Study of the determination and pharmacokinetics of Compound Danshen Dripping Pills in human serum by column switching liquid chromatography electrospray ion trap mass spectrometry

被引:50
作者
Pei, WJ
Zhao, XF
Zhu, ZM
Lin, CZ
Zhao, WM
Zheng, XH
机构
[1] Xian Jiaotong Univ, Sch Med, Engn & Res Ctr, Chinese Herb Modernizat, Xian 710061, Peoples R China
[2] Xian Jiaotong Univ, Sch Life Sci & Technol, Dept Biol Engn, Xian, Peoples R China
[3] Xian Jiaotong Univ, Sch Sci, Xian, Peoples R China
[4] Xian Jiaotong Univ, Dept Pharm, Hosp 2, Xian, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2004年 / 809卷 / 02期
关键词
Compound Danshen Dripping Pill;
D O I
10.1016/j.jchromb.2004.06.028
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Compound Danshen Dripping Pill (CDDP) is an important drug widely used for the treatment of cardiovascular diseases. An active component Danshensu (DS) of CDDP was separated by reversed-phase high performance liquid chromatography using column-switching system and analyzed by electrospray mass spectrometry. With this validated assay the pharmacokinetics of CDDP was studied in 10 healthy volunteers after a single oral administration of 250 mg. After trichloroacetic acid precipitation of serum proteins, the analytes were preconcentrated and black-flushed on a reversed-phase column for separation using a switching valve. The analytes were ionized using negative electrospray ionization (ESI) mode. The precursor ion of m/z 196.6 was used to quantify DS in serum. The linear calibration curve ranged from 1.25 to 175mug/mL. The limit of quantification (LOQ) for DS was 0.15mug/mL. The intra-day and inter-day precision (R.S.D.) was less than 7.4 and 7.9%, respectively. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:237 / 242
页数:6
相关论文
共 22 条
[1]  
Bai Y, 2004, CHEM J CHINESE U, V25, P284
[2]  
DENG CE, 2003, LISHIZHEN MED MAT ME, V14, P776
[3]   Column switching in high-performance liquid chromatography with tandem mass spectrometric detection for high-throughput preclinical pharmacokinetic studies [J].
Gao, VCX ;
Luo, WC ;
Ye, QP ;
Thoolen, M .
JOURNAL OF CHROMATOGRAPHY A, 1998, 828 (1-2) :141-148
[4]   Magnesium tanshinoate B (MTB) inhibits low density lipoprotein oxidation [J].
Karmin, O ;
Lynn, EG ;
Vazhappilly, R ;
Au-Yeung, KKW ;
Zhu, DY ;
Siow, YL .
LIFE SCIENCES, 2001, 68 (08) :903-912
[5]  
Kyoko T, 2002, BIOCHEM PHARMACOL, V64, P745
[6]   Preparative isolation and purification of salvianolic acid B from the Chinese medicinal plant Salvia miltiorrhiza by high-speed counter-current chromatography [J].
Li, HB ;
Lai, JP ;
Jiang, Y ;
Chen, F .
JOURNAL OF CHROMATOGRAPHY A, 2002, 943 (02) :235-239
[7]   Preparative isolation and purification of six diterpenoids from the Chinese medicinal plant Salvia miltiorrhiza by high-speed counter-current chromatography [J].
Li, HB ;
Chen, F .
JOURNAL OF CHROMATOGRAPHY A, 2001, 925 (1-2) :109-114
[8]  
Li Zhi-qun, 2004, Zhonghua Gan Zang Bing Za Zhi, V12, P378
[9]   Determination of Danshensu, a major active compound of Radix Salvia miltiorrhiza in dog plasma by HPLC with fluorescence detection [J].
Luo, XJ ;
Bi, KS ;
Zhou, SY ;
Wei, QH ;
Zhang, RH .
BIOMEDICAL CHROMATOGRAPHY, 2001, 15 (08) :493-496
[10]  
MA X, 2003, J CHROMATOGR, V21, P562