Abstract
Guan Xin II decoction (GX II) is a widely used traditional Chinese medicine (TCM)
formula for the treatment of coronary heart diseases. However, the comprehensive chemical
analysis of the formulated GX II is not clarified yet. An HPLC-DAD-ESI-MSn method was established to analyze GX II and its five component herbs, respectively.
A total of 57 compounds, including phenolic acids, glycosides, flavonoids, and alkaloids
were identified or tentatively characterized on the basis of their mass spectra or
by comparison with reference standards. This is the first time that the chemical composition
of GX II was elucidated by LC/MS. The established method will be used for quality
control and pharmacokinetic studies of GX II.
Abbreviations
GX II:Guan Xin II, Guan Xin Er Hao (in Chinese)
TCM:traditional Chinese medicine
Key words
chemical analysis - Chinese medicine - Guan Xin II decoction - HPLC-DAD-ESI-MSn
References
- 1
Shen P A.
Proved recipes for treatment of coronary heart disease by traditional Chinese medicine.
World Clin Drugs.
2006;
4
229-32
- 2
Gan H Q, Huang X, Tian X Q.
Effect of oral administration of GuanXin II decoction on coronary blood flow and cardiac
systolic/diastolic function in healthy males.
Chin J Integr Tradit West Med.
2004;
24
785-9
- 3
Yang X G, Peng B, Zhang G H, Wei L L, Nie S F, Pan W S.
Studies of the pharmacokinetics of paeoniflorin in two Jing–Zhi–Guan–Xin formulations
after oral administration to beagle dogs.
J Pharm Biomed Anal.
2006;
41
320-4
- 4
Tang W F, Chen D Z, Huang X, Ren P, Xia Q, Wan M H. et al .
Effect of coronary heart NO2 on the hemodynamics of inferior mesentery artery in healthy
male volunteers.
Chin J Exp Tradit Med Formulae.
2006;
12
70-2
- 5
Liu A H, Guo H, Ye M, Lin Y H, Sun J H, Xu M. et al .
Detection, characterization and identification of phenolic acids in Danshen using
high-performance liquid chromatography with diode array detection and electrospray
ionization mass spectrometry.
J Chromatogr A.
2007;
1161
170-82
- 6
Teng J W, Chen H W, Li D L, Luo A D.
Identification and characterization of supercritical fluid extracts of Rhizoma Chuanxiong
by high performance liquid chromatography ion trap mass spectrometry.
Front Chem China.
2006;
4
454-8
- 7
Kong L, Yu Z Y, Bao Y M, Su X Y, Zou H F, Li X.
Screening and analysis of an antineoplastic compound in Rhizoma Chuanxiong by means
of in vitro metabolism and HPLC-MS.
Anal Bioanal Chem.
2006;
386
264-74
- 8
Wang Q, Liu R X, Guo H Z, Ye M, Huo C H, Bi K S. et al .
Simultaneous LC determination of major constituents in red and white peony root.
Chromatographia.
2005;
62
581-8
- 9
Xie G X, Qiu M F, Zhao A H, Jia W.
Fingerprint analysis of Flos Carthami by pressurized CEC and LC.
Chromatographia.
2006;
64
739-43
- 10
Liu R X, Ye M, Guo H Z, Bi K S, Guo D A.
Liquid chromatography/electrospray ionization mass spectrometry for the characterization
of twenty-three flavonoids in the extract of Dalbergia odorifera.
Rapid Commun Mass Spectrom.
2005;
19
1557-65
- 11
Yang M, Liu A H, Guan S H, Sun J H, Xu M, Guo D A.
Characterization of tanshinones in the roots of Salvia miltiorrhiza (Dan-shen) by high-performance liquid chromatography with electrospray ionization
tandemmass spectrometry.
Rapid Commun Mass Spectrom.
2006;
20
1266-80
- 12
Zhang J L, Cui M, He Y, Yu H L, Guo D A.
Chemical fingerprint and metabolic fingerprint analysis of Danshen injection by HPLC-UV
and HPLC-MS methods.
J Pharm Biomed Anal.
2005;
36
1029-35
- 13
Liu R X, Wang Q, Bi K S, Guo D A.
Chromatographic fingerprint of Dalbergia odorifera and its application in the identification of the crude drugs of different origins.
Acta Pharm Sin.
2005;
40
1008-12
- 14
Huang X, Song F R, Liu Z Q, Liu S Y.
Studies on lignan constituents from Schisandra chinensis (Turcz.) Baill. fruits using high-performance liquid chromatography/electrospray
ionization multiple-stage tandem mass spectrometry.
J Mass Spectrom.
2007;
42
1148-61
- 15
Ye M, Guo D A.
Analysis of bufadienolides in the Chinese drug ChanSu by high-performance liquid chromatography
with atmospheric pressure chemical ionization tandem mass spectrometry.
Rapid Commun Mass Spectrom.
2005;
19
1881-92
- 16
Yang L, Nakamura N, Hattori M, Wang Z T, Bligh A SW, Xu L S.
