Li Zhuzhu, Li Qingxiu, Simon Sindee, Guven Necip, Borges Karin, Youan Bi-Botti C
Division of Pharmaceutical Sciences, University of Missouri-Kansas City, 5005 Rockhill Road, Kansas City, Missouri 64110-2499, USA.
J Pharm Sci. 2007 May;96(5):1018-30. doi: 10.1002/jps.20935.
This study evaluates the efficacy of the spray-drying technique in the bioengineering of phenytoin (PHT) containing poly(epsilon-caprolactone) (PCL) microcarrier intended for brain delivery for long-term treatment of epilepsy. Through orthogonally designed experiments, the optimal formulation and process variables for the preparation of PCL-microcarriers containing PHT were obtained. The produced microcarriers were characterized by coulter counter, scanning electron, scanning transmission electron microscopies, differential scanning calorimetry, powder X-ray diffraction, and in vitro release. The results showed that the produced microcarriers have a spherical structure, uniform size distribution, and a particle mean diameter of about 4.0 microm, which is suitable for brain delivery. The PHT was loaded as dispersed microcrystals within the PCL-microcarriers. From this system, PHT was released slowly into a buffer solution for approximately 14 days without any burst effect. These data suggested that PHT containing spray-dried PCL-microcarrier may be a promising drug delivery system for local brain delivery and long-term treatment of pharmacoresistant epilepsy.
本研究评估喷雾干燥技术在用于脑内递送以长期治疗癫痫的含苯妥英(PHT)聚(ε-己内酯)(PCL)微载体生物工程中的效果。通过正交设计实验,获得了制备含PHT的PCL微载体的最佳配方和工艺变量。所制备的微载体通过库尔特计数器、扫描电子显微镜、扫描透射电子显微镜、差示扫描量热法、粉末X射线衍射和体外释放进行表征。结果表明,所制备的微载体具有球形结构、尺寸分布均匀,颗粒平均直径约为4.0微米,适合脑内递送。PHT以分散的微晶形式负载在PCL微载体内。从该系统中,PHT缓慢释放到缓冲溶液中约14天,无任何突释效应。这些数据表明,含喷雾干燥PCL微载体的PHT可能是一种有前景的药物递送系统,用于局部脑内递送和耐药性癫痫的长期治疗。