pH-Dependent and Carrier-mediated Transport of Salicylic Acid Across Caco-2 Cells

Author:

Takanaga Hitomi1,Tamai Ikumi1,Tsuji Akira1

Affiliation:

1. Department of Pharmaceutics, Faculty of Pharmaceutical Sciences, Kanazawa University, 13–1 Takara-machi, Kanazawa 920, Japan

Abstract

Abstract The transport of monocarboxylic acid drugs such as salicylic acid was examined in the human colon adenocarcinoma cell line, Caco-2 cells that possess intestinal epithelia-like properties. [14C]Salicylic acid transport was pH-dependent and appeared to follow the pH-partition hypothesis. However, 10 Mm unlabelled salicylic acid significantly reduced the permeability coefficient of [14C]salicylic acid. Kinetic analysis of the concentration dependence of the permeation rate of salicylic acid across Caco-2 cells showed both saturable (K1 = 5·28 ± 0·72 Mm Jmax = 36·6 ± 3·54 nmol min−1 (mg protein)−1) and non-saturable (kd = 0·37 ± 0·08 μL min−1 (mg protein)−1) processes. The permeation rate of [14C]salicylic acid was competitively inhibited by both acetic acid and benzoic acid, which were demonstrated in our previous studies to be transported in the carrier-mediated-transport mechanism which is responsible for monocarboxylic acids. Furthermore, certain monocarboxylic acids significantly inhibited [14C]salicylic acid transport, whereas salicylamide and dicarboxylic acids such as succinic acid did not. From these results, it was concluded that the transcellular transport of [14C]salicylic acid across Caco-2 cells is by the pH-dependent and carrier-mediated transport mechanism specific for monocarboxylic acids.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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