pH-Sensitive and mucoadhesive microspheres for duodenum-specific drug delivery system

被引:15
|
作者
Liu, Yue-Hua [1 ]
Zhu, Xi [1 ]
Zhou, Dan [1 ]
Jin, Yun [1 ]
Zhao, Chun-Yan [1 ]
Zhang, Zhi-Rong [1 ]
Huang, Yuan [1 ]
机构
[1] Sichuan Univ, W China Sch Pharm, Minist Educ, Key Lab Drug Targeting & Drug Delivery, Chengdu 610041, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Duodenum-specific; thiolated chitosan; mucoadhesion; pH-sensitive; enteric coating; CHITOSAN MICROSPHERES; HELICOBACTER-PYLORI; MICROPARTICLES; DERIVATIVES; POLYMERS; RELEASE; ULCER; ACID;
D O I
10.3109/03639045.2010.546801
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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 mu mu mol/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.</.
引用
收藏
页码:868 / 874
页数:7
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