首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >An untargeted metabolomics-driven approach based on LC-TOF/MS and LC-MS/MS for the screening of xenobiotics and metabolites of Zhi-Zi-Da-Huang decoction in rat plasma
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An untargeted metabolomics-driven approach based on LC-TOF/MS and LC-MS/MS for the screening of xenobiotics and metabolites of Zhi-Zi-Da-Huang decoction in rat plasma

机译:基于LC-TOF / MS和LC-MS / MS的非靶向代谢组学驱动方法在大鼠血浆中筛选智芝大黄汤的异种生物和代谢物

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摘要

Zhi-Zi-Da-Huang decoction (ZZDHD), a typical traditional Chinese medicine prescription, is widely used in clinical practice for the treatment of alcoholic liver disease. However, due to lack of holistic metabolic research, the active ingredients of ZZDHD have not been fully elucidated. It entails a huge obstacle for the quality evaluation, pharmacokinetic studies and clinical-safe medication administration of ZZDHD. In this work, an untargeted metabolomics-driven approach was proposed to rapidly screen and characterize xenobiotics and related metabolites in vivo conducted by LC-TOF/MS and LC-QqQ/MS. The t(R)-m/z pairs which were present in the ZZDHD-dosed group and absent in the control group could be clearly displayed by XCMS Online platform combined with supervised orthogonal partial least squares discriminant analysis. Among them, a total of 61 ZZDHD-related xenobiotics and metabolites including 34 prototype components and 27 metabolites were rapidly identified or tentatively characterized in rat plasma. The results indicated that iridoid glycosides and monoterpenoids from Gardenia jasminoides Ellis, flavonoid glycosides from Citrus aurantium L, as well as anthraquinones from Rheum palmatum L. were the main absorbed chemical components of ZZDHD. Hydrolysis, glucuronidation and sulfation were the main metabolic pathways of ZZDHD in vivo. The present study provided a solid basis for further revealing the relationship between the xenobiotic metabolome and pharmacological activity of ZZDHD. In addition, the application of untargeted metabolomics-driven approach offers a fresh insight for rapid screening and identifying xenobiotics and metabolites of ZZDHD and other multiherb prescription. (C) 2015 Elsevier B.V. All rights reserved.
机译:芝子大黄汤(ZZDHD)是一种典型的中药处方,在临床上广泛用于治疗酒精性肝病。但是,由于缺乏整体代谢研究,ZZDHD的活性成分尚未得到充分阐明。 ZZDHD的质量评估,药代动力学研究和临床安全用药管理面临巨大障碍。在这项工作中,提出了一种无目标代谢组学驱动的方法,以通过LC-TOF / MS和LC-QqQ / MS在体内快速筛选和表征异种生物及相关代谢物。 XCMS Online平台结合监督的正交偏最小二乘判别分析可以清楚地显示ZZDHD剂量组中存在的t(R)-m / z对,对照组中不存在。其中,在大鼠血浆中迅速鉴定或初步鉴定了总共61种与ZZDHD相关的异种生物和代谢物,包括34种原型成分和27种代谢物。结果表明,茉莉ia子中的鸢尾苷和单萜类化合物,桔皮中的黄酮苷以及大黄中的蒽醌类是ZZDHD的主要吸收化学成分。水解,葡萄糖醛酸化和硫酸化是ZZDHD在体内的主要代谢途径。本研究为进一步揭示异源代谢组与ZZDHD药理活性之间的关系提供了坚实的基础。此外,无目标代谢组学驱动方法的应用为快速筛选和鉴定ZZDHD和其他多药处方的异种生物和代谢物提供了新的见识。 (C)2015 Elsevier B.V.保留所有权利。

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