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Identification of Metabolites of Eupatorin in Vivo and in Vitro Based on UHPLC-Q-TOF-MS/MS

机译:基于UHPLC-Q-TOF-MS / MS鉴定紫杉醇的体内和体外代谢物

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摘要

Eupatorin is the major bioactive component of Java tea (Orthosiphon stamineus), exhibiting strong anticancer and anti-inflammatory activities. However, no research on the metabolism of eupatorin has been reported to date. In the present study, ultra-high-performance liquid chromatography coupled with hybrid triple quadrupole time-of-flight mass spectrometry (UHPLC-Q-TOF-MS) combined with an efficient online data acquisition and a multiple data processing method were developed for metabolite identification in vivo (rat plasma, bile, urine and feces) and in vitro (rat liver microsomes and intestinal flora). A total of 51 metabolites in vivo, 60 metabolites in vitro were structurally characterized. The loss of CH2, CH2O, O, CO, oxidation, methylation, glucuronidation, sulfate conjugation, N-acetylation, hydrogenation, ketone formation, glycine conjugation, glutamine conjugation and glucose conjugation were the main metabolic pathways of eupatorin. This was the first identification of metabolites of eupatorin in vivo and in vitro and it will provide reference and valuable evidence for further development of new pharmaceuticals and pharmacological mechanisms.
机译:紫杉醇是爪哇茶(Orthosiphon stamineus)的主要生物活性成分,具有很强的抗癌和抗炎活性。然而,迄今尚未报道关于紫杉醇的代谢的研究。在本研究中,开发了结合高效三重四极杆飞行时间质谱(UHPLC-Q-TOF-MS)的超高效液相色谱与高效的在线数据采集和多种数据处理方法,用于代谢物体内(大鼠血浆,胆汁,尿液和粪便)和体外(大鼠肝微粒体和肠道菌群)的鉴定。体内共有51种代谢产物,体外有60种代谢产物的结构特征。 CH2,CH2O,O,CO的损失,氧化,甲基化,葡萄糖醛酸化,硫酸盐结合,N-乙酰化,氢化,酮形成,甘氨酸结合,谷氨酰胺结合和葡萄糖结合是紫杉醇的主要代谢途径。这是体内和体外对紫杉醇代谢产物的首次鉴定,它将为进一步开发新药物和药理机制提供参考和有价值的证据。

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