研究目的
To address deficient osseointegration and implant-related infections of titanium implants by developing a Zn/Sr-doped titanium dioxide microporous coating via microarc oxidation to enhance osteogenic activity and antibacterial properties.
研究成果
The Zn/Sr-doped coating significantly enhances osteogenic activity and antibacterial properties, promoting early osseointegration in vivo, offering a promising approach for improving titanium implant performance with potential clinical applications.
研究不足
The study may have limitations in terms of the specific conditions of MAO processing, potential variability in coating uniformity, and the use of animal models which may not fully replicate human responses. Optimization could involve scaling up for clinical applications and long-term stability tests.
1:Experimental Design and Method Selection:
The study used microarc oxidation (MAO) to prepare coatings on titanium surfaces, with Zn and Sr doping to enhance biological activity. In vitro and in vivo tests were conducted to evaluate osteogenic and antibacterial effects.
2:Sample Selection and Data Sources:
Pure TA2 titanium samples were used, cut into specific dimensions. MC3T3-E1 preosteoblasts and S. aureus bacteria were cultured for in vitro assays; New Zealand rabbits were used for in vivo studies.
3:List of Experimental Equipment and Materials:
Equipment included a DC pulse power supply for MAO, FE-SEM (HITACHI S-4800), EDS (Bruker), confocal laser scanning microscope, micro-CT, and various kits for assays (e.g., CCK-8, EdU, LIVE/DEAD). Materials included sodium hexametaphosphate, sodium hydroxide, ethylene diamine tetraacetic acid, sodium citrate, Zn gluconate, Sr gluconate, fetal bovine serum, α-MEM, and others.
4:Experimental Procedures and Operational Workflow:
Samples were prepared via MAO, characterized using SEM and EDS, and subjected to protein adsorption, cytotoxicity, cell adhesion, proliferation, differentiation, antibacterial tests, and in vivo implantation in rabbits with subsequent X-ray, micro-CT, and histological analyses.
5:Data Analysis Methods:
Data were analyzed using statistical techniques, with qRT-PCR for gene expression, Western blot for protein analysis, and image analysis for cell and bacterial counts.
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FE-SEM
S-4800
HITACHI
Observing surface morphology of samples
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EDS
Bruker
Analyzing chemical composition of coatings
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DC pulse power supply
Conducting microarc oxidation treatment
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Confocal laser scanning microscope
Olympus
Imaging cellular fluorescence
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Micro-CT
Evaluating peri-implant bone formation
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CCK-8 assay kit
Assessing cell adhesion and proliferation
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EdU proliferation assay kit
Click-iT EdU
Measuring cell proliferation
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LIVE/DEAD viability/cytotoxicity kit
Staining live and dead cells
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qRT-PCR equipment
Quantifying gene expression
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Western blot equipment
Measuring protein expression levels
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