Literature DB >> 16986209

Quantitative analyses of indoloquinazoline alkaloids in Fructus Evodiae by high-performance liquid chromatography with atmospheric pressure chemical ionization tandem mass spectrometry.

Yan Zhou1, Sheng-Hong Li, Ren-Wang Jiang, Min Cai, Xin Liu, Li-Sheng Ding, Hong-Xi Xu, Paul Pui-Hay But, Pang-Chui Shaw.   

Abstract

Fructus Evodiae (Wuzhuyu), the fruits of Evodia rutaecarpa and related varieties, is widely used in traditional Chinese medicine. The bioactive constituents include the indoloquinazoline alkaloids rutaecarpine, evodiamine and dehydroevodiamine. A new assay based on high-performance liquid chromatography/atmospheric pressure chemical ionization tandem mass spectrometry (HPLC/UV/APCI-MS/MS) was developed for the measurement of the indoloquinazoline alkaloids in commercial Fructus Evodiae products. Initially, the MS/MS fragmentation pathways of indoloquinazoline alkaloids were investigated to identify fragment ions that might be useful for the sensitive and selective detection of trace indoloquinazoline alkaloids during LC/MS/MS. Then, quantitative MS analysis of five indoloquinazoline alkaloids in 12 commercial Fructus Evodiae products from different geographical sources was performed. Analyte recovery was in the range of 97.5-105.3% for all with relative standard deviations (RSDs) below 6%, the intra-assay and inter-assay RSDs were less than 7%, and good linear relationships were shown with correlation coefficients for the analytes exceeding 0.999. Therefore, this LC/MS/MS assay facilitated the rapid quantitative analysis of rutaecarpine, evodiamine, evodiamide, 14-formyldihydrorutaecarpine and dehydroevodiamine in 12 commercial Fructus Evodiae products with excellent recovery, repeatability, accuracy and sensitivity. This method is simple and specific and can be used for identification and quality control of this traditional Chinese remedy. Copyright 2006 John Wiley & Sons, Ltd.

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Year:  2006        PMID: 16986209     DOI: 10.1002/rcm.2705

Source DB:  PubMed          Journal:  Rapid Commun Mass Spectrom        ISSN: 0951-4198            Impact factor:   2.419


  6 in total

1.  Evodiamide.

Authors:  Fang Cai; Jie Wu; Hai-Yan Tian; Xiao-Feng Yuan; Ren-Wang Jiang
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-01-07

2.  A study of the geo-herbalism of evodiae fructus based on a flow-injection mass spectrometric fingerprinting method combined with chemometrics.

Authors:  Yang Zhao; Xin Zhou; Yun-Ling Zhao; Xiao-Jian Gong; Chao Zhao
Journal:  Molecules       Date:  2015-02-03       Impact factor: 4.411

3.  Simultaneous Quantification of Limonin, Two Indolequinazoline Alkaloids, and Four Quinolone Alkaloids in Evodia rutaecarpa (Juss.) Benth by HPLC-DAD Method.

Authors:  Pei-Ting Zhang; Bi-Yan Pan; Qiong-Feng Liao; Mei-Cun Yao; Xin-Jun Xu; Jin-Zhi Wan; Dan Liu; Zhi-Yong Xie
Journal:  J Anal Methods Chem       Date:  2013-05-08       Impact factor: 2.193

4.  Development and validation of an UPLC-ESI-MS/MS method for determination of dehydroevodiamine, limonin, evodiamine, and rutaecarpine in Evodiae Fructus.

Authors:  Yang Zhao; Yunling Zhao; Xin Zhou; Xiaojian Gong
Journal:  Pharmacogn Mag       Date:  2014-07       Impact factor: 1.085

5.  Analysis of E. rutaecarpa Alkaloids Constituents In Vitro and In Vivo by UPLC-Q-TOF-MS Combined with Diagnostic Fragment.

Authors:  Shenshen Yang; Meng Tian; Lei Yuan; Haoyue Deng; Lei Wang; Aizhu Li; Zhiguo Hou; Yubo Li; Yanjun Zhang
Journal:  J Anal Methods Chem       Date:  2016-06-30       Impact factor: 2.193

6.  Evodiamine stabilizes topoisomerase I-DNA cleavable complex to inhibit topoisomerase I activity.

Authors:  Agnes L-F Chan; Wen-Shin Chang; Li-Min Chen; Chi-Ming Lee; Chiao-En Chen; Chun-Mao Lin; Jau-Lang Hwang
Journal:  Molecules       Date:  2009-03-27       Impact factor: 4.411

  6 in total

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