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PEG-Hydrogel Coated Silica Aerogels: A Novel Drug Delivery System

机译:PEG-Hydrogel涂层二氧化硅气凝胶:一种新型药物递送系统

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A novel composite of silica aerogel-poly(ethylene glycol) PEG hydrogel was synthesized and its potential as a drug delivery system was investigated. The composite was synthesized by encapsulation of hydrophobic aerogels within PEG hydrogel via photoinitiated polymerization. Disks of aerogels were synthesized by the two step sol-gel method using tetraethylortosilicate (TEOS) as the silica precursor. After aging in ethanol, the alcogels were loaded with eosin-Y photoinitiator. The surface of eosin functionalized silica aerogels was then rendered hydrophobic using hexamethyldisilazane (HMDS) as the surface modification agent, and supercritical carbon dioxide (scCO_2) as the solvent. Hydrophobicity of aerogel was tuned by changing HMDS amount dissolved in ScCO_2 phase which resulted in the change of the contact angle between 0 and 128°. Hydrophobic or hydrophilic aerogels were then dipped into a PEG diacrylate prepolymer solution, and photopolymerization was carried out using visible light (514 nm). BET surface area and pore size distribution measurements showed that both hydrogel encapsulation and eosin-Y loading did not affect the pore structure of the aerogel. The potential of this composite as a drug delivery system was tested by Ketoprofen as a model drug. The results demonstrate that both drug loading capacity and drug release profiles could be tuned by changing the hydrophobicity of aerogels, and that drug loading capacity increases with decreased aerogel hydrophobicity while slower release rates are achieved with increased hydrophobicity from eosin functionalized aerogels. The effect of PEG concentration (0, 15 %, and 30 % w/w) in the prepolymer solution of the hydrogel coating on drug release rate from hydrophilic aerogel was also investigated. It was seen that as the PEG concentration increased, the drug release was retarded. The experimental results showed that drug release can be controlled with this novel aerogel-hydrogel composite system via changing hydrophobicity of the aerogel, and the concentration of the PEG in the hydrogel coating.
机译:二氧化硅气凝胶 - 聚(乙二醇)PEG水凝胶的合成及其作为药物递送系统的潜在的新的复合的影响。该复合物通过经由光引发聚合的PEG水凝胶内的疏水气凝胶的封装合成。气凝胶圆盘由作为所述二氧化硅前体使用tetraethylortosilicate(TEOS)两步溶胶 - 凝胶法合成。在乙醇中老化后,将醇凝胶装载有曙红-Y光引发剂。然后曙红官能化的二氧化硅气凝胶的表面是使用六甲基二硅氮烷(HMDS)作为表面改性剂赋予疏水性,和超临界二氧化碳(scCO_2)作为溶剂。气凝胶的疏水性,通过改变HMDS量溶解在ScCO_2相,其结果为0和128之间的接触角°的变化进行调整。然后疏水或亲水气凝胶浸入一个PEG二丙烯酸酯的预聚物溶液中,光聚合是使用可见光(514纳米)。 BET表面积和孔径分布的测量表明,两种水凝胶封装和曙红-Y负荷不影响该气凝胶的孔隙结构。此复合物作为药物递送系统的潜力被测试酮洛芬作为模型药物。结果表明,这两种载药能力和药物释放曲线可以通过改变气凝胶的疏水性被调谐,并而较慢的释放速率与增加的疏水性伊红官能气凝胶实现与载药量增加而减少气凝胶的疏水性。在从亲水气凝胶的药物释放速率,水凝胶涂层的预聚物溶液PEG浓度(0,15%,和30%重量/重量)的效果也进行了研究。可看出,随着PEG浓度增加,药物释放是智障。实验结果表明,药物释放可以通过改变气凝胶的疏水性这种新颖的气凝胶的水凝胶复合物系统,和PEG的水凝胶涂层的浓度来控制。

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