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H Ek

Publications and source records attributed to H Ek.

5 recordsLinked to original sources

Detection and quantitation of 3 alpha-hydroxy-1-methylen-5 alpha-androstan-17-one, the major urinary metabolite of methenolone acetate (Primobolan) by isotope dilution--mass spectrometry.

A highly accurate method has been developed for detection and quantitation of 3 alpha-hydroxy-1-methylen-5 alpha-androstan-17-one, the major urinary metabolite of methenolone acetate (Primobolan) in man. Unlabelled as well as 2H-labelled 3 alpha-hydroxy-1-methylen-5 alpha-androstan-17-one were synthesized from 1-methylen-5 alpha-androstane-3,17-dione. A fixed amount of the internal standard was added to a fixed amount of urine and the mixture was treated with Helix pomatia for 24 h. After extraction and purification by t.l.c., the mixture was converted into methoxime--trimethylsilyl derivative and analyzed by combined GC--MS. Unlabelled 3 alpha-hydroxy-1-methylen-5 alpha-androstan-17-one could be quantitated from the ratio between the tracings of the ions at m/z 372 and m/z 375 (corresponding to the M-31 ions). In alternative procedures, the ions at m/z 403 and m/z 406 (molecular ions) as well as m/z 282 and m/z 285 (M-90-31 ions) could be used. Under the conditions employed, the metabolite could be identified and quantitated in concentrations exceeding 10 ng/ml. Significant amounts of the metabolite could be detected in urine during 5 days after a single oral ingestion of 10 mg of Primobolan. The method has been successfully used for analyses of urine samples obtained from athletes involved in competition.

Deuterium↗

Detection and quantitation of 19-norandrosterone in urine by isotope dilution-mass spectrometry.

A highly accurate method has been developed for detection and quantitation of 19-norandrosterone, the major urinary metabolite of 19-nortestosterone in man. A suitable 14C labelled standard was obtained by i.m. injection of [4-14C]-19-nortestosterone into a human volunteer. A fixed amount of this internal standard was added to a fixed amount of urine and the mixture was treated with Helix pomatia for 24 h. After extraction and purification by t.l.c., the mixture was converted into methoxime-trimethylsilyl derivative and analyzed by combined GC-MS. Unlabelled 19-norandrosterone could be quantitated from the ratio between the tracings of the ions at m/z 256 and m/z 258, corresponding to M-90-31 ions. In alternative procedures the ions at m/z 346 and 348 (corresponding to the M-31 ions) could be used. Under the conditions employed, urinary 19-norandrosterone could be identified and quantitated in concentrations exceeding 20 ng/ml. The steroid could be traced in urine up to 6 weeks after i.m. administration of 25 mg of the decanoate of 19-nortestosterone (Deca-Durabol). When using radioimmunoassay with antibodies towards unmetabolized 19-nortestosterone, it was possible to trace urinary 19-nortestosterone only for 1-2 weeks after the administration. The present method has been successfully used for analysis of 19-norandrosterone in urine samples obtained from athletes involved in competition.

Estranes↗