Ishida T, Yano M, Toki S
Faculty of Pharmaceutical Sciences, Fukuoka University, Japan.
J Anal Toxicol. 1998 Nov-Dec;22(7):567-72. doi: 10.1093/jat/22.7.567.
Codeinone-glutathione adduct (CO-GSH) in the bile of guinea pigs given a subcutaneous injection of codeine was isolated and identified. Synthesized authentic CO-GSH was characterized by the mass and nuclear magnetic resonance spectra and used as the standard sample. The metabolite was isolated by preparative high-performance liquid chromatography on a C18 column. The fractions containing the conjugated metabolite were purified using Sep-Pak C18 cartridges. For further purification of the metabolite CO-GSH, a Radial Pak CN column was used. Structure assignment of the metabolite was then performed by fast-atom-bombardment mass spectrometry and 500 MHz Fourier-transform-NMR spectrometric analysis and identified as S-[4,5-epoxy-3-methoxy-17-methyl-6-oxomorphinan-(8S)-yl] glutathione.
对皮下注射可待因的豚鼠胆汁中的可待因酮 - 谷胱甘肽加合物(CO - GSH)进行了分离和鉴定。通过质谱和核磁共振光谱对合成的纯品CO - GSH进行了表征,并用作标准样品。代谢产物通过在C18柱上的制备型高效液相色谱法进行分离。含有共轭代谢产物的馏分使用Sep - Pak C18柱进行纯化。为了进一步纯化代谢产物CO - GSH,使用了Radial Pak CN柱。然后通过快原子轰击质谱和500 MHz傅里叶变换核磁共振光谱分析对代谢产物进行结构鉴定,并确定为S - [4,5 - 环氧 - 3 - 甲氧基 - 17 - 甲基 - 6 - 氧代吗啡喃 - (8S) - 基]谷胱甘肽。