Investigation of the hydrolysis of ginsenosides by high performance liquid chromatography-electrospray ionization mass spectrometry

被引:23
作者
Zhan, Xu
Song, Fengrui
Cui, Meng
Liu, Zhiqiang
Liu, Shuying [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, Changchun Ctr Mass Spectrometry, Changchun 130022, Peoples R China
[2] Grad Univ, Chinese Acad Sci, Beijing, Peoples R China
关键词
hydrolysis; ginseng; Panax ginseng; Panax quinquefolius; Araliaceae; ginsenoside; HPLC-ESI-MS;
D O I
10.1055/s-2007-981590
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
The hydrolysis of ginsenoside standards and the crude extracts of ginseng has been investigated at different pH values (2.4 - 11.2) using high performance liquid chromatography-electrospray ionization mass spectrometry (HPLC-ESI-MS). The experimental results indicated that the pH value of aqueous solutions is an important factor in changing the composition of ginsenosides. For (20S)-protopanaxadiol ginsenosides, ginsenosides with a large mass hydrolyzed to form hydrolysates (20S)-Rg(3) and (20R)-Rg(3) at pH 4.3. There were more hydrolyzed products observed at pH 3.3: (20S)-F-2, C-25,26 hydrated ginsenoside "C-Y-1" and "C-Y-2" (MW = 802 Da) accompanied with (20S)-Rg(3), (20R)-Rg(3). At pH 2.4, only (20R)-Rg(3), (20S)-F-2, a small quantity of (20S)-Rg(3) and three C-25,26 hydrated ginsenosides were obtained. For (20S)protopanaxatriol Re, no hydrolysates were observed at pH 4.3; it was hydrolyzed at pH 3.3 to form hydrolysates (20S)-Rg, (20R)Rg(2) and hydrated C-25,26 (MW = 802 Da) and at pH 2.4 only C-25,26 hydrated ginsenosides "C-Y-1" and "C-Y-2" (MW = 802 Da) were left in the solution. Similar hydrolysis reactions could be also observed for the crude extracts of ginseng. It showed that HPLC/ESI-MS is a fast and convenient method to study the hydrolysis of ginseng.
引用
收藏
页码:1225 / 1229
页数:5
相关论文
共 23 条
[1]
Ginseng pharmacology - Multiple constituents and multiple actions [J].
Attele, AS ;
Wu, JA ;
Yuan, CS .
BIOCHEMICAL PHARMACOLOGY, 1999, 58 (11) :1685-1693
[2]
Transformation of ginseng saponins to ginsenoside Rh2 by acids and human intestinal bacteria and biological activities of their transformants [J].
Bae, EA ;
Han, MJ ;
Kim, EJ ;
Kim, DH .
ARCHIVES OF PHARMACAL RESEARCH, 2004, 27 (01) :61-67
[3]
Liquid chromatography-electrospray ionization mass spectrometry for metabolism and pharmacokinetic studies of ginsenoside Rg3 [J].
Cai, ZW ;
Qian, TX ;
Wong, RNS ;
Jiang, ZH .
ANALYTICA CHIMICA ACTA, 2003, 492 (1-2) :283-293
[4]
Determination of marker constituents in radix Glycyrrhizae and radix Notoginseng by near infrared spectroscopy [J].
Chen, YX ;
Sorensen, LK .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 2000, 367 (05) :491-496
[5]
A COMPARATIVE-STUDY ON COMMERCIAL SAMPLES OF GINSENG-RADIX [J].
CHUANG, WC ;
WU, HK ;
SHEU, SJ ;
CHIOU, SH ;
CHANG, HC ;
CHEN, YP .
PLANTA MEDICA, 1995, 61 (05) :459-465
[6]
DETERMINATION OF GINSENOSIDES IN GINSENG CRUDE EXTRACTS BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
CHUANG, WC ;
SHEU, SJ .
JOURNAL OF CHROMATOGRAPHY A, 1994, 685 (02) :243-251
[7]
Quantitative determination of ginsenosides from Panax ginseng roots and ginseng preparations by thin layer chromatography-densitometry [J].
Corthout, J ;
Naessens, T ;
Apers, S ;
Vlietinck, AJ .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1999, 21 (01) :187-192
[8]
IDENTIFICATION AND QUANTIFICATION OF GINSENOSIDES IN VARIOUS COMMERCIAL GINSENG PREPARATIONS [J].
CUI, JF .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 3 (02) :77-85
[9]
Cui M, 2000, RAPID COMMUN MASS SP, V14, P1280, DOI 10.1002/1097-0231(20000730)14:14<1280::AID-RCM26>3.0.CO
[10]
2-C