Laboratory for Pharmacotechnology and Biopharmacy, Katholieke Universiteit Leuven, Leuven 3000, Brabant, Belgium.
Center for Surface Chemistry and Catalysis, Katholieke Universiteit Leuven, Leuven 3001, Brabant, Belgium.
J Pharm Sci. 2011 Aug;100(8):3411-3420. doi: 10.1002/jps.22535. Epub 2011 Mar 8.
Ordered mesoporous silica (OMS) materials are considered a promising drug delivery system for the dissolution enhancement of poorly soluble compounds. The purpose of the present work was to determine structural and behavioral changes of compressed OMS material necessary for the development of an immediate-release oral-dosage formulation. Two types of OMS materials (SBA-15 and COK-12) were subjected to pressures both in and beyond the tabletting region and characterized by nitrogen physisorption, scanning and transmission electron microscopy, small-angle X-ray scattering, and differential scanning calorimetry. Itraconazole was used as the poorly soluble model drug and the release process with respect to pressure was determined in vitro. The resulting decreased drug release due to increased pressure was recovered by incorporating a plastically deforming material such as microcrystalline cellulose in combination with croscarmellose sodium. These findings further elucidate the understanding of their structural behavior for the advancement as a drug delivery carrier.
有序介孔硅(OMS)材料被认为是一种很有前途的药物输送系统,可提高难溶性化合物的溶解度。本工作的目的是确定压缩 OMS 材料的结构和行为变化,这些变化对于开发即时释放口服剂型是必要的。两种类型的 OMS 材料(SBA-15 和 COK-12)都承受了压片区域内外的压力,并通过氮气物理吸附、扫描和透射电子显微镜、小角 X 射线散射和差示扫描量热法进行了表征。伊曲康唑被用作难溶性模型药物,并且体外确定了药物释放与压力的关系。通过将塑性变形材料(如微晶纤维素)与交联羧甲基纤维素钠结合使用,可以恢复由于压力增加而导致的药物释放减少。这些发现进一步阐明了它们作为药物输送载体的结构行为的理解。