Chloroquine pharmacokinetics in pregnant and nonpregnant women with vivax malaria
Lee, S.J.; McGready, R.; Fernandez, C.; Stepniewska, K.; Paw, M.K.; Viladpai-nguen, S.J.; Thwai, K.L.; Villegas, L.; Singhasivanon, P.; Greenwood, B.M.; White, N.J.; Nosten, F.ço.
European Journal of Clinical Pharmacology 64(10): 987-992
2008
ISSN/ISBN: 1432-1041 PMID: 18594802 DOI: 10.1007/s00228-008-0500-zDocument Number: 203395
We compared the pharmacokinetics of chloroquine in pregnant and nonpregnant women treated for Plasmodium vivax malaria. Twelve pregnant women and 15 nonpregnant women of child-bearing age with acute P. vivax malaria were treated with 25 mg chloroquine base/kg over 3 days on the northwestern border of Thailand. Blood concentrations of chloroquine and desethylchloroquine were measured using hydrophilic interaction liquid chromatography coupled with fluorescence detection. Twenty-five women completed the pharmacokinetic study. Although increasing gestational age was associated with reduced chloroquine AUC0-->infinity, there was no significant difference overall in the pharmacokinetics of chloroquine between pregnant and nonpregnant women. Fever was associated with lower chloroquine AUC0-->infinity values. Desethylchloroquine area under the curve (AUC) values were not significantly affected by pregnancy. Pregnancy did not significantly affect blood concentrations of chloroquine or its metabolite, desethylchloroquine, in women with P. vivax malaria.