| Literature DB >> 7285572 |
K Fotherby, J Akpoviroro, H A Abdel-Rahman, H K Toppozada, J C de Souza, E M Coutinho, S Koetsawang, P Nukulkarn, U K Sheth, M K Mapa, S Gopalan, E R Plunkett, P F Brenner, M V Hickey, E S Grech, R Lichtenberg, C Gual, R Molina, C Gomez-Rogers, E Kwon, S W Kim, T Chan, S S Ratnam, B M Landgren, R P Shearman, J W Goldzieher, T S Dozier.
Abstract
The pharmacokinetics of a dose of 50 microgram ethynyloestradiol administered orally was studied in fourteen centres. Absorption was rapid and the highest serum concentrations of total ethynyloestradiol were found in most subjects at 1 h and by 24 h concentrations were less than 250 pg/ml. Calculation of the half-lives for absorption, distribution and elimination showed wide variations between subjects, the half-life of elimination varying from 2.5 h to more than 30 h. Bioavailability as measured by the area under the serum ethynyloestradiol concentration-time curve also showed more than a ten-fold variation. Intra-centre differences in the various parameters measured were as large as the inter-centre differences.Entities:
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Year: 1981 PMID: 7285572 DOI: 10.1016/0010-7824(81)90076-7
Source DB: PubMed Journal: Contraception ISSN: 0010-7824 Impact factor: 3.375