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In vitro apatite formation and drug loading/release of porous TiO2 microspheres prepared by sol-gel processing with different SiO2 nanoparticle contents

机译:溶胶-凝胶法制备不同SiO2纳米颗粒含量的多孔TiO2微球的体外磷灰石形成及载药/释放

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摘要

Bioactive titania (TiO2) microparticles can be used as drug-releasing cement fillers for the chemotherapeutic treatment of metastatic bone tumors. Porous anatase-type TiO2 microspheres around 15 μm in diameter were obtained through a sol–gel process involving a water-in-oil emulsion with 30:70 SiO2/H2O weight ratio and subsequent NaOH solution treatment. The water phase consisted of methanol, titanium tetraisopropoxide, diethanolamine, SiO2 nanoparticles, and H2O, while the oil phase consisted of kerosene, Span 80, and Span 60. The resulting microspheres had a high specific surface area of 111.7 m2·g− 1. Apatite with a network-like surface structure formed on the surface of the microspheres within 8 days in simulated body fluid. The good apatite-forming ability of the microspheres is attributed to their porous structure and the negative zeta potential of TiO2. The release of rhodamine B, a model for a hydrophilic drug, was rapid for the first 6 h of soaking, but diffusion-controlled thereafter. The burst release in the first 6 h is problematic for clinical applications; nonetheless, the present results highlight the potential of porous TiO2 microspheres as drug-releasing cement fillers able to form apatite.
机译:生物活性二氧化钛(TiO2)微粒可用作用于转移性骨肿瘤的化学治疗的药物释放水泥填充剂。通过溶胶-凝胶工艺获得了直径约15μm的多孔锐钛矿型TiO2微球,该工艺涉及SiO2 / H2O重量比为30:70的油包水乳液,然后进行NaOH溶液处理。水相由甲醇,四异丙醇钛,二乙醇胺,SiO2纳米颗粒和H2O组成,而油相由煤油,Span 80和Span 60组成。所得的微球具有111.7 m2·g-1的高比表面积。在模拟体液中,在8天内在微球表面形成了具有网状表面结构的磷灰石。微球的良好磷灰石形成能力归因于它们的多孔结构和TiO2的负Zeta电位。罗丹明B(一种亲水性药物的模型)的释放在浸泡的最初6小时内迅速释放,但此后进行扩散控制。在最初的6小时内爆发释放对于临床应用是有问题的。尽管如此,目前的结果强调了多孔TiO2微球作为能够形成磷灰石的释药水泥填料的潜力。

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