Affiliated Hospital on Integration of Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, 210023, China; Key Laboratory of New Drug Delivery System of Chinese Meteria Medica, Jiangsu Provincial Academy of Chinese Medicine, 100 Shizi Road, Nanjing, Jiangsu 210028, China.
Affiliated Hospital on Integration of Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, 210023, China; Key Laboratory of New Drug Delivery System of Chinese Meteria Medica, Jiangsu Provincial Academy of Chinese Medicine, 100 Shizi Road, Nanjing, Jiangsu 210028, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Apr 1;955-956:20-5. doi: 10.1016/j.jchromb.2014.02.010. Epub 2014 Feb 19.
In our research, ultraperformance liquid chromatography/quadrupole-time-of-flight mass spectrometry (U-HPLC/Q-TOF-MS) was established for analyzing the metabolite profiles of Danshensu (DSS) in rat feces, bile, urine, plasma and the possible metabolic pathways were subsequently proposed after the oral dose of 80mg/kg; rat biological samples were collected and pretreated by protein precipitation. Then, the samples were injected into an Acquity ultraperformance liquid chromatography BEHC column with mobile phase consisted of acetonitrile (solvent A)-0.1% formic acid-water (solvent B) with a linear gradient elution program. Totally, 17 metabolites of DSS were identified, including 4, 5, 4 and 4 metabolites in the feces, urine, blood, and bile samples respectively. Most of them were to our knowledge reported for the first time. The results indicated that DSS was metabolized via dehydrogenation, deoxygenation, methylation, glucuronidation, and sulfation pathways in vivo. Among these, methylation was considered as the main physiologic processes of it. This study revealed that U-HPLC/Q-TOF-MS was more accurate and sensitive to detect and identify the possible metabolites and to better understand the metabolism of DSS in vivo.
在我们的研究中,建立了超高效液相色谱/四极杆飞行时间质谱(U-HPLC/Q-TOF-MS)来分析丹酚酸(DSS)在大鼠粪便、胆汁、尿液、血浆中的代谢物谱,随后在口服 80mg/kg 后提出了可能的代谢途径;收集大鼠生物样本并通过蛋白质沉淀进行预处理。然后,将样品注入 Acquity 超高效液相色谱 BEHC 柱,流动相由乙腈(溶剂 A)-0.1%甲酸-水(溶剂 B)组成,采用线性梯度洗脱程序。总共鉴定出 17 种 DSS 代谢物,包括粪便、尿液、血液和胆汁样本中分别有 4、5、4 和 4 种代谢物。其中大多数是我们首次报道的。结果表明,DSS 在体内通过脱氢、脱氧、甲基化、葡萄糖醛酸化和硫酸化途径代谢。其中,甲基化被认为是其主要的生理过程。本研究表明,U-HPLC/Q-TOF-MS 更准确、更灵敏地检测和鉴定可能的代谢物,并更好地了解 DSS 在体内的代谢。