Literature DB >> 15778050

Improvement of absorption enhancing effects of n-dodecyl-beta-D-maltopyranoside by its colon-specific delivery using chitosan capsules.

Gihan Fetih1, Sara Lindberg, Katsuhito Itoh, Naoki Okada, Takuya Fujita, Fawsia Habib, Per Artersson, Mohammed Attia, Akira Yamamoto.   

Abstract

In general, absorption enhancing effects of various absorption enhancers were greater in the large intestine than those in the small intestinal regions. Therefore, the effectiveness of absorption enhancers is expected to be remarkably observed, if these enhancers can be delivered to the large intestine with some poorly absorbable drugs after oral administration. In this study, therefore, we examined whether chitosan capsules were effective for the colon-specific delivery of a certain absorption enhancer and can improve the absorption enhancing action of the absorption enhancer after oral administration. 5(6)-Carboxyfluorescein (CF) was used as a model drug to investigate the site-dependent effectiveness of various absorption enhancers by an in situ closed loop method. Sodium glycocholate (NaGC), n-dodecyl-beta-d-maltopyranoside (LM), sodium salicylate (NaSal) and sodium caprate (NaCap) were used as models of absorption enhancers in this study. Overall, the absorption enhancing effects of these enhancers for intestinal absorption of CF were greater in the colon than those in the jejunum and the ileum. Especially, among these enhancers tested in this study, LM showed much greater absorption enhancing effect in the colon than in the jejunum and the ileum. Therefore, LM was selected as a model absorption enhancer to examine the effect of chitosan capsules on the absorption enhancing effect of LM. When CF and LM were orally administered to rats using chitosan capsules, the plasma concentration of CF was much higher than those in other dosage forms including solution and gelatin capsules. Therefore, chitosan capsules may be useful carriers for colon-specific delivery of LM, thereby increasing its absorption enhancing effect from the intestinal membranes.

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Year:  2005        PMID: 15778050     DOI: 10.1016/j.ijpharm.2004.12.017

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  3 in total

1.  Liposomes containing glycocholate as potential oral insulin delivery systems: preparation, in vitro characterization, and improved protection against enzymatic degradation.

Authors:  Mengmeng Niu; Yi Lu; Lars Hovgaard; Wei Wu
Journal:  Int J Nanomedicine       Date:  2011-06-08

Review 2.  Design of chitosan and its water soluble derivatives-based drug carriers with polyelectrolyte complexes.

Authors:  Qing-Xi Wu; Dong-Qiang Lin; Shan-Jing Yao
Journal:  Mar Drugs       Date:  2014-12-19       Impact factor: 5.118

Review 3.  Designing the new generation of intelligent biocompatible carriers for protein and peptide delivery.

Authors:  Angela M Wagner; Margaret P Gran; Nicholas A Peppas
Journal:  Acta Pharm Sin B       Date:  2018-03-02       Impact factor: 11.413

  3 in total

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