Paintaud G, Alván G, Ericsson O
Department of Clinical Pharmacology, Karolinska Institute, Sweden.
Br J Clin Pharmacol. 1993 Mar;35(3):305-7. doi: 10.1111/j.1365-2125.1993.tb05698.x.
Plasma concentrations of quinine were measured in six healthy volunteers after a duplicate administration of 15 mg kg-1 of quinine hydrochloride orally and the administration of 15 mg kg-1 of quinine dihydrochloride as an infusion over 6 h. Quinine absorption rate devised by deconvolution was shown to be complete in less than 2 h. The mean (+/- s.d.) fraction available (F) was 0.76 (0.11) after both oral doses and maximum plasma drug concentrations occurred at 1.90 (0.83) h and 2.00 (0.30) h, respectively. The reproducibility of absorption was high, with a within-subject coefficient of variation of less than 10% for Cmax, AUC and F. Thus, quinine absorption is extensive, fast and reproducible in healthy volunteers.
在六名健康志愿者口服重复给予15 mg/kg盐酸奎宁并静脉输注15 mg/kg二盐酸奎宁6小时后,测定了血浆奎宁浓度。通过反卷积法得出的奎宁吸收率显示在不到2小时内即可完全吸收。两次口服给药后的平均(±标准差)可利用分数(F)为0.76(0.11),最大血浆药物浓度分别出现在1.90(0.83)小时和2.00(0.30)小时。吸收的重现性很高,Cmax、AUC和F的受试者内变异系数均小于10%。因此,在健康志愿者中,奎宁吸收广泛、迅速且具有重现性。