首页> 外文期刊>Journal of pharmaceutical sciences. >Novel starch-based PVA thermoplastic capsules for hydrophilic lipid-based formulations
【24h】

Novel starch-based PVA thermoplastic capsules for hydrophilic lipid-based formulations

机译:用于亲水脂质基制剂的新型淀粉基PVA热塑性胶囊

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

For decades, gelatin has been used in the rotary die process as a shell-forming material of soft capsules because of its unique physicochemical properties. However, with respect to the encapsulation of comparatively hydrophilic lipid-based formulations, gelatin has one considerable drawback: Immediately after production, the capsule shell contains a large amount of water (up to 35%). There is the potential for water to migrate from the capsule shell into the formulation, which will lead to a decrease in drug solubility and, in turn, the potential for drug crystallization. The present study introduces a novel capsule material that was obtained from extrusion. The starch-based polyvinyl alcohol thermoplastic capsules (S-PVA-C) mainly comprised a blend of starch and PVA. Gelatin and the novel material were used to encapsulate a hydrophilic lipid-based system of fenofibrate. Considerable water migration was observed from the soft gelatin shell to the hydrophilic formulation during drying and drug crystallization resulted in soft gelatin capsules. In contrast, S-PVA-C displayed no substantial water exchange or drug crystallization upon storage. The thermoplastic capsule material further exhibited more surface roughness and higher resistance to mechanical deformation compared with gelatin. In conclusion, S-PVA-C provided a robust drug product following encapsulation of a rather hydrophilic lipid-based formulation.
机译:数十年来,明胶因其独特的物理化学特性而在旋转模头工艺中用作软胶囊的壳形成材料。然而,就相对亲水的基于脂质的制剂的封装而言,明胶具有一个相当大的缺点:在生产后,胶囊壳立即包含大量的水(高达35%)。水有可能从胶囊壳迁移到制剂中,这将导致药物溶解度降低,进而导致药物结晶。本研究介绍了一种通过挤压获得的新型胶囊材料。淀粉基聚乙烯醇热塑性胶囊(S-PVA-C)主要包含淀粉和PVA的混合物。明胶和新型材料用于封装非诺贝特的基于亲水脂质的系统。在干燥过程中观察到从软明胶壳到亲水制剂的大量水迁移,并且药物结晶导致软明胶胶囊。相反,S-PVA-C在储存时没有显示出大量的水交换或药物结晶。与明胶相比,热塑性胶囊材料还表现出更大的表面粗糙度和更高的抗机械变形性。总而言之,S-PVA-C封装了相当亲水的基于脂质的制剂后,提供了一种坚固的药物产品。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号