic solid solutions over time. Future work should explore applications on nanofiber scaffolds and further in vivo validation.
研究不足
The study is limited to specific treatment times and conditions; scalability and long-term effects in vivo are not addressed. Potential optimization includes varying more sputtering parameters and testing with other cell types or in vivo models.
1:Experimental Design and Method Selection:
The study used reactive magnetron sputtering to deposit nitrogen-doped titanium dioxide thin films on PLLA electrospun microfibers scaffolds. The methodology included optical spectroscopy, SEM, XPS, DFT calculations, and cell culture assays to analyze the coatings and their effects.
2:Sample Selection and Data Sources:
PLLA scaffolds were produced using a 3 wt% solution of PLLA in trichloromethane via electrospinning with specific parameters. Human umbilical vein endothelial cells (HUVEC) were used for cell interaction studies.
3:List of Experimental Equipment and Materials:
Equipment included a balanced magnetron sputtering system, OCEAN OPTICS HR 2000+ spectrometer, Quanta 200 3D SEM, Escalab 250Xi XPS machine, GuavaEasyCyte8 flow cytometer, CO2 incubator, and Axio Observer fluorescence microscope. Materials included PLLA PL-38, trichloromethane, nitrogen gas, titanium target, and various chemicals for cell culture and staining.
4:Experimental Procedures and Operational Workflow:
Scaffolds were prepared, solvent removed under vacuum, and then treated with magnetron sputtering at different times (2, 4, 6, 8 min). Coatings were characterized using optical spectroscopy, SEM, XPS, and DFT. Cell adhesion and proliferation were assessed through fluorescence microscopy after 72 hours of culture.
5:Data Analysis Methods:
Data were analyzed using SpectraSuite, ImageJ, Origin 9.0, Jaguar software for DFT, and Statistica 7.0 for statistical analysis with one-way ANOVA.
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OCEAN OPTICS HR 2000+
HR 2000+
Ocean Optics
Optical spectroscopy measurement of plasma composition
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Quanta 200 3D
Quanta 200 3D
FEI
Scanning electron microscopy for morphology investigation
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Escalab 250Xi
Escalab 250Xi
Thermo Fisher Scientific
XPS measurements for chemical composition analysis
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Axio Observer
Axio Observer
Carl Zeiss
Fluorescence microscopy for cell analysis
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GuavaEasyCyte8
GuavaEasyCyte8
Millipore
Flow cytometry for cell immunophenotyping
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