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人口服泛普法宗后甲基苯丙胺的血浆和尿液浓度。

Plasma and urinary concentrations of methamphetamine after oral administration of famprofazone to man.

作者信息

Oh E S, Hong S K, Kang G I

机构信息

College of Pharmacy, Sookmyung Women's University, Seoul, Korea.

出版信息

Xenobiotica. 1992 Mar;22(3):377-84. doi: 10.3109/00498259209046649.

Abstract
  1. To obtain further evidence for the metabolic formation of methamphetamine from famprofazone in man, concentrations of methamphetamine in plasma, as well as in urine, were measured by g.l.c. In addition, intact famprofazone and famprofazone N-oxide were analysed in the urine. 2. Methamphetamine appeared in plasma 1 h after a single 100 mg dose of the drug to two male subjects, and the concentration maintained between 24 and 44 ng/ml over 2-12 h, declining to 10 ng/ml and an undetectable level respectively after 24 h. 3. Total urinary excretion of methamphetamine over 72 h was 1.9 mg for a 25 mg dose and 2.2 mg for a 50 mg dose. After a 100 mg dose, 4.6 mg of methamphetamine was excreted over 36 h. Neither intact famprofazone nor famprofazone N-oxide were detected when the urine samples after the 100 mg dose were examined. 4. The results provide further evidence that methamphetamine is a bona fide human metabolite of famprofazone and suggest that at least 20% dose may be broken down via the pathways leading to the formation of methamphetamine. This could have significant clinical implications as the result of pharmacological activity of this metabolite.
摘要
  1. 为了获得更多关于人体内法莫替丁代谢生成甲基苯丙胺的证据,通过气相色谱法测定了血浆和尿液中甲基苯丙胺的浓度。此外,还对尿液中的完整法莫替丁和法莫替丁N -氧化物进行了分析。2. 给两名男性受试者单次服用100毫克该药物后1小时,血浆中出现了甲基苯丙胺,其浓度在2至12小时内维持在24至44纳克/毫升之间,24小时后分别降至10纳克/毫升和检测不到的水平。3. 25毫克剂量时,72小时内甲基苯丙胺的总尿排泄量为1.9毫克;50毫克剂量时为2.2毫克。100毫克剂量后,36小时内排泄出4.6毫克甲基苯丙胺。检测100毫克剂量后的尿液样本时,未发现完整的法莫替丁和法莫替丁N -氧化物。4. 这些结果提供了更多证据,表明甲基苯丙胺是法莫替丁真正的人体代谢产物,并表明至少20%的剂量可能通过导致甲基苯丙胺形成的途径分解。由于这种代谢产物的药理活性,这可能具有重要的临床意义。

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