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Vol. 302, Issue 2, 532-538, August 2002
Department of Pharmacy, Kyoto University Hospital, Faculty of
Medicine, Kyoto University, Kyoto, Japan
Ulcerative colitis is a disease more commonly seen in nonsmokers.
Because nicotine was postulated to be a beneficial component of tobacco
smoke for ulcerative colitis, various formulations of nicotine have
been developed to improve the local bioavailability within the
gastrointestinal tissue. In the present study, to characterize the
disposition of nicotine in the intestines, we investigated intestinal
nicotine transport using Caco-2 cells. Nicotine was predominantly
transported across Caco-2 cell monolayers in a unidirectional mode,
corresponding to intestinal secretion, by pH-dependent specific transport systems. The specific uptake systems appear to be distinct from organic cation transporters and the transport system for tertiary
amines, in terms of its substrate specificity and the pattern of the
interaction. These transport systems could play a role in the
intestinal accumulation of nicotine from plasma and could also be
responsible for the topical delivery of nicotine for ulcerative colitis
therapy. These findings could provide useful information for the design
of effective nicotine delivery.
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