人胆汁中罗红霉素代谢产物的研究  

STUDIES ON METABOLITES OF ROXITHROMYCIN IN HUMAN BILE

作　　者：李雪庆[1,2] 钟大放[1,2] 吴硕东[1,2] 王爱民[1,2] 田蕾[1,2] 于宏 

机构地区：[1]沈阳药科大学药物代谢与药物动力学实验室 [2]中国医科大学第二附属医院

出　　处：《药学学报》1999年第1期49-53,共5页Acta Pharmaceutica Sinica

基　　金：国家自然科学基金

摘　　要：目的：研究人胆汁中罗红霉素的代谢转化产物。方法：采用高效液相色谱离子阱质谱法，对患者ｐｏ罗红霉素后的胆汁样品进行了分析。结果：发现了１３个代谢产物，分别为罗红霉素的（９Ｚ）异构体及其（９Ｅ），（９Ｚ）Ｎ去甲基和Ｎ双去甲基衍生物和（９Ｅ）及（９Ｚ）脱克拉定糖衍生物，（９Ｅ）和（９Ｚ）红霉素肟及其（９Ｅ）和（９Ｚ）Ｎ去甲基及Ｎ双去甲基衍生物，其中９种为新发现的代谢物。AIM: To study the metabolites of roxithromycin (RXM) in the bile of a patient, who had received an oral dose of 150 mg RXM after gallbladder operation. METHODS: High performance liquid chromatography/ion trap mass spectrometry was used to determinate RXM and its metabolites in human bile. The bile sample was collected, extracted with diethyl ether and separated on a C 18 reversed phase column with (+)ESI MS n detection. RESULTS: RXM and its thirteen metabolites were identified in the sample based on reference substances and mass spectra. These include descladinose RXM (M1), erythromycin oxime (M2) and its N mono and N didemethylated derivatives (M4 and M6), N mono and didemethylated derivatives of RXM (M3 and M5), as well as the (9 Z ) epimeric isomers of RXM and all its above metabolites (M7～M13). The ratios of (9 Z ) to (9 E ) isomers were found to be between 0 11～0 79. The parent drug remained was about 20% of the total bile metabolites. CONCLUSION: The metabolic pathways of RXM observed in the human bile are therefore quite different to those in human plasma and urine. The identification of the isomerization of the oximes of RXM derivatives represents a novel biotransformation pathway.

关 键 词：罗红霉素 人胆汁 高效液相色谱法-离子阱质谱法 药代动力学 几何异构化 药物代谢物 

分 类 号：R969.1[医药卫生—药理学] R978.[医药卫生—药学]