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Polymer film formulations for the preparation of enteric pharmaceutical capsules.

机译:用于制备肠溶性药物胶囊的聚合物薄膜制剂。

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Objectives Standard pharmaceutical capsules are designed to dissolve in the acidic environment of the stomach releasing the encapsulated contents for absorption. When release is required further along the gastrointestinal tract capsules can be coated with acid insoluble polymers to enable passage through the stomach and dissolution in the intestine. This paper describes formulations that have the potential to be used to produce two-piece hard capsules for post-gastric delivery without the requirement of an exterior coat. Methods The formulation uses three polysaccharides: sodium alginate, hypromellose and gellan gum to provide acid insolubility and the ability to form capsules using standard industrial equipment. Key findings The rheological profile, on cooling, of the base material, water content and thickness of the films were shown to be comparable with those of commercial capsules. The capsules remained intact for 2 h in 100 mm HCl at pH 1.2, and within 5 min of being removed from the acid and submerged in phosphate-buffered saline at pH 6.8 were ruptured. Conclusions Selected formulations from this study have potential for use as delayed release capsules.
机译:目的标准药物胶囊设计用于在胃的酸性环境中溶解,释放出被吸收的胶囊化内容物。当需要沿着胃肠道进一步释放时,可以用不溶于酸的聚合物包被胶囊,以使其能够通过胃并在肠中溶解。本文介绍了可用于生产两件式硬胶囊的配方,无需胃外涂层即可用于胃后给药。方法该制剂使用三种多糖:海藻酸钠,羟丙甲纤维素和吉兰糖胶,以提供酸不溶性和使用标准工业设备形成胶囊的能力。主要发现冷却后,基础材料的流变特性,薄膜的水含量和厚度被证明与商业胶囊相当。胶囊在pH 1.2的100 mm HCl中保持完整2小时,并在从酸中取出并浸入pH 6.8的磷酸盐缓冲盐水中后5分钟内破裂。结论从这项研究中选择的制剂具有用作延迟释放胶囊的潜力。

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