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pH-sensitive mesalazine carrier for colon-targeted drug delivery: A two-fold composition of mesalazine with a clay and alginate

Authors
Hong, Hye-JinKim, JiwoongSuh, Yong JaeKim, DaeyoungRoh, Ki-MinKang, Ilmo
Issue Date
Nov-2017
Publisher
SPRINGER
Keywords
targeted drug delivery; side effect; smectite; alginate hydrogel
Citation
MACROMOLECULAR RESEARCH, v.25, no.11, pp.1145 - 1152
Journal Title
MACROMOLECULAR RESEARCH
Volume
25
Number
11
Start Page
1145
End Page
1152
URI
http://scholarworks.bwise.kr/ssu/handle/2018.sw.ssu/39273
DOI
10.1007/s13233-017-5150-5
ISSN
1598-5032
Abstract
The release of mesalazine, an anti-inflammatory drug for Crohn's disease, should be deferred while delivering along the gastrointestinal tract to maximize drug absorption in the colon. To that end, we intercalated mesalazine into a clay mineral, montmorillonite (MMT), and we encapsulated the resulting composite inside a pHsensitive polymer, an alginate hydrogel bead. Once intercalated between the microscopic MMT layers, the mesalazine is prevented from dissolution during encapsulation into the alginate beads. As the resulting mesalazine-clay-alginate (MCA) bead is covered with a protective alginate layer, the mesalazine does not dissolve in acidic gastric conditions. In in vitro release tests, the MCA beads exhibited less than 5% mesalazine release in gastric solution, while similar to 20% was released over 7 h in the intestinal condition. Our results demonstrate that the MCA bead is a highly effective, biocompatible means of mesalazine delivery to the colon.
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