Determination of aconitine-type alkaloids as markers in fuzi (Aconitum carmichaeli) by LC/(+)ESI/MS3

被引:68
作者
Chen, Jung-Hui [1 ]
Lee, Cheng-Yu [1 ]
Liau, Bing-Chung [1 ]
Lee, Maw-Rong [1 ]
Jong, Ting-Ting [1 ]
Chiang, Shu-Tuan [2 ]
机构
[1] Natl Chung Hsing Univ, Dept Chem, Taichung 40227, Taiwan
[2] Chuang Song Zong Pharmaceut Co Ltd, Ligang Shiang, Pingtung, Taiwan
关键词
Aconitine; Mesaconitine; Hypaconitine; Aconitum carmichaeli; Fuzi;
D O I
10.1016/j.jpba.2008.08.022
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
LC/(+)ESI/MS3 was used to determine aconitine, mesaconitine, and hypaconitine as target markers in crude methanol extracts of (i) the raw lateral roots of Aconitum carmichaeli, (ii) roots treated by three different refining processes, and (iii) eight generally available traditional Chinese medicine (TCM) preparations containing fuzi (treated lateral roots of A. carmichaeli). The optimal ionization behavior resulted when using electrospray ionization (ESI) in positive-ion mode with 0.005% TFA as an additive in the mobile phase. The consecutive reaction monitoring(CRM) mode provided additional improvements in selectivity, which was exploited to minimize the noise and interference problems. Employing this approach, aconitine and mesaconitine were found to decompose readily during the refining processes, but hypaconitine remains present at the same content, presumably because of its characteristic chemical Structure. Thus, treated and untreated fuzi samples can be distinguished by monitoring the ratio of aconitine and mesaconitine to hypaconitine. The limits of detection (LODs) for these three markers were 0.05, 0.08, and 0.03 ng/ml. The linearity range for the three marker compounds was 0.1-1000 ng/ml. The analysis time was 12 min per sample. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1105 / 1111
页数:7
相关论文
共 13 条
  • [1] CHAN TYK, 1994, VET HUM TOXICOL, V36, P452
  • [2] Report on the preparation of deuterium-labelled aconitine and mesaconitine and their application to the analysis of these alkaloids from body fluids as internal standard
    Ito, K
    Tanaka, S
    Konno, S
    Konishi, Y
    Mizugaki, M
    [J]. JOURNAL OF CHROMATOGRAPHY B, 1998, 714 (02): : 197 - 203
  • [3] Ma HY, 2006, LISHIZHEN MED MAT ME, V17, P208
  • [4] Determination of Aconitum alkaloids in blood and urine samples .1. High-performance liquid chromatographic separation, solid-phase extraction and mass spectrometric confirmation
    Ohta, H
    Seto, Y
    Tsunoda, N
    [J]. JOURNAL OF CHROMATOGRAPHY B, 1997, 691 (02): : 351 - 356
  • [5] PAN ZA, 2005, PHARMACOPOEIA CHINA, P132
  • [6] PHARMACOLOGICAL ACTIONS OF ACONITINE ALKALOIDS
    SATO, H
    YAMADA, C
    KONNO, C
    OHIZUMI, Y
    ENDO, K
    HIKINO, H
    [J]. TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, 1979, 128 (02) : 175 - 187
  • [7] Sun WX, 1998, RAPID COMMUN MASS SP, V12, P821, DOI 10.1002/(SICI)1097-0231(19980715)12:13<821::AID-RCM242>3.0.CO
  • [8] 2-Z
  • [9] Electrospray ionization tandem mass spectrometric study of the aconitines in the roots of aconite
    Wang, Y
    Liu, ZQ
    Song, FR
    Liu, SY
    [J]. RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2002, 16 (22) : 2075 - 2082
  • [10] Quantitative determination of diterpenoid alkaloids in four species of Aconitum by HPLC
    Wang, ZH
    Wen, J
    Xing, JB
    He, Y
    [J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2006, 40 (04) : 1031 - 1034