Tse F L, Ballard F, Jaffe J M
J Pharm Sci. 1983 Mar;72(3):311-2. doi: 10.1002/jps.2600720327.
The excretion of temazepam and its N-desmethyl metabolite, oxazepam, and their respective O-conjugates was examined following a single intravenous dose of [14C]temazepam to two groups of bile fistula rats, with and without bile replenishment to the animals via duodenal cannulae. During an 8-hr collection period, the two groups produced virtually identical bile volumes, and there were no significant differences between them in the amount of total radioactivity, free temazepam, or the identified metabolites in the bile, as determined by TLC and liquid scintillation counting. Elimination of the radioactive dose was rapid during 0-8 hr, with a half-life of approximately 1 hr. Approximately 85-90% of the administered radioactivity was recovered in the bile: less than 1% as free temazepam, 3% as oxazepam, and approximately 10% as their O-conjugates.
给两组胆瘘大鼠单次静脉注射[14C]替马西泮后,研究了替马西泮及其N - 去甲基代谢产物奥沙西泮以及它们各自的O - 共轭物的排泄情况,一组通过十二指肠插管向动物补充胆汁,另一组不补充。在8小时的收集期内,两组产生的胆汁量几乎相同,通过薄层色谱法(TLC)和液体闪烁计数法测定,两组胆汁中的总放射性、游离替马西泮或已鉴定代谢产物的量没有显著差异。在0 - 8小时内放射性剂量的消除很快,半衰期约为1小时。约85 - 90%的给药放射性在胆汁中回收:游离替马西泮不到1%,奥沙西泮为3%,其O - 共轭物约为10%。