Relationship between structure and permeability of dipeptide derivatives containing tryptophan and related compounds across human intestinal epithelial (Caco-2) cells.

Abstract:

:The permeability of dipeptide derivatives containing tryptophans and indole derivatives through Caco-2 cells was used as an in vitro intestinal absorption model in order to clarify structural factors which influence their intestinal epithelial permeation and metabolism. Most peptide derivatives were hydrolysed not only by the cytosolic enzymes in Caco-2 cells during permeation but also by enzymes released to the apical solution before cell permeation. The N-terminal blocked dipeptides were more resistant to hydrolases expressed in the Caco-2 cells and indole derivatives were not entirely degraded. Based on compound concentration dependency and comparison of permeability coefficients in apical-to-basolateral and basolateral-to-apical directions, the main absorption mechanism of compounds were determined. Compounds were then classified into three groups; (1) passively transported compounds, (2) actively transported compounds and (3) compounds excreted by P-glycoprotein.

journal_name

Bioorg Med Chem

authors

Ano R,Kimura Y,Urakami M,Shima M,Matsuno R,Ueno T,Akamatsu M

doi

10.1016/j.bmc.2003.10.001

subject

Has Abstract

pub_date

2004-01-02 00:00:00

pages

249-55

issue

1

eissn

0968-0896

issn

1464-3391

pii

S0968089603006734

journal_volume

12

pub_type

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