Delbeke F T, Debackere M
Biopharm Drug Dispos. 1981 Jan-Mar;2(1):17-30. doi: 10.1002/bdd.2510020103.
A gas-chromatographic (g.l.c.) method with electron-capture (e.c.) detection is described for the simultaneous quantitative determination of nanogram concentrations of 2-ethylamino-3-phenyl-norbornane (Fencamfamine, REACTIVAN) and its metabolite 2-amino-3-phenylnorbornane in urine. The renal excretion of fencamfamine and its metabolite after oral administration to humans was followed over a period of several days. The excretion of both substances was affected by urinary pH. Excretion peaks were obtained 2-4 h after ingestion and the total amount excreted during 80 h varied from 11.9 to 33.2 per cent. Based on urinary values, the biological half life of fencamfamine was 16 h. The intake of acetazolamide shortly after fencamfamine resulted in a decrease of the fencamfamine excretion and a suppression of the metabolite output during at least 10 h. Acetazolamide did not influence the percentage of the doses excreted during 80 h. No changes occurred in urinary fencamfamine or metabolite concentrations during storage of urine at -18 degrees for 6 weeks.
本文描述了一种采用电子捕获检测的气相色谱法,用于同时定量测定尿液中纳克浓度的2-乙氨基-3-苯基降冰片烷(芬坎法明,瑞他命)及其代谢物2-氨基-3-苯基降冰片烷。对人体口服芬坎法明后,其及其代谢物在数天内的肾脏排泄情况进行了跟踪。两种物质的排泄均受尿液pH值影响。摄入后2 - 4小时出现排泄峰值,80小时内排泄总量在11.9%至33.2%之间变化。根据尿液值,芬坎法明的生物半衰期为16小时。在芬坎法明摄入后不久服用乙酰唑胺,导致芬坎法明排泄减少,并在至少10小时内抑制代谢物的排出。乙酰唑胺不影响80小时内排泄剂量的百分比。尿液在-18℃储存6周期间,尿液中芬坎法明或代谢物浓度无变化。