Kim Tae-Wan, Ji Chang-Won, Shim Sang-Young, Lee Beom-Jin
National Research Laboratory for Bioavailability Control, College of Pharmacy, Kangwon National University, Chuncheon 200-701, Korea.
Arch Pharm Res. 2007 Jan;30(1):124-30. doi: 10.1007/BF02977788.
A drug-containing polymeric dispersion was applied onto nonpareil sugar spheres (18/20 mesh) using a fluid-bed spray coater. Eudragit RS30D was selected as the polymeric coating material. Melatonin secreted by the pineal gland in a circadian rhythm was used as a model drug. The release behaviors of the coated sugar spheres were investigated in gastric fluid (pH 1.4) for 2 h, and then continuously in intestinal fluid (pH 7.4) for 14 h. The release rate of the coated sugar spheres decreased with increasing coating levels. The solvent (ethanol) in the coating dispersions significantly decreased the release of the drug due to the good dispersion of the low solubility melatonin in the polymeric films. The polymer (polyvinylpyrrolidone, PVP) and drug contents in the coating dispersions did not affect the release rate. Most of all, the release profiles were drastically changed according to the type and concentration of plasticizers used. The current coating methods that use drug-containing polymeric dispersions could be useful for simultaneous drug loadings and their modified release. The solubilization and controlled release of poorly water-soluble drugs can be achieved as both the solubilizers and drugs are present in the drug-containing polymeric dispersions.
使用流化床喷雾包衣机将含药聚合物分散体涂覆在无核糖球(18/20目)上。选择Eudragit RS30D作为聚合物包衣材料。以松果体按昼夜节律分泌的褪黑素作为模型药物。考察包衣糖球在胃液(pH 1.4)中2小时的释放行为,然后在肠液(pH 7.4)中连续考察14小时的释放行为。包衣糖球的释放速率随包衣水平的增加而降低。包衣分散体中的溶剂(乙醇)由于低溶解度的褪黑素在聚合物膜中的良好分散而显著降低了药物的释放。包衣分散体中的聚合物(聚乙烯吡咯烷酮,PVP)和药物含量不影响释放速率。最重要的是,释放曲线根据所用增塑剂的类型和浓度而发生显著变化。目前使用含药聚合物分散体的包衣方法对于同时进行药物负载及其缓释可能是有用的。由于增溶剂和药物都存在于含药聚合物分散体中,因此可以实现难溶性药物的增溶和控释。