Preparation and characterization of a novel pH-sensitive coated microsphere for duodenum-specific drug delivery

被引:7
|
作者
Zhou, Dan [1 ]
Zhu, Xi [1 ]
Wang, Yang [2 ]
Jin, Yun [1 ]
Xu, Xuefan [1 ]
Fan, Tingting [1 ]
Liu, Yan [1 ]
Zhang, Zhirong [1 ]
Huang, Yuan [1 ]
机构
[1] Sichuan Univ, Key Lab Drug Targeting & Drug Delivery Syst, Minist Educ, W China Sch Pharm, Chengdu 610041, Peoples R China
[2] Chongqing Med Univ, Teaching & Res Unit Hygien Toxicol, Sch Publ Hlth, Chongqing 400016, Peoples R China
关键词
HPMCAM-coated mucoadhesive microspheres; Furazolidone-loaded mucoadhesive microspheres; Duodenum-specific; pH-Sensitive; Morphological changes; Drug release; PREDNISOLONE CONJUGATE MICROSPHERES; HELICOBACTER-PYLORI THERAPY; IN-VIVO EVALUATION; MUCOADHESIVE MICROSPHERES; CHITOSAN MICROSPHERES; DISSOLUTION PROFILES; CONTROLLED-RELEASE; VITRO EVALUATION; MICROPARTICLES; AMOXICILLIN;
D O I
10.1007/s12272-012-0509-9
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The aim of this study is to develop a duodenum-specific drug delivery system on the basis of a pH-sensitive coating and a mucoadhesive inner core for eradication of Helicobacter pylori (H. pylori) in the ulcer duodenum. Hydroxypropyl methylcellulose acetate maleate (HPMCAM) was used as the pH-sensitive material, which dissolves around pH 3.0. The mucoadhesive microspheres loaded with furazolidone (FZD-ad-MS) were prepared by the emulsification-solvent evaporation method using Carbopol 971NP as the mucoadhesive polymer. The prepared pH-sensitive coated mucoadhesive microspheres (AM-coated-MS) were characterized in regards to particle size, drug loading efficiency, morphological change, drug stability, drug release and in vitro anti-H. pylori activity. The particle size was 160.97 +/- 47.24 mu m and 336.44 +/- 129.34 mu m, and the drug content was 42.33 +/- 3.43% and 10.96 +/- 1.29% for FZD-ad-MS and AM-coated-MS, respectively. The morphological changes in different pH media were characterized by scanning electron microscopy (SEM). HPMCAM coating improved the stability of the FZD-ad-MS and these particles were expected to remain intact until their arrival in the duodenum. The drug release was extremely suppressed at pH 1.2 for AM-coated-MS, but increased at pH 4.0 after regeneration of FZD-ad-MS. In addition, FZD-ad-MS exhibited excellent anti-H. pylori activity in vitro. Thus, the HPMCAM-coated microspheres developed in this study hold great promise for use as a duodenum-specific drug delivery system for H. pylori clearance.
引用
收藏
页码:839 / 850
页数:12
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