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作 者:居文政[1,2] 储继红[1] 谭仁祥[2] 熊宁宁[1]
机构地区:[1]南京中医药大学附属医院临床药理科,江苏-安徽中西药临床药代动力学联合实验室 [2]南京大学生命科学院
出 处:《中国临床药理学与治疗学》2006年第3期292-295,共4页Chinese Journal of Clinical Pharmacology and Therapeutics
基 金:科技部"临床试验关键技术及平台研究"课题资助(№2004AA2Z3766)
摘 要:目的:研究灯盏花乙素在胃肠道的代谢物。方法:分别用盐酸、β-葡糖醛酸苷酶水解灯盏花乙素,并用健康志愿者的肠内菌对灯盏花乙素进行转化,用超高效液相-串联质谱联用法分析代谢物。结果:灯盏花乙素可被盐酸、β-葡糖醛酸苷酶水解为苷元,可被肠内菌群转化为苷元。健康受试者口服灯盏花乙素后,血浆中能检测到灯盏花乙素苷元。结论:健康受试者口服灯盏花乙素后,在吸收进入血液之前,胃肠道内灯盏花乙素与其苷元并存,而苷元更易于吸收,以总苷元为检测对象研究灯盏花乙素药代动力学是合理的。AIM: The metabolites of scutellarin were studied in gastrointestinal tract. METHODS: Scutellarin was hydrolyzed with hydrochloric acid and β-glucuronidase. Human intestinal flora and scutellarin were incubated in vitro. The metabolites were identified by UPLC-MS/ MS method. RESULTS: Scutellarin could be hydrolyzed with hydrochloric acid and β-glucuronidase, and could be metabolized by human intestinal bacteria. A main metabolite, scutellarein, also was found in the plasma of healthy volunteers after oral administration. CONCLUSION: There were scutellarin and scutellarein in intestinal before absorption. It was suitable for scutellarin pharmacokinetic studies to determine scuteilarein or total aglycone.
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