Chemical profiling of San-Huang decoction by UPLC-ESI-Q-TOF-MS

被引:28
|
作者
Liu, Qingfeng [1 ]
Jiao, Zheng [1 ]
Liu, Yi [2 ]
Li, Zhongdong [1 ]
Shi, Xiaojin [1 ]
Wang, Wenjian [2 ]
Wang, Bin [1 ]
Zhong, Mingkang [1 ]
机构
[1] Fudan Univ, Huashan Hosp, Clin Pharm Lab, 12 Wu Lu Mu Qi M Rd, Shanghai 200040, Peoples R China
[2] Fudan Univ, Huashan Hosp, Tradit Chinese Med Dept, 12 Wu Lu Mu Qi M Rd, Shanghai 200040, Peoples R China
关键词
San-Huang decoction; UPLC-ESI-Q-TOF-MS; Chemical profiling; Traditional Chinese medicine formula; TANDEM MASS-SPECTROMETRY; TRADITIONAