Suppr超能文献

硫酸沙丁胺醇粘膜粘附贴片的研制及其用于口腔单向药物传递的特性研究。

Development and characterization of mucoadhesive patches of salbutamol sulfate for unidirectional buccal drug delivery.

机构信息

Department of Pharmaceutical Technology, Anna University of Technology, Tiruchirapalli, Tiruchirapalli 620 024, India.

出版信息

Acta Pharm. 2011 Jun;61(2):157-70. doi: 10.2478/v10007-011-0011-9.

Abstract

Buccal patches of salbutamol sulfate were prepared using five different water soluble polymers in various proportions and combinations using PEG-400/PG as plasticizers. A 32 full factorial design was used to design the experiments for each polymer combination. Patches were laminated on one side with a water impermeable backing layer for unidirectional drug release. The thickness of medicated patches ranged between 0.2 and 0.4 mm and showed an increase in mass whenever PEG-400 was used as plasticizer. The surface pH of all patches approached neutral. Eight formulations which had shown high folding endurance (> 300) were selected for evaluation. Patches prepared with PEG-400 showed a high swelling index. The residence time of the tested patches ranged between 105 and 130 min. Formulations A10, A32, B10 and B32 fitted the Higuchi model best, whereas formulations A19 and B19 showed super case II transport drug release. Stability studies indicated that there was no change in the chemical and physical characteristics during the test period of 6 months.

摘要

采用不同比例和组合的 5 种水溶性聚合物,使用 PEG-400/PG 作为增塑剂,制备硫酸沙丁胺醇颊贴片。对于每种聚合物组合,均采用 32 全因子设计来设计实验。贴片的一侧用不透水的背衬层进行层压,以实现单向药物释放。含药贴片的厚度在 0.2 至 0.4 毫米之间,并且只要使用 PEG-400 作为增塑剂,其质量就会增加。所有贴片的表面 pH 值均接近中性。选择了 8 种具有高折叠耐力 (>300)的制剂进行评估。用 PEG-400 制备的贴片具有较高的溶胀指数。所测试的贴片的滞留时间在 105 至 130 分钟之间。制剂 A10、A32、B10 和 B32 最符合 Higuchi 模型,而制剂 A19 和 B19 则显示出超 II 型药物释放。稳定性研究表明,在 6 个月的测试期间,化学和物理特性没有变化。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验