王春雪, 王玲, 钱大玮, 张黄琴, 黄文哲, 王团结, 朱振华, 宿树兰, 郭盛, 段金廒. 静脉给药热毒宁注射液大鼠血浆、胆汁、尿液和粪便中代谢产物的鉴定J. 药学学报, 2018,53(7): 1148-1155. doi: 10.16438/j.0513-4870.2018-0052
引用本文: 王春雪, 王玲, 钱大玮, 张黄琴, 黄文哲, 王团结, 朱振华, 宿树兰, 郭盛, 段金廒. 静脉给药热毒宁注射液大鼠血浆、胆汁、尿液和粪便中代谢产物的鉴定J. 药学学报, 2018,53(7): 1148-1155. doi: 10.16438/j.0513-4870.2018-0052
WANG Chun-xue, WANG Ling, QIAN Da-wei, ZHANG Huang-qin, HUANG Wen-zhe, WANG Tuan-jie, ZHU Zhen-hua, SU Shu-lan, GUO Sheng, DUAN Jin-ao. Identification of metabolites of Reduning injection in rat plasma, bile, urine and feces after intravenous administrationJ. Acta Pharmaceutica Sinica, 2018,53(7): 1148-1155. doi: 10.16438/j.0513-4870.2018-0052
Citation: WANG Chun-xue, WANG Ling, QIAN Da-wei, ZHANG Huang-qin, HUANG Wen-zhe, WANG Tuan-jie, ZHU Zhen-hua, SU Shu-lan, GUO Sheng, DUAN Jin-ao. Identification of metabolites of Reduning injection in rat plasma, bile, urine and feces after intravenous administrationJ. Acta Pharmaceutica Sinica, 2018,53(7): 1148-1155. doi: 10.16438/j.0513-4870.2018-0052

静脉给药热毒宁注射液大鼠血浆、胆汁、尿液和粪便中代谢产物的鉴定

Identification of metabolites of Reduning injection in rat plasma, bile, urine and feces after intravenous administration

  • 摘要: 研究热毒宁注射液在大鼠体内的代谢产物。采用超高效液相色谱-线性离子阱-静电轨道阱串联质谱联用方法(UHPLC-LTQ-Orbitrap-MS)对大鼠尾静脉注射热毒宁后血浆、胆汁、尿液和粪便进行分析,利用质量亏损过滤(MDF)技术进行京尼平苷、京尼平苷酸、断氧化马钱子苷、绿原酸代谢产物分析鉴定,推测出大鼠体内京尼平苷氧化、脱水、去甲氧基、水解、开环、半胱氨酸结合和苷元葡萄糖醛酸结合等14个代谢产物;京尼平苷酸脱水、开环、双键还原和半胱氨酸结合等9个代谢产物;断氧化马钱子苷水解、去甲氧基、羟基化和乙基化等6个代谢产物;绿原酸脱羧、水解、甲基化、乙酰化、半胱氨酰甘氨酸结合和谷胱甘肽结合等12个代谢产物。为进一步探讨热毒宁注射液体内过程,阐明其功效物质基础提供依据。

     

    Abstract: This study was designed to determine the metabolites of Renduining injection in rats. The ultra-high performance liquid chromatography-LTQ Orbitrap mass spectrometric (UHPLC-LTQ-Orbitrap-MS) and mass defect filter techniques were applied to analyze the metabolites of Reduning injection in rat plasma, bile, urine and feces. As a result, we determined 14 metabolites of geniposide, including oxidation, dehydration, hydroxymethylene loss, hydrolysis, ring-opened, cysteine conjugation and glucuronidation conjugation of aglycone; 9 metabolites of geniposidic acid, consisting of dehydration, ring-opened, double-bond reduction and cysteine conjugation; 6 metabolites of secoxylogain including hydrolysis, hydroxymethylene loss, hydroxylation and ethylation; 12 metabolites of chlorogenic acid, containing decarboxylation, hydrolysis, methylation, acetylation, cysteinylglycine conjugation and glutathione conjugation. It provided information for the therapeutic effect of Reduning in vivo.

     

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