Anggård E, Nilsson M I, Holmstrand J, Gunne L M
Eur J Clin Pharmacol. 1979 Aug;16(1):53-7. doi: 10.1007/BF00644967.
A technique is presented for study of steady state kinetics of methadone using pulse labeling with deuterated methadone (d3) and mass fragmentography to measure both unlabeled and labeled methadone in blood. Seven subjects maintained on methadone for at least 10 months were admitted to a closed metabolic ward. The daily dose of unlabeled methadone (d0) was substituted by one dose of methoadone-d3 and plasma levels of methadone-d0 and methadone-d3 were followed for 48 h using a precise (SD +/- 5%) and sensitive (30 pmol/ml) mass fragmentographic technique. Plasma half-lives (T1/2) for both methadone-do and methadone-d3 were calculated from samples obtained 8--24 H following the dose of methadone-d3. The t1/2 of oral methadone-d3 was shorter (22 +/- 2 h) than that of methadone-d0 (52 +/- 20 h). The same pattern was observed after intravenous administration. The results indicate multiple pools of methadone in the body.
本文介绍了一种研究美沙酮稳态动力学的技术,该技术使用氘代美沙酮(d3)脉冲标记和质量碎片分析法来测量血液中未标记和标记的美沙酮。七名服用美沙酮至少10个月的受试者被收治入一个封闭的代谢病房。用一剂美沙酮-d3替代未标记美沙酮(d0)的每日剂量,并使用精确(标准差±5%)且灵敏(30皮摩尔/毫升)的质量碎片分析技术跟踪美沙酮-d0和美沙酮-d3的血浆水平48小时。根据服用美沙酮-d3后8至24小时采集的样本计算美沙酮-d0和美沙酮-d3的血浆半衰期(T1/2)。口服美沙酮-d3的t1/2(22±2小时)比美沙酮-d0的t1/2(52±20小时)短。静脉给药后观察到相同的模式。结果表明体内存在多个美沙酮池。