Literature DB >> 1614963

Simultaneous in vitro measurement of intestinal tissue permeability and transepithelial electrical resistance (TEER) using Sweetana-Grass diffusion cells.

S C Sutton1, A E Forbes, R Cargill, J H Hochman, E L LeCluyse.   

Abstract

A simple modification of the commercially available Sweetana-Grass (S-G) side-by-side diffusion cells, allowing the simultaneous measurement of tissue permeability and transepithelial electrical resistance (TEER), has been described and validated for rat excised, muscle-free intestinal tissue. The TEER-lowering effects of a series of acylcarnitines were shown to be correlated with previously reported in vitro (i.e., membrane perturbation) and in vivo (i.e., absorption enhancement) activity. The TEER-lowering effect of palmitoyl carnitine chloride (PCC) was also shown to be reversible. The effects of PCC on TEER and the permeability of poorly absorbed compounds (cefoxitin and lucifer yellow) were simultaneously determined. Compared to controls (mannitol-treated), PCC immediately produced a rapid drop in colon TEER. By 5 min post-PCC addition, colon TEER was 50% of control; by 10 min post-PCC addition, colon TEER was 17% of control. After a lag of about 5-10 min post-PCC addition, the cefoxitin or lucifer yellow permeability coefficient increased more than 20-fold. The modified S-G cells provide a simple and reproducible method whereby flux and TEER can be simultaneously determined, providing a valuable link between the effect of absorption enhancers on TEER measurements and the increased permeability of poorly absorbed compounds.

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Year:  1992        PMID: 1614963     DOI: 10.1023/a:1015878516157

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  7 in total

1.  Active transport of sodium as the source of electric current in the short-circuited isolated frog skin.

Authors:  H H USSING; K ZERAHN
Journal:  Acta Physiol Scand       Date:  1951-08-25

2.  In vitro measurement of gastrointestinal tissue permeability using a new diffusion cell.

Authors:  G M Grass; S A Sweetana
Journal:  Pharm Res       Date:  1988-06       Impact factor: 4.200

3.  Enhanced bioavailability of cefoxitin using palmitoyl L-carnitine. I. Enhancer activity in different intestinal regions.

Authors:  S C Sutton; E L LeCluyse; L Cammack; J A Fix
Journal:  Pharm Res       Date:  1992-02       Impact factor: 4.200

4.  Relationship between drug absorption enhancing activity and membrane perturbing effects of acylcarnitines.

Authors:  E L LeCluyse; L E Appel; S C Sutton
Journal:  Pharm Res       Date:  1991-01       Impact factor: 4.200

5.  Characterization of enhanced intestinal permeability; electrophysiological study on the effects of diclofenac and ethylenediaminetetraacetic acid.

Authors:  S Yamashita; H Saitoh; K Nakanishi; M Masada; T Nadai; T Kimura
Journal:  J Pharm Pharmacol       Date:  1985-07       Impact factor: 3.765

6.  Acylcarnitines: drug absorption-enhancing agents in the gastrointestinal tract.

Authors:  J A Fix; K Engle; P A Porter; P S Leppert; S J Selk; C R Gardner; J Alexander
Journal:  Am J Physiol       Date:  1986-09

7.  Cellular mechanism of intestinal permeability alterations produced by chelation depletion.

Authors:  M M Cassidy; C S Tidball
Journal:  J Cell Biol       Date:  1967-03       Impact factor: 10.539

  7 in total
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2.  Effects of acylcarnitines on efflux transporting system in Caco-2 cell monolayers.

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5.  Absorption-enhancing effects of sodium caprate and palmitoyl carnitine in rat and human colons.

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  5 in total

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