Malspeis L, Bathala M S, Ludden T M, Bhat H B, Frank S G, Sokoloski T D, Morrison B E, Reuning R H
Res Commun Chem Pathol Pharmacol. 1975 Sep;12(1):43-65.
Reduction of naltrexone and naloxone with sodium borohydride gave a mixture (85:15) of the 6alpha- and 6beta-hydroxy epimers, alpha- and beta-naltrexol and alpha- and beta-naloxol, respectively. Each pair of epimers was separated by preparative thin-layer chromatography and the physical and spectral properties of each compound were determined. Previous assignments for the configuration of the epimers were verified. A semi-quantitative electron capture gas-liquid chromatographic method was devised for distinguishing either alpha- or beta-naltrexol in the presence of the other and in the presence of large amounts (at least 10-fold greater) of naltrexone. The method was used to determine the approximate weight ratio of beta-naltrexol to naltrexone present in enzymatically hydrolyzed urine samples. It was found that substantially greater quantities of beta-naltrexol and/or its conjugates were excreted in the urine of man, monkey, guinea pig and rabbit after administration of naltrexone, whereas very small quantities were excreted by the mouse, rat and dog. In contrast, just trace amounts of the 6alpha-hydroxy epimer, alpha-naltrexol, were detected in the urine of only 2 of the 7 species that had received naltrexone, i.e., monkey and guinea pig. After administration of 3H-15,16-naltrexone, 1 mg/kg, i.v. to the guinea pig, 25% of the radioactivity found following thin-layer chromatography of the extract of acid-hydrolyzed urine corresponded to beta-naltrexol. In gall bladder bile from the guinea pig, only conjugates of naltrexone and beta-naltrexol were found 2 hours after administration of naltrexone. Following administration of beta-naltrexol, 1 mg/kg, i.v. to guinea pigs only beta-naltrexol and/or its conjugates were detected in urine or bile. However, urine collected after administration of alpha-naltrexol, 1 mg/kg, i.v. to guinea pigs contained alpha-naltrexol and its conjugates, as well as a yet unidentified metabolite.
用硼氢化钠还原纳曲酮和纳洛酮得到了分别为6α-和6β-羟基差向异构体、α-和β-纳曲醇以及α-和β-纳洛醇的混合物(85:15)。每对差向异构体通过制备型薄层色谱法进行分离,并测定了每种化合物的物理和光谱性质。验证了之前对差向异构体构型的归属。设计了一种半定量电子捕获气液色谱法,用于在存在另一种异构体以及存在大量(至少大10倍)纳曲酮的情况下区分α-或β-纳曲醇。该方法用于测定酶水解尿液样品中β-纳曲醇与纳曲酮的近似重量比。结果发现,给予纳曲酮后,人、猴、豚鼠和兔的尿液中排泄出的β-纳曲醇和/或其结合物的量显著增加,而小鼠、大鼠和狗排泄的量非常少。相比之下,在接受纳曲酮的7种动物中,只有2种动物(即猴和豚鼠)的尿液中检测到微量的6α-羟基差向异构体α-纳曲醇。给豚鼠静脉注射1mg/kg的3H-15,16-纳曲酮后,酸水解尿液提取物经薄层色谱分析后发现,25%的放射性对应于β-纳曲醇。在豚鼠的胆囊胆汁中,给予纳曲酮2小时后仅发现纳曲酮和β-纳曲醇的结合物。给豚鼠静脉注射1mg/kg的β-纳曲醇后,在尿液或胆汁中仅检测到β-纳曲醇和/或其结合物。然而,给豚鼠静脉注射1mg/kg的α-纳曲醇后收集的尿液中含有α-纳曲醇及其结合物,以及一种尚未鉴定的代谢产物。