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Positively Charged Gelatin Microspheres as Gastric Mucoadhesive Drug Delivery System for Eradication of H. pylori.

Authors :
Wang, Jian
Tauchi, Yoshihiko
Deguchi, Yoshiharu
Morimoto, Kazuhiro
Tabata, Yasuhiko
Ikada, Yashito
Source :
Drug Delivery; Oct2000, Vol. 7 Issue 4, p237-243, 7p, 1 Chart, 6 Graphs
Publication Year :
2000

Abstract

Gastric mucoadhesive drug delivery systems are very promising for eradication of Helicobacter pylori (H. pylori), a spiral bacterium that resides in the gastric mucus layer and at the mucus- epithelial cell interface. New positively charged biodegradable microspheres were prepared using aminated gelatin by surfactantfree emulsification in olive oil, followed by a cross-linking reaction with glutaraldehyde. The amino group contents of the modified gelatin and the microspheres were determined using a 2,4,6-trinitrobenzenesulfonic acid method. With the increase of glutaraldehyde concentration, the amino group content of the microspheres decreased accordingly. The influence of glutaraldehyde concentration, cross-linking reaction time, drug-loading patterns, and type of release media on the in vitro release characteristics of amoxicillin from the microspheres was investigated. Amoxicillin release rate from the modified gelatin microspheres was significantly reduced compared with that from gelatin microspheres. Furthermore, the release was decreased with the increase of glutaraldehyde concentration and/or cross-linking time. On the other hand, a faster release was observed in a lower pH release medium and/or using a lower pH solution for amoxicillin loading. The gastric mucoadhesive properties of the microspheres were evaluated using RITC-labeled microspheres in an isolated rat stomach. The gastric mucoadhesion of the modified gelatin microspheres was markedly improved compared with that of gelatin microspheres. The modified gelatin microsphere proves to be a possible candidate delivery system for the effective eradication of H. pylori. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10717544
Volume :
7
Issue :
4
Database :
Complementary Index
Journal :
Drug Delivery
Publication Type :
Academic Journal
Accession number :
4011592
Full Text :
https://doi.org/10.1080/107175400455173