Sumatriptan Absorption from Different Regions of the Human Gastrointestinal Tract |
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Authors: | Warner Patricia E. Brouwer Kirn L. R. Hussey Elizabeth K. Dukes George E. Donn Karl H. Davis Ian M. Powell J. Robert Heizer William D. |
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Affiliation: | (1) School of Pharmacy, University of North Carolina, Chapel Hill, North Carolina;(2) Department of Clinical Pharmacology, Glaxo Inc. Research Institute, Research Triangle Park, North Carolina, 27709;(3) School of Medicine, University of North Carolina, Chapel Hill, North Carolina, 27599;(4) Present address: College of Pharmacy, Xavier University of Louisiana, USA;(5) Present address: School of Pharmacy, University of Maryland, USA;(6) Division of Pharmaceutics, School of Pharmacy, The University of North Carolina at Chapel Hill, CB #7360, Beard Hall, Room 23, Chapel Hill, North Carolina, 27599-7360 |
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Abstract: | Sumatriptan exhibits low oral bioavailability partly due to presystemic metabolism, which may vary with regional differences in metabolic activity throughout the gastrointestinal tract. This study evaluated sumatriptan absorption in humans after administration orally and by oroenteric tube into the jejunum and cecum. Because the site of cecal administration varied, pharmacokinetic parameters for sumatriptan and its major metabolite were compared statistically only after oral and jejunal administration. One-half of the oral dose was recovered in the urine as parent (3%) and metabolite (46%). Sumatriptan was absorbed throughout the gastrointestinal tract; absorption was similar after oral and jejunal administration, and less after cecal administration. The metabolite AUC and the AUC ratio (metabolite/parent) were significantly lower after jejunal compared to oral administration; the AUC ratio was two-fold lower after cecal administration. Results suggest that presystemic metabolism of sumatriptan varies throughout the gastrointestinal tract and/or regional differences exist in the absorption of metabolite formed within the gastrointestinal tract. |
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Keywords: | sumatriptan gastrointestinal tract absorption metabolism pharmacokinetics |
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