Rapid profiling and identification of triterpenoid saponins in crude extracts from Albizia julibrissin Durazz. by ultra high-performance liquid chromatography coupled with electrospray ionization quadrupole time-of-flight tandem mass spectrometry

被引:43
作者
Han, Lifeng [1 ]
Pan, Guixiang [1 ]
Wang, Yuefei [1 ]
Song, Xinbo [1 ]
Gao, Xiumei [1 ]
Ma, Baiping [2 ]
Kang, Liping [1 ,2 ]
机构
[1] Tianjin Univ Tradit Chinese Med, Tianjin State Key Lab Modern Chinese Med, Tianjin 300193, Peoples R China
[2] Beijing Inst Radiat Med, Beijing 100850, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
Albizia julibrissin Durazz; UHPLC/ESI-Q-TOF; Triterpenoid saponins; Identification; ALBIZZIAE CORTEX; DIASTEREOISOMERIC SAPONINS; CYTOTOXIC SAPONIN; LEGUMINOUS PLANTS; GLYCOSIDES; PATHWAY;
D O I
10.1016/j.jpba.2011.04.002
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Ultra high-performance liquid chromatography coupled with electrospray ionization quadrupole time-of-flight tandem mass spectrometry (UHPLC/ESI-Q-TOF-MS/MS) was applied to separate and identify triterpenoid saponins in crude extract from the stem bark of Albizia julibrissin Durazz. The molecular weights were determined by comparing quasi-molecular ions [M+NH4](+) in positive mode and [M-H](-) and [M-2H](2-) ions in negative mode. The MS/MS spectra of the [M-H](-) ions for saponins provided a wealth of structural information related to aglycone skeletons, sugar types and linked sequence. On the basis of the fragmentation behavior of known saponins isolated before, saponins from this plant were identified, even though references were not available. As a result, a total of twenty-eight saponins in the crude extract were identified, which all had a common basic skeleton of the triterpene oleanolic acid and eight of them were new compounds. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:994 / 1009
页数:16
相关论文
共 32 条
[1]   1H and 13C NMR assignments for four triterpenoid saponins from Albizziae cortex [J].
Han, Li-Feng ;
Ma, Bai-Ping ;
Zhang, Hong-Sheng ;
Song, Xin-Bo ;
Gao, Xiu-Mei ;
Kang, Li-Ping ;
Xiong, Cheng-Qi ;
Zhao, Yang ;
Tan, Da-Wei .
MAGNETIC RESONANCE IN CHEMISTRY, 2008, 46 (11) :1059-1065
[2]  
HIGUCHI H, 1992, CHEM PHARM BULL, V40, P829, DOI 10.1248/cpb.40.829
[3]   STUDIES ON LEGUMINOUS PLANTS .29. 4 NEW GLYCOSIDES FROM ALBIZZIAE CORTEX .3. [J].
HIGUCHI, H ;
FUKUI, K ;
KINJO, J ;
NOHARA, T .
CHEMICAL & PHARMACEUTICAL BULLETIN, 1992, 40 (02) :534-535
[4]   Cytotoxic glycosides from Albizia julibrissin [J].
Ikeda, T ;
Fujiwara, S ;
Araki, K ;
Kinjo, J ;
Nohara, T ;
Miyoski, T .
JOURNAL OF NATURAL PRODUCTS, 1997, 60 (02) :102-107
[5]   IDENTIFICATION OF FLAVONES IN 16 LEGUMINOSAE SPECIES [J].
KANETA, M ;
HIKICHI, H ;
ENDO, S ;
SUGIYAMA, N .
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1980, 44 (06) :1407-1408
[6]  
KINJO J, 1991, CHEM PHARM BULL, V39, P2952, DOI 10.1248/cpb.39.2952
[7]   6 NEW TRITERPENOIDAL GLYCOSIDES INCLUDING 2 NEW SAPOGENOLS FROM ALBIZZIAE CORTEX .5. [J].
KINJO, J ;
ARAKI, K ;
FUKUI, K ;
HIGUCHI, H ;
IKEDA, T ;
NOHARA, T ;
IDA, Y ;
TAKEMOTO, N ;
MIYAKOSHI, M ;
SHOJI, J .
CHEMICAL & PHARMACEUTICAL BULLETIN, 1992, 40 (12) :3269-3273
[8]  
KINJO J, 1991, CHEM PHARM BULL, V39, P1623, DOI 10.1248/cpb.39.1623
[9]   An antitumor compound julibroside J28 from Albizia julibrissin [J].
Liang, H ;
Tong, WY ;
Zhao, YY ;
Cui, JR ;
Tu, GZ .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2005, 15 (20) :4493-4495
[10]   NMR determination of the structure of Julibroside J(1) [J].
Ma, LB ;
Tu, GZ ;
Chen, SP ;
Zhang, RY ;
Lai, LH ;
Xu, XJ ;
Tang, YQ .
CARBOHYDRATE RESEARCH, 1996, 281 (01) :35-46