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Absorption enhancing effects of chitosan oligomers on the intestinal absorption of low molecular weight heparin in rats

  • Xi'an Jiaotong University
  • Kyoto Pharmaceutical University

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Absorption enhancing effects of chitosan oligomers with different type and varying concentration on the intestinal absorption of low molecular weight heparin (LMWH) were examined by an in situ closed loop method in different intestinal sections of rats. Chitosan hexamer with the optimal concentration of 0.5% (w/v) showed the highest absorption enhancing ability both in the small intestine and large intestine. The membrane toxicities of chitosan oligomers were evaluated by morphological observation and determining the biological markers including amount of protein and activity of lactate dehydrogenase (LDH) released from intestinal epithelium cells. There was no obvious change both in levels of protein and LDH and morphology in the intestinal membrane between control and various chitosan oligomers groups, suggesting that chitosan oligomers did not induce any significant membrane damage to the intestinal epithelium. In addition, zeta potentials became less negative and amount of free LMWH gradually decreased when various chitosan oligomers were added to LMWH solution, revealing that electrostatic interaction between positively charged chitosan oligomers and negative LMWH was included in the absorption enhancing mechanism of chitosan oligomers. In conclusion, chitosan oligomers, especially chitosan hexamer, are safe and efficient absorption enhancers and can be used promisingly to improve oral absorption of LMWH.

Original languageEnglish
Pages (from-to)156-162
Number of pages7
JournalInternational Journal of Pharmaceutics
Volume466
Issue number1-2
DOIs
StatePublished - 15 May 2014

Keywords

  • Absorption enhancer
  • Chitosan oligomers
  • Electrostatic interaction
  • Intestinal absorption
  • Low molecular weight heparin (LMWH)
  • Membrane toxicity

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