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微弧氧化生物活性TiO_2基纳米结构表面磷灰石诱导能力与药物上载及释放 被引量:3

Apatite formation and drug release ability of nanostructure modified bioactive TiO_2 based microarc oxidation coatings
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摘要 钛因优异的力学性能及良好的生物相容性而被用于代骨生物材料,但其生物惰性限制了它的进一步应用。对钛表面进行微弧氧化-水热改性处理生成复合涂层,可以有效提高钛材的生物活性。本文以Ca(H2PO4)2+Ca(CH3COO)2+EDTA-2Na+NaOH为电解液,在纯钛表面制备TiO2基含钙磷微弧氧化涂层(CP),再经后续水热处理改性,得到具有纳米结构的复合改性涂层;通过模拟体液浸泡实验,以研究不同表面结构复合涂层的磷灰石诱导能力。采用X射线衍射、扫描电子显微镜、X射线光电子谱和傅里叶变换红外光谱手段对试样进行详细分析。结果表明,经过水热处理的微弧氧化涂层较CP涂层表现出更好的生物活性,微弧氧化-水热涂层在模拟体液中浸泡3d均能在涂层表面长满磷灰石。此外,为解决植入体导致的炎症问题,进一步分析了涂层表面上载抗生素药物及其缓释机制。 Ti was used as the generation bone biological material for its excellent biocompaticility and mechanical properties.How-ever,it exhibits bioinert which limits its further application.A composite layer with good bioactivity can be fabricated on the Ti substrate material using a hybrid technique of micro-arc oxidation and hydrothermal treatment to promote its further application. Ca(H2 PO4 )2+Ca(CH3 COO)2+EDTA-2Na+NaOH were used as electrolyte to form TiO2 based MAO coatings containing Ca and P on the substrate.And then the composite layer with nanostructure can be obtained through hydrothermal treatment.SBF immersion was conducted on the samples to investigate the effect of nanostructure on the hydroxyapatite (HA)formation ability of the samples.X-ray diffraction (XRD),scanning electron microscopy (SEM),X-ray photoelectron spectroscopy (XPS)and Fourier transform infrared spectroscopy (FTIR)have been used to analyze the results.The results indicated that the hybrid tech-nique can improve the HA formation ability effectively,and HA can be observed on the composite layer only after 3 days.In addi-tion,to overcome the inflammation resulted from implants,drug coating technique was used to deposit antibacterial drugs on im-plant.
出处 《中国科技论文》 CAS 北大核心 2014年第2期183-186,191,共5页 China Sciencepaper
基金 高等学校博士学科点专项科研基金资助项目(20102302120003) 国家自然科学基金资助项目(51002039 51021002) 国家基础科学研究计划资助项目(2012CB933900)
关键词 涂层 二氧化钛 纳米结构 微弧氧化 水热合成 载药释放 磷灰石 coatings titanium dioxide nanostructures microarc oxidation hydrothermal synthesis drug release apatite
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参考文献8

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