METABOLISM OF A NEW SYNTHETIC PROGESTAGEN, ORG-2969, IN FEMALE VOLUNTEERS - PHARMACOKINETICS AFTER AN ORAL DOSE

被引:27
作者
VIINIKKA, L
YLIKORKALA, O
VIHKO, R
WIJNAND, HP
BOOIJ, M
VANDERVEEN, F
机构
[1] UNIV OULU, DEPT CLIN CHEM, SF-90220 OULU 22, FINLAND
[2] UNIV OULU, DEPT OBSTET & GYNAECOL, SF-90220 OULU 22, FINLAND
[3] ORGANON SCI DEV GRP, ORGANON SCI DEV GRP, OSS, NETHERLANDS
[4] AKZO RES LABS, ANALOGUE COMP SECT, ARNHEM, NETHERLANDS
关键词
contraception; progestational steroid; radioimmunoassay;
D O I
10.1007/BF00558439
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The pharmacokinetics of a new synthetic progestagen, Org 2969 (13-ethyl-11-methylene-18,19-dinor-17α-pregn-4-en-20-yn-17-ol) and its presumed active metabolite, 3-keto-Org 2969, were studied in five healthy female volunteers. During the first part of the study (Phase I), four volunteers ingested as a single dose 50 μg (about 100 μCi) of [16-3H]-Org 2969 together with 50 μg of ethinyl oestradiol. During the second part (Phase II), ten days of pretreatment with non-readioactive Org 2969 and ethinyl oestradiol preceded dosing, which was similar to that in Phase I. The fifth volunteer ingested 2500 μg of Org 2969 as a single dose. The concentrations of Org 2969 and 3-keto-Org 2969 in serum were measured by specific radioimmunoassay, and by as radioactivity. The maximum serum level of Org 2969 of 0.2-0.3% of the dose/litre was obtained 0.8-1.3 h after administration, and it was followed by a mono-exponential decrease, the half-life being 1.3-1.5 hours. No difference in Org 2969 levels was seen between Phase I and Phase II studies. The maximum 3-keto-Org 2969 serum level in Phase I was 0.4-0.8% of the dose/litre, 1-3 h after administration. A two-compartment open body model adequately described the data. The half-life of elimination was 16 hours. There was a considerable change in the single dose kinetics between Phase I and Phase II in the case of 3-keto-Org 2969. In Phase II the maximum serum level was 2.0-3.4% of the dose/litre, and there was no significant change in half-life. The change was considered to be due to a decrease in the apparent volume of distribution as a result of an increased number of binding sites on sex hormone-binding globulin induced by ethinyl oestradiol during the pretreatment period, and/or to an increase in the fraction of Org 2969 metabolized to 3-keto-Org 2969. The two simultaneous processes contributed to the change in kinetics and to the production of a steady state level of 3-keto-Org 2969 which resulted in a steady state within the first 10 days of daily administration of Org 2969 and ethinyl oestradiol. © 1979 Springer-Verlag.
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页码:349 / 355
页数:7
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