Cone E J, Gorodetzky C W, Darwin W D, Carroll F I, Brine G A, Welch C D
Res Commun Chem Pathol Pharmacol. 1978 Jun;20(3):413-33.
Two metabolites of naltrexone were identified in human and rat urine following drug administration. The metabolites, 2-hydroxy-3-0-methylnatrexone and 2-hydroxy-3-0-methyl-6 beta-naltrexol, were identified by comparison of their respective gas chromatographic retention times and methane chemical ionization spectral patterns with authentic standards. The standards were obtained by chemical synthesis from naltrexone. Urinary excretion of the two metabolites was measured by single ion recording of the pseudomolecular ions of the metabolites and an internal standard. Excretion data was collected from 5 human subjects over a period of 5 days following a single dose of naltrexone. The metabolites, 2-hydroxy-3-0-methylnatrexone and 2-hydroxy-3-0-methyl-6 beta-natrexol were found to account for an average (+/- standard error) of 0.45 +/- 0.08% and 4.6 +/- 2.1% of the administered dose, respectively. An unusually long half-life of elimination of the latter metabolite (mean of 20.2 +/- 1.8 hr) was observed. Acid-hydrolysis of the samples failed to produce a significant increase of either metabolite indicating that the major protion of these metabolites is excreted in the free form.
给药后,在人和大鼠尿液中鉴定出纳曲酮的两种代谢物。通过将它们各自的气相色谱保留时间和甲烷化学电离光谱图与标准品进行比较,鉴定出代谢物2-羟基-3-O-甲基纳曲酮和2-羟基-3-O-甲基-6β-纳曲醇。这些标准品是通过纳曲酮化学合成获得的。通过对代谢物和内标物的准分子离子进行单离子记录来测定两种代谢物的尿排泄量。在单剂量给予纳曲酮后的5天内,从5名人类受试者收集排泄数据。发现代谢物2-羟基-3-O-甲基纳曲酮和2-羟基-3-O-甲基-6β-纳曲醇分别占给药剂量的0.45±0.08%和4.6±2.1%(平均值±标准误)。观察到后一种代谢物的消除半衰期异常长(平均为20.2±1.8小时)。样品的酸水解未使任何一种代谢物显著增加,表明这些代谢物的主要部分以游离形式排泄。