Literature DB >> 28284081

An integrated strategy using UPLC-QTOF-MSE and UPLC-QTOF-MRM (enhanced target) for pharmacokinetics study of wine processed Schisandra Chinensis fructus in rats.

Kuangyi Liu1, Yonggui Song1, Yali Liu1, Mi Peng1, Hanyun Li1, Xueliang Li1, Bingwei Feng1, Pengfei Xu1, Dan Su2.   

Abstract

Currently the pharmacokinetic (PK) research of herbal medicines is still limited and facing critical technical challenges on quantitative analysis of multi-components from biological matrices which often accompanied by lacking of authentic standards and low concentration. This present work contributes to the development of an integrated strategy for extensive pharmacokinetics assessments, and a selective and sensitive method independent of authentic standards for multi-components analysis based on the use of ultra-performance liquid chromatography/quadrupole-time-of-flight/MSE (UPLC-TOF-MSE) and UPLC-TOF-MRM (rnhanced target). Initially, phytochemicals were identified by UPLC-TOF-MSE analysis, subsequently the identified components were matched with authentic standards and pre-classified, and UPLC-QTOF-MRM method optimized and developed. To guarantee reliable results, three rules are necessary: (1) detection with a mass error of less than 5ppm; (2) same class chemical compositions with structural high similarity between analytes with and without authentic reference substance; (3) a matching retention time between TOF-MRM mode and TOF-MSE within 0.2min. The developed and validated method was applied for the simultaneous determination of 12 lignans in rat plasma after administered with wine processed Schisandra Chinensis fructus (WPSCF) extract. Such an approach was found capable of providing extensive pharmacokinetic profiles of multi-components absorbed into blood after oral administrated with WPSCF extract. The results also indicated that significant difference in pharmacokinetics parameters of dibenzocyclooctadiene lignans was observed between schizandrin and gomisin compounds. For lignans, the absorption via gastrointestinal tract were all rapid and maintained relatively long retention time, especially for schisantherin A and schisantherin B with higher plasma exposure.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Herbal medicine; Pharmacokinetics; QTOF-MRM; QTOF-MS(E); Wine processed Schisandra Chinensis fructus

Mesh:

Substances:

Year:  2017        PMID: 28284081     DOI: 10.1016/j.jpba.2017.02.043

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  7 in total

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Review 2.  A Comprehensive Review of the Main Lignan Components of Schisandra chinensis (North Wu Wei Zi) and Schisandra sphenanthera (South Wu Wei Zi) and the Lignan-Induced Drug-Drug Interactions Based on the Inhibition of Cytochrome P450 and P-Glycoprotein Activities.

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6.  The Anti-colitis Effect of Schisandra chinensis Polysaccharide Is Associated With the Regulation of the Composition and Metabolism of Gut Microbiota.

Authors:  Lianlin Su; Chunqin Mao; Xiachang Wang; Lin Li; Huangjin Tong; Jing Mao; Tulin Lu; Min Hao; Ziyan Huang; Chenghao Fei; Kewei Zhang; Guojun Yan
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7.  Obese rats intervened with Rhizoma coptidis revealed differential gene expression and microbiota by serum metabolomics.

Authors:  Yanhua Ji; Kexin Luo; Jiri Mutu Zhang; Peng Ni; Wangping Xiong; Xiaoquan Luo; Guoliang Xu; Hongning Liu; Zhijun Zeng
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  7 in total

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