| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 598975 | Colloids and Surfaces B: Biointerfaces | 2016 | 10 Pages |
•Mucoadhesive microparculates were prepared for colon target dual drug delivery.•In vitro and in vivo properties of microparticulates were evaluated in detail.•Microparculates has pH-sensitive release property and could release drug in colon.•This drug-delivery system show superior therapeutic efficiency for the colitis rats.
In this work, thiolated chitosan/alginate composite microparticulates (CMPs) coated by Eudragit S-100 were developed for colon-specific delivery of 5-aminosalicylic acid (5-ASA) and curcumin (CUR), and the use of it as a multi drug delivery system for the treatment of colitis. The physicochemical properties of the CMPs were evaluated. In vitro release was performed in gradually pH-changing medium simulating the conditions of different parts of GIT, and the results showed that the Eudragit S-100 coating has a pH-sensitive release property, which can avoid drug being released at a pH lower than 7. An everted sac method was used to evaluate the mucoadhesion of CMPs. Ex vivo mucoadhesive tests showed CMPs have excellent mucosa adhesion for the colonic mucosa of rats. In vivo treatment effect of enteric microparticulates systems was evaluated in colitis rats. The results showed superior therapeutic efficiency of this drug delivery system for the colitis rats induced by TNBS. Therefore, the enteric microparticulates systems combined the properties of pH dependent delivery, mucoadhesive, and control release, and could be an available tool for the treatment of human inflammatory bowel disease.
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