Schulz V
Arzneimittelforschung. 1976 Apr;26(4):544-6.
13 female rhesus monkeys were given 2'-14C-cyproterone acetate i.v. and p.o. The radioactivity of the blood plasma and the elimination in urine and faeces were then measured at suitable intervals for a period of 12 days. After i.v. administration the time for distribution in the body amounted to 8 h. The extrapolated initial concentrations in the equilibrium to distribution amounted to 0.68% of the administered dose in the plasma volume, and the theoretical volume of distribution was 5 times the body volume. After oral administration the maximum levels in the plasma were reached on an average 13 h after administration. They attained the level of the extrapolated initial concentration after i.v. administration. The compound was eliminated from the body with a radioactive half-life of 1.6 to 1.8 days, irrespective of the route of administration. The mean ratio of elimination urine: faeces was approximately 0.7 for all animals. After oral administration 81% of the dose was absorbed on the average.
给13只雌性恒河猴静脉注射和口服2'-14C-醋酸环丙孕酮。然后在12天的时间内,每隔适当的时间间隔测量血浆中的放射性以及尿液和粪便中的排泄情况。静脉注射后,体内分布时间为8小时。外推的平衡分布初始浓度相当于给药剂量在血浆体积中的0.68%,理论分布容积为身体体积的5倍。口服给药后,血浆中平均在给药后13小时达到最高水平。它们达到了静脉注射后外推的初始浓度水平。无论给药途径如何,该化合物从体内消除的放射性半衰期为1.6至1.8天。所有动物尿液与粪便的平均排泄比约为0.7。口服给药后,平均81%的剂量被吸收。