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Sol–gel one-pot synthesis in soft conditions of mesoporous silica materials ready for drug delivery system

机译:溶胶-凝胶一锅法合成,在软条件下可用于药物输送系统的介孔二氧化硅材料

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摘要

The present work reveals a new and simple strategy, a one-step sol–gel procedure, to encapsulate a low water-soluble drug in silica mesostructured microparticles and to improve its release in physiological media. The synthesis of these new materials is based on the efficient solubilisation of a poorly water-soluble drug in surfactant micelles (Tween 80, a pharmaceutical excipient) which act as template for the silica network. A strict control of the sol–gel process and the parameters procedure in soft conditions (concentration, pH, temperature) was applied to reach the solubilisation limit of the drug in the micellar solution so as to optimise its encapsulation. Even if this one-pot procedure could appear limited by the low drug loading, it could provide an interesting alternative for the formulation of many recent highly active but very poorly soluble drugs.
机译:本工作揭示了一种新的简单策略,即一步法溶胶-凝胶法,可以将低水溶性药物包裹在二氧化硅介孔结构的微粒中,并改善其在生理介质中的释放。这些新材料的合成是基于水溶性差的药物在表面活性剂胶束(吐温80,一种药物赋形剂)中的有效增溶作用,该胶束充当二氧化硅网络的模板。在软条件下(浓度,pH,温度)严格控制溶胶-凝胶过程和参数程序,以达到药物在胶束溶液中的溶解极限,从而优化其封装。即使这种一锅法程序似乎受到低载药量的限制,它仍可以为配制许多最近的高活性但难溶性极高的药物提供有趣的替代方法。

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