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用于十二指肠靶向给药系统的 pH 敏感型和黏膜黏附型微球。

pH-sensitive and mucoadhesive microspheres for duodenum-specific drug delivery system.

机构信息

Key Laboratory of Drug Targeting and Drug Delivery, Ministry of Education, West China School of Pharmacy, Sichuan University, Chengdu, PR China.

出版信息

Drug Dev Ind Pharm. 2011 Jul;37(7):868-74. doi: 10.3109/03639045.2010.546801. Epub 2011 Jan 14.

Abstract

Particulate systems that could deliver drug specifically to duodenum have not yet been reported. The aim of this study was to develop a novel duodenum-specific drug delivery system based on thiolated chitosan and hydroxypropyl methylcellulose acetate maleate (HPMCAM) for the duodenal ulcer application. Berberine hydrochloride was used as model drug. Thiolated chitosan was synthesized and further used for the preparation of mucoadhesive microspheres. HPMCAM, which is insoluble below pH 3.0 was synthesized and used for the coating of thiolated chitosan microspheres (TCM). The resulting thiolated chitosan immobilized on chitosan was 268.21 ± 18 μmol/g. In vitro mucoadhesion study showed that the mucoadhesion property of TCM was better than that of chitosan microspheres. Morphological observation showed that the HPMCAM coating would maintain its integrity in simulated gastric fluid (SGF) for 2 h and dissolved quickly in simulated pathological duodenal fluid (SPDF; pH 3.3). In vitro drug release studies showed that only 4.75% of the drug was released in SGF for 2 h, while nearly 90% of the drug was released within 6 h after transferring into SPDF.

摘要

尚未有报道称,有能够将药物专门递送至十二指肠的颗粒系统。本研究旨在开发一种基于巯基化壳聚糖和羟丙基甲基纤维素醋酸琥珀酸酯(HPMCAM)的新型十二指肠特异性药物传递系统,用于十二指肠溃疡的治疗。盐酸小檗碱被用作模型药物。合成了巯基化壳聚糖,并进一步用于制备粘弹性微球。HPMCAM 在 pH 值低于 3.0 时不溶解,被合成并用于包裹巯基化壳聚糖微球(TCM)。固定在壳聚糖上的巯基化壳聚糖的量为 268.21±18 μmol/g。体外粘膜黏附研究表明,TCM 的粘膜黏附性能优于壳聚糖微球。形态观察表明,HPMCAM 涂层在模拟胃液(SGF)中可保持完整 2 小时,在模拟病理十二指肠液(SPDF;pH 3.3)中迅速溶解。体外药物释放研究表明,在 SGF 中 2 小时内仅释放了 4.75%的药物,而在转移到 SPDF 后 6 小时内几乎释放了 90%的药物。

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