Bioavailability of 5-aminosalicylic acid from slow release 5-aminosalicylic acid drug and sulfasalazine in normal children |
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Authors: | Dr. Lisbet A. Christensen MD Jan Fallingborg MD Bent A. Jacobsen MD Kirsten Abildgaard MD Henrik H. Rasmussen MD Sten N. Rasmussen MD Steen H. Hansen DSc |
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Affiliation: | 1. Department of Medical Gastroenterology, Aalborg Hospital, DK 9000, Aalborg, Denmark 2. Department of Surgical Gastroenterology, Aalborg Hospital, Denmark 3. Department of Organic Chemistry, Royal Danish School of Pharmacy, Copenhagen, Denmark
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Abstract: | The bioavailability of a controlled release 5-aminosalicylic acid preparation (Pentasa) was investigated in nine healthy children after a medication period of six days (1000 mg/day) and compared with sulfasalazine (Salazopyrin) (2000 mg/day). The local bioavailability in the distal gut lumen, reflected by the 5-aminosalicylic acid concentration in the fecal water, showed comparable values after Pentasa (4.44 mmol/liter) and Salazopyrin (6.25 mmol/liter). The concentration ofN-acetyl-5-ASA was significantly higher after Pentasa, reflecting the more proximal release of 5-aminosalicylic acid compared with Salazopyrin. No relation was found between the 5-aminosalicylic acid fecal water concentration and the 5-aminosalicylic acid dose per kilogram of body weight. The urinary excretion of 5-aminosalicylic acid andN-acetyl-5-aminosalicylic acid was higher after Pentasa than after Salazopyrin (32% vs 25%). Dose interval plasma concentration curves showed low values after both preparations. Based on the concept that the fecal water concentration is decisive for the efficacy of 5-aminosalicylic acid in distal inflammatory bowel disease, Pentasa treatment offers a relevant alternative in cases of Salazopyrin intolerance or allergy in children. The higher systemic bioavailability from Pentasa warrants monitoring of the renal function. |
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