Bressolle F, Bres J, Faure A, Pistre M C
Eur J Drug Metab Pharmacokinet. 1986 Jul-Sep;11(3):165-70. doi: 10.1007/BF03189843.
The relative bioavailability of 100 mg canrenone capsules and the commercial 50 mg capsules has been determined in 12 healthy male subjects. The study was conducted in a cross over design. After the absorption phase canrenone plasma concentrations followed a biexponential decay. The half lives of the three phases observed were respectively 40.7 +/- 21.7 min, 1.94 +/- 0.558 hr and 18.5 +/- 3.93 hr after administration of a 100 mg capsules; they were respectively 31.8 +/- 14 min, 1.64 +/- 0.513 hr and 16.1 +/- 3.09 hr after administration of two 50 mg capsules. These values were similar to those reported in man. Bioequivalence of the two forms tested was ascertained by a two way analysis of variance and by the Westlake symmetrical confidence interval (95%). Peak plasma levels, Cmax, time to reach the peak, tmax, and the rate constant of absorption showed great inter and intra individual variations. In vivo hydrolysis of canrenone into canrenoic acid and subsequent lactonization of the acid are pH-dependent and could give rise to these variations if occurring before absorption.
在12名健康男性受试者中测定了100毫克坎利酮胶囊与市售50毫克胶囊的相对生物利用度。该研究采用交叉设计进行。吸收阶段后,坎利酮血浆浓度呈双指数衰减。服用100毫克胶囊后,观察到的三个阶段的半衰期分别为40.7±21.7分钟、1.94±0.558小时和18.5±3.93小时;服用两粒50毫克胶囊后,它们分别为31.8±14分钟、1.64±0.513小时和16.1±3.09小时。这些值与在人体中报道的值相似。通过双向方差分析和韦斯特莱克对称置信区间(95%)确定了两种受试剂型的生物等效性。血浆峰值水平(Cmax)、达到峰值的时间(tmax)和吸收速率常数显示出个体间和个体内的巨大差异。坎利酮在体内水解为坎利酸,随后该酸内酯化,这取决于pH值,如果在吸收前发生,可能会导致这些差异。