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Pharmacokinetics, tissue distribution, and excretion of nomegestrol acetate in female rats.
- Source :
- European Journal of Drug Metabolism & Pharmacokinetics; Dec2015, Vol. 40 Issue 4, p435-442, 8p
- Publication Year :
- 2015
-
Abstract
- Nomegestrol acetate (NOMAC), a synthetic progestogen derived from 19-norprogesterone, is an orally active drug with a strong affinity for the progesterone receptor. NOMAC inhibits ovulation and is devoid of undesirable androgenic and estrogenic activities. The aim of this study was to evaluate the pharmacokinetics, tissue distribution, and excretion of NOMAC in female rats. Sprague-Dawley female rats were orally administered a single dose of NOMAC (10, 20 or 40 mg/kg) and drug plasma concentrations at different times were determined by RP-HPLC. Tissue distribution at 1, 2, and 4 h and excretion of NOMAC into bile, urine, and feces after dosing were investigated. The results showed that NOMAC was rapidly absorbed after oral administration, with $$t_{ \hbox{max} }$$ of 1-2 h. The plasma concentration-time curves were fitted in a two-compartment model. The exposure to NOMAC ( $$C_{ \hbox{max} }$$ and $${\text{AUC}}$$ ) increased dose proportionally from 10 to 40 mg/kg. The average CL and $$t_{1/2\beta }$$ were 5.58 L/(h·kg) and 10.8 h, respectively. The highest concentrations of NOMAC in ovary, liver, kidney, lung, heart, brain, spleen, muscle, and uterus were observed at 2 h, whereas the highest concentrations in stomach, pituitary, and hypothalamus appeared at 1 h. The total cumulative excretion of NOMAC in feces (0-72 h), urine (0-72 h), and bile (0-48 h) was ~1.06, 0.03, and 0.08 % of the oral administered dose, respectively. This study indicated that NOMAC had a widespread distribution in tissues, including ovary, pituitary, and hypothalamus, which are main target tissues where NOMAC inhibits ovulation. NOMAC was excreted via both feces and urine with few unchanged NOMAC excreted. Enterohepatic circulation was found in the drug elimination; however, it did not significantly affect $$t_{ \hbox{max} }$$ . [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 03787966
- Volume :
- 40
- Issue :
- 4
- Database :
- Complementary Index
- Journal :
- European Journal of Drug Metabolism & Pharmacokinetics
- Publication Type :
- Academic Journal
- Accession number :
- 111160108
- Full Text :
- https://doi.org/10.1007/s13318-014-0224-7