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Gas Chromatographic/Mass Spectrometric Characterization of Dromostanolone Metabolites in Human Urine


Abstract

The metabolism of dromostanolone (2α-methyl-5α- androstan-17β-ol-3-one) was studied in three adult volunteers after oral dose of 20 mg. Solvent extracts of urine obtained after enzyme hydrolysis were derivatized with MSTFA/TMCS and MSTFA/TMIS. The structures of intact drug and its metabolites were determined by gas chromatography/mass spectrometry (GC/MS) in electron impact (EI) mode. The major metabolite (2α-methyl-5α- androstan-3α-ol-17-one), its 3β-epimer, parent compound, and several hydroxylated metabolites including intact drug were detected by comparing total ion chromatograms of control urine with that of the administered sample. Two epimers of 2α-methyl-5α- androstan-3,17β-diol were detected using selected ion monitoring. The maximum excretion of dromostanolone and 2α-methyl-5α- androstan-3α-ol-17-one was reached in 6.2-15 hr. The half-life of intact dromostanolone was 5.3 hr. About 3.0% of the administered amount was found to be excreted within 95 hr as unchanged form.

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References

  1. J. Clin. Nutr. v.27 Choi, S. K.;Chung, T. J.;Morrison, R. S.;Myers, C.;Greenberg, M. S.
  2. Cancer Chemotheraphy Reports v.56 Seay, D. G.;Bradshaw, J. D.;Nicol, N. T.
  3. Arzneimittel-Forsch v.16 Gehard, E.;Gibian, H.;Kolb, K. H.
  4. Wien, Klin. Wochenschr. v.7 Huck, H.;Egg, D.
  5. J. High. Resol. Chromato. Commun. v.8 Cartoni, G. P.;Giarruso, A.;Ciardi, M.;Rosati, C.
  6. Anal. Chim. Acta. v.275 Schanzer, W.;Donike, M.
  7. J. Steroid Biochem. Molec. Biol. v.42 De Boer, D.;De Jong, E. G.;Maes, R. A. A.;van Rossum, J. M.
  8. Steroids v.29 Templeton, J.;Kim, R. S.
  9. J. Chromatogr. v.202 Donike, M.;Zimmerman, J.
  10. J. Chromatogr. v.489 Masse, R.;Ayotte, C.;Dugal, R.
  11. J. Chromatogr. v.479 Houghton, E.;Ginn, A.;Teale, P.;Minoo, C.;Copsey, J.