High-performance liquid chromatography-diode array detection/electrospray ionization
mass spectrometry for the simultaneous analysis of cis-, trans- and dihydro-2-glucosyloxycinnamic acid derivatives from Dendrobium medicinal plants.
Rapid Commun Mass Spectrom.
2007;
21
1833-40
- 17
Xu M, Guo H, Han J, Sun S F, Liu A H, Wang B R. et al .
Structural characterization of metabolites of salvianolic acid B from Salvia miltiorrhiza in normal and antibiotic-treated rats by liquid chromatography-mass spectrometry.
J Chromatogr B.
2007;
858
184-98
- 18
Ye G, Li Y Z, Li Y Y, Guo H Z, Guo D A.
SPE-HPLC method for the determination and pharmacokinetic studies on paeoniflorin
in rat serum after oral administration of traditional Chinese medicinal preparation
Guan-Xin-Er-Hao decoction.
J Pharm Biomed Anal.
2003;
33
521-7
- 19
Liu M, Li Y G, Chou G X, Cheng X M, Zhang M, Wang Z T.
Extraction and ultra-performance liquid chromatography of hydrophilic and lipophilic
bioactive components in a Chinese herb Radix Salviae Miltiorrhizae.
J Chromatogr A.
2007;
1157
51-5
- 20
Li G, Wang Q G, Wang Y M, Luo G A.
Study on chromatographic quantitative analysis of flavonoids.
Food Sci.
2001;
2
57-61
- 21
Li X C, Yu C, Wang L, Lu Y L, Wang W Y, Xuan L J. et al .
Simultaneous determination of lithospermic acid B and its three metabolites by liquid
chromatography/tandem mass spectrometry.
J Pharm Biomed Anal.
2007;
43
1864-8
- 22
Zeng G F, Xiao H B, Liu J X, Liang X M.
Identification of phenolic constituents in Radix Salvia miltiorrhizae by liquid chromatography/electrospray
ionization mass spectrometry.
Rapid Commun Mass Spectrom.
2006;
20
499-506
- 23
Lee J H, Johnson J V, Talcott S T.
Identification of ellagic acid conjugates and other polyphenolics in muscadine grapes
by HPLC-ESI-MS.
J Agric Food Chem.
2005;
53
6003-10
- 24
Lin H F, Wei L C, Tang C J.
Antihyperglycemic effects of paeoniflorin and 8-debenzoylpaeoniflorin, glucosides
from the root of Paeonia lactiflora.
.
Planta Med.
1997;
63
323-5
- 25
Nobutoshi M, Masami S, Hiromi S, Hisashi M, Johji Y, Masayuki Y.
New bioactive monoterpene glycosides from Paeoniae Radix.
Chem Pharm Bull.
1996;
44
1279-81
- 26
Kaneda M, Litaka Y, Shibata S.
Chemical studies on the oriental plant drugs. XXXIII. Absolute structure of paeoniflorin,
albiflorin, oxypaeoniflorin, and benzoylpaeoniflorin isolated from Chinese paeony
root.
Tetrahedron.
1972;
28
4309-17
- 27
Xu S J, Yang L, Zeng X, Zhang M, Wang Z T.
Characterization of compounds in the Chinese herbal drug Mu-Dan-Pi by liquid chromatography
coupled to electrospray ionization mass spectrometry.
Rapid Commun Mass Spectrom.
2006;
20
3275-88
- 28
Zhou Y, Wang M K, Liao X, Zhu X M, Peng S L, Ding H.
Rapid identification of compounds in Glycyrrhiza uralensis by liquid chromatography/tandem mass spectrometry.
Chin J Anal Chem.
2004;
32
174-8
- 29
Yang X P, Yuan C S, Jia Z J.
Chemical constituents from the roots of Patrinia rupestris.
.
J Chin Chem Soc.
2007;
54
459-63
- 30
Wanjala C CW, Majinda R RT.
A new isoflavanone from the stem bark of Erythrina latissima.
.
Fitoterapia.
2000;
71
400-5
- 31
Balakrishna S, Ramanathan J D, Seshadri T R, Venkataramani B.
Isoflavanones from Ougeinia dalbergioides.
.
J Sci Indian Res.
1961;
20
134-5
- 32
Hattori M, Huang X L, Che Q M, Kawata Y, Tezuka Y, Kikuchi T. et al .
6-Hydroxykaempferol and its glycosides from Carthamus tinctorius petals.
Phytochemistry.
1992;
31
4001-4
- 33
Iizuka T, Nagai M, Moriyama H, Taniguchi A, Hoshi K A.
Antiplatelet aggregatory effects of the constituents isolated from the flower of Carthamus tinctorius.
.
Nat Med.
2005;
59
241-4
Prof. Dr. De-an Guo
The State Key Laboratory of Natural and Biomimetic Drugs
School of Pharmaceutical Sciences
Peking University
38 Xueyuan Road
Beijing 100083
People’s Republic of China
Phone: +86-10-8280-1516
Fax: +86-10-8280-2700
Email: gda@bjmu.edu.cn