British Journal of Clinical Pharmacology · 1991 · 23 citations · 11 references
PharmacyPharmacokineticsPharmacologyBioavailabilityContraceptionDrug ClearanceContraceptive PharmacotherapyDrug DispositionDrug Half-lifeHalf-life EstimationReproductive PharmacologySex-based Pharmacokinetic DifferencesControl Group DesignDrug Elimination Half-lifeMatched Control GroupOral Contraceptive EffectsOral Contraceptive PillsOral Drug ClearancePharmacokinetic ParametersPharmacokinetics Of Hormonal Contraceptives
The pharmacokinetics of quinine after a single 600 mg oral dose of quinine sulphate were studied in seven female subjects who used oral contraceptives and in seven age-matched female controls who did not. There were no significant differences (P greater than 0.05) in the maximum plasma concentration (Cmax) and the time of peak concentration (tmax) between the subjects who used oral contraceptives (Cmax = 5.3 +/- 1.0 (s.d.) mg l-1; tmax = 1.4 +/- 0.7 h) and the control subjects (Cmax = 5.6 +/- 0.9 mg l-1; tmax = 2.1 +/- 0.9 h). The mean elimination half-life of quinine in the oral contraceptives user group (12.5 +/- 1.9 h) was similar (P greater than 0.05) to that in the control group (11.8 +/- 2.7 h). The oral clearance of quinine in the oral contraceptive user group was 0.133 +/- 0.055 l h-1 kg-1 (range 0.073-0.233) and was not significantly different (P greater than 0.05) from that observed in the control group (0.125 +/- 0.025 l h-1 kg-1, range 0.075-0.148).
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F. Peter Guengerich, M V Martin, Philippe Beaune et al. · Journal of Biological Chemistry · 1986 · 730 citations · Full text
Medicine, Biochemistry, Pharmacology +17
Pornthep Chanthavanich, Sanjeev Krishna, C Bunch et al. · British Journal of Clinical Pharmacology · 1983 · 67 citations · Full text