Interdisciplinary Program in Bioengineering, College of Engineering, Seoul National University, Seoul 152-742, Republic of Korea.
Acta Biomater. 2014 Jan;10(1):77-86. doi: 10.1016/j.actbio.2013.08.026. Epub 2013 Aug 23.
We describe nanostructured microparticles (NMs) containing a mucoadhesive polymer for enhanced preocular retention and consider them as potential carriers of drugs to the eye. These NMs are each composed of entangled nanofibers to give an enlarged specific surface area, and thus can better adhere to the preocular mucus surface. This physical design allows the microparticles still to be composed mainly of a wall material, poly(lactic-co-glycolic acid), as required for controlled drug delivery, while the effects of an additive, mucoadhesive material, polyethylene glycol, can be synergistically improved via the nanostructured morphology. Thus, when formulated in a dry tablet dosage form, the NMs in this work show more than a 10-fold increase in preocular retention in vivo compared to conventional spherical microparticles. Therefore, we conclude that these mucoadhesive NMs can reside on the preocular surface for a prolonged period, and thus appear to be a promising system for topical drug delivery to the eye.
我们描述了含有一种粘液附着聚合物的纳米结构微颗粒(NMs),以增强眼前滞留,并将其视为药物输送到眼睛的潜在载体。这些 NMs 由缠结的纳米纤维组成,以增加比表面积,从而更好地附着在眼前粘液表面上。这种物理设计允许微颗粒仍然主要由壁材料,即聚(乳酸-共-乙醇酸)组成,这是控制药物释放所必需的,而添加剂,即粘液附着材料,聚乙二醇的作用可以通过纳米结构形态协同增强。因此,当以干燥片剂的形式配制时,与传统的球形微颗粒相比,本工作中的 NMs 在体内的眼前滞留时间增加了 10 倍以上。因此,我们得出结论,这些粘液附着的 NMs 可以在眼前表面上长时间停留,因此似乎是一种有前途的眼部局部药物递送系统。