Ahuja G, Pathak K
Rajiv Academy for Pharmacy, NH #2, P. O. Chhattikara, Mathura-281 001, India.
Indian J Pharm Sci. 2009 Nov;71(6):599-607. doi: 10.4103/0250-474X.59540.
Considerable research efforts have been directed in recent years towards the development of porous carriers as controlled drug delivery matrices because of possessing several features such as stable uniform porous structure, high surface area, tunable pore size and well-defined surface properties. Owing to wide range of useful properties porous carriers have been used in pharmaceuticals for many purposes including development of floating drug delivery systems, sustained drug delivery systems. Various types of pores like open, closed, transport and blind pores in the porous solid allow them to adsorb drugs and release them in a more reproducible and predictable manner. Pharmaceutically exploited porous adsorbents includes, silica (mesoporous), ethylene vinyl acetate (macroporous), polypropylene foam powder (microporous), titanium dioxide (nanoporous). When porous polymeric drug delivery system is placed in contact with appropriate dissolution medium, release of drug to medium must be preceded by the drug dissolution in the water filled pores or from surface and by diffusion through the water filled channels. The porous carriers are used to improve the oral bioavailability of poorly water soluble drugs, to increase the dissolution of relatively insoluble powders and conversion of crystalline state to amorphous state.
近年来,由于多孔载体具有稳定均匀的多孔结构、高比表面积、可调节的孔径和明确的表面性质等多种特性,大量的研究工作致力于将其开发为可控药物递送基质。由于具有广泛的有用特性,多孔载体已在制药领域用于多种目的,包括开发漂浮药物递送系统、缓释药物递送系统。多孔固体中的各种类型的孔,如开孔、闭孔、传输孔和盲孔,使它们能够以更可重复和可预测的方式吸附和释放药物。药学上利用的多孔吸附剂包括二氧化硅(介孔)、乙烯-醋酸乙烯酯(大孔)、聚丙烯泡沫粉末(微孔)、二氧化钛(纳米孔)。当多孔聚合物药物递送系统与合适的溶解介质接触时,药物向介质中的释放必须先于药物在充满水的孔中或从表面溶解,并通过充满水的通道扩散。多孔载体用于提高难溶性药物的口服生物利用度,增加相对不溶性粉末的溶解,并将结晶状态转化为无定形状态。