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Antimicrobial Agents and Chemotherapy, November 2004, p. 4422-4426, Vol. 48, No. 11
0066-4804/04/$08.00+0 DOI: 10.1128/AAC.48.11.4422-4426.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Services de Pharmacologie et de Parasitologie, CHU du Kremlin-Bicêtre, Le Kremlin-Bicêtre, France,1 Unité d'Épidémiologie, Centre Muraz, Bobo Dioulasso, Burkina Faso2
Received 18 February 2004/ Returned for modification 24 May 2004/ Accepted 26 July 2004
The pharmacokinetics of increasing doses of an intrarectal Cinchona alkaloid combination containing 96.1% quinine, 2.5% quinidine, 0.68% cinchonine, and 0.67% cinchonidine (Quinimax) was compared to that of parenteral regimens in 60 children with moderate malaria. Quinine exhibited a nonlinear pharmacokinetics, suggesting a saturation of rectal resorption. When early rejections appeared, blood quinine concentrations decreased by 30 to 50% and were restored by an immediate half-dose administration of the drug. Rectal administration of doses of 16 or 20 mg/kg of body weight led to concentration-time profiles in blood similar to those of parenteral regimens and could be an early treatment of childhood malaria.
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