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   <subfield code="a">Stereoselective pharmacokinetics of mefloquine in young children</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[A. Bourahla, C. Martin, F. Gimenez, V. Singhasivanon, P. Attanath, A. Sabchearon, T. Chongsuphajaisiddhi, R. Farinotti]</subfield>
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   <subfield code="a">Objective: the stereospecificity of mefloquine pharmacokinetics in children has been investigated. Patients: Twelve children aged 6 to 24 months were treated for uncomplicated falciparum malaria with a single oral dose of 25 mg⋅kg−1 racemic mefloquine in combination with sulfadoxine and pyrimethamine. Methods: concentrations of mefloquine enantiomers were determined using a coupled achiral-chiral chromatographic system. Pharmacokinetic parameters were calculated using model-independent analysis. Results: Maximum plasma concentrations, areas under the curve and apparent plasma elimination half-lives were higher for the (−) enantiomer than its antipode. In contrast, the apparent volume of distribution (V/f) and total clearance (Cl/f) values were higher for the (+) enantiomer. Conclusion: the stereoselectivity of mefloquine pharmacokinetics is similar to that observed in adults.</subfield>
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   <subfield code="a">Key words Mefloquine</subfield>
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