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基于酪蛋白的硅纳米复合药物输送系统的合成与生物响应。

Synthesis and biological response of casein-based silica nano-composite film for drug delivery system.

机构信息

College of Resources and Environment, Shaanxi University of Science and Technology, Xi'an 710021, Shaanxi Province, PR China.

College of Resources and Environment, Shaanxi University of Science and Technology, Xi'an 710021, Shaanxi Province, PR China.

出版信息

Colloids Surf B Biointerfaces. 2013 Nov 1;111:257-63. doi: 10.1016/j.colsurfb.2013.06.011. Epub 2013 Jun 17.

DOI:10.1016/j.colsurfb.2013.06.011
PMID:23831671
Abstract

Casein possesses many interesting properties that make it a good candidate for conventional and novel drug delivery systems. In this study, casein-based silica nano-composite was prepared via double in situ method, and the as-prepared latex particles were evaluated in terms of their morphology and size through transmission electron microscopy (TEM). The film morphology was investigated by scanning electron microscopy (SEM) and energy dispersive X-ray (EDX), and the mechanical property and response behavior of the films as a function of silica content were discussed. Ibuprofen was used as the model drug. The drug load and release properties were studied by solid-state nuclear magnetic resonance (solid-state NMR), Fourier transform infrared (FT-IR), SEM and in vitro test. The composite latex particle showed a stable core-shell structure, and the film exhibited a regular surface with even SiO2 distribution. The drug load efficiency of the composite films increased with adding silica because of the adsorption of the drugs on the silica. In an acidic release medium, the ibuprofen-loaded composite showed a slower drug release dependent on the silica content. These behaviors were most likely due to the reduced diffusion rate of the drug through the composite microsphere, which resulted from the interaction between the silica and the drug.

摘要

酪蛋白具有许多有趣的性质,使其成为传统和新型药物传递系统的良好候选物。在本研究中,通过双原位法制备了基于酪蛋白的硅纳米复合材料,并通过透射电子显微镜(TEM)评估了所制备的胶乳粒子的形态和尺寸。通过扫描电子显微镜(SEM)和能量色散 X 射线(EDX)研究了薄膜形态,并讨论了薄膜的机械性能和响应行为随二氧化硅含量的变化。布洛芬被用作模型药物。通过固态核磁共振(固态 NMR)、傅里叶变换红外(FT-IR)、SEM 和体外试验研究了药物的负载和释放性能。复合胶乳粒子呈现出稳定的核壳结构,薄膜具有均匀的 SiO2 分布的规则表面。由于药物在二氧化硅上的吸附,复合膜的药物负载效率随着添加二氧化硅而增加。在酸性释放介质中,负载布洛芬的复合膜显示出依赖于二氧化硅含量的较慢药物释放。这些行为可能归因于药物通过复合微球的扩散速率降低,这是由于二氧化硅与药物之间的相互作用所致。

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