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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/25599
Title: Absence of an interaction between artesunate and atovaquone-proguanil
Authors: M. Van Vugt
M. D. Edstein
S. Proux
K. Lay
M. Ooh
S. Looareesuwan
N. J. White
F. Nosten
Shoklo Malaria Research Unit
Academic Medical Centre, University of Amsterdam
Mahidol University
Australian Army Malaria Institute
John Radcliffe Hospital
Keywords: Medicine;Pharmacology, Toxicology and Pharmaceutics
Issue Date: 1-Sep-1999
Citation: European Journal of Clinical Pharmacology. Vol.55, No.6 (1999), 469-474
Abstract: Objective: Atovaquone plus proguanil is a new, well-tolerated and highly effective antimalarial drug. In order to protect it from the development of resistance, it may be deployed in combination with an artemisinin derivative. To investigate whether artesunate affects the pharmacokinetics of atovaquone plus proguanil, and to provide preliminary information regarding the tolerability of the triple drug combination (artesunate plus atovaquone plus proguanil), a cross over study was conducted in adult volunteers. Methods: Twelve healthy Karen adults were randomised to receive atovaquone-proguanil (1000/400 mg) with or without artesunate (250 mg) and, at least 90 days later, the study was repeated. Blood was sampled over a 10-day period. Results: The three-drug combination was well tolerated. Artesunate did not alter the pharmacokinetic properties of atovaquone and proguanil (maximum plasma concentrations: 13.02 μg/ml and 742 ng/ml; elimination half-lives: 42.2 h and 14.4 h; oral plasma clearance estimates: 90 ml/h/kg and 710 ml/h/kg; and apparent volumes of distribution: 4.9 l/kg and 14.5 l/kg, respectively). There was also no effect of artesunate on the biotransformation of proguanil to cycloguanil. The pharmacokinetic variables were similar to those reported previously for the individual drugs. Conclusion: Artesunate does not influence atovaquone or proguanil pharmacokinetics. The triple-drug combination of atovaquone and proguanil and artesunate was well tolerated.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0032796920&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/25599
ISSN: 00316970
Appears in Collections:Scopus 1991-2000

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