Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
7791781 | Carbohydrate Polymers | 2014 | 7 Pages |
Abstract
The feeding regimen affects gut contents (mass and pH), more specifically in the stomach and lower intestine, and affects the rate of metabolism of diclofenac-β-cyclodextrin, but not that of sulfasalazine. The latter's degradation is much faster than that of diclofenac-β-cyclodextrin while the metabolism of both prodrugs is faster in colonic (versus caecal) contents. Fasting results in most rapid degradation of diclofenac-β-cyclodextrin, possibly due to lack of competition (absence of food) for microbial enzymatic activity.
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Authors
Amélia C.F. Vieira, Sudaxshina Murdan, Arménio C. Serra, Francisco J. Veiga, António M. d'A. Rocha Gonsalves, Abdul W. Basit,