Shimono Norihito, Ueda Masumi, Nakamura Yasuhiko
Formulation Group, Pharmaceutical Research Laboratories, Dainippon Pharmaceutical Co., Ltd., Osaka, Japan.
Chem Pharm Bull (Tokyo). 2002 Sep;50(9):1169-75. doi: 10.1248/cpb.50.1169.
Pellets containing active ingredients were coated with water-insoluble powders, i.e. hydrogenated caster oil (Lubliwax (WAX)) and magnesium stearate (Mg-St). The influences of the structural difference of the sustained release layer and curing conditions on the drug release rate were investigated. Sodium valproate (VP-Na) was used as a highly water-soluble model drug. Drug release profiles were influenced by the combination of the WAX layer and the Mg-St layer. Even if the formula of sustained release layers were the same, drug release rate could be affected by the structural difference of the controlled release layer. The Mg-St layer was more effective in prolonging drug release than the WAX layer. Compared with single and double layer types, the triple layer (sandwich) type was most effective in obtaining a long sustained drug release. Heat-treatment retarded drug release mainly by increasing the density of the sustained release layer of the WAX. The Mg-St was effective in protecting the agglomeration between particles during heat-treatment. Optimal heat-treatment conditions were found to exist. Scanning electron microscopy (SEM) analysis indicated that heat-treatment caused the WAX to melt, formed a film-like structure and made the release layer dense. Furthermore, heat-treatment changed the release pattern of VP-Na from sustained release pellets with a multi-layer of powder, leading to zero-order release.
含有活性成分的小丸用不溶于水的粉末包衣,即氢化蓖麻油(Lubliwax(WAX))和硬脂酸镁(Mg-St)。研究了缓释层的结构差异和固化条件对药物释放速率的影响。丙戊酸钠(VP-Na)用作高水溶性模型药物。药物释放曲线受WAX层和Mg-St层组合的影响。即使缓释层的配方相同,控释层的结构差异也可能影响药物释放速率。Mg-St层在延长药物释放方面比WAX层更有效。与单层和双层类型相比,三层(夹心)类型在实现长时间持续药物释放方面最有效。热处理主要通过增加WAX缓释层的密度来延缓药物释放。Mg-St在热处理过程中对保护颗粒间的团聚有效。发现存在最佳热处理条件。扫描电子显微镜(SEM)分析表明,热处理使WAX熔化,形成薄膜状结构并使释放层致密。此外,热处理改变了多层粉末缓释小丸中VP-Na的释放模式,导致零级释放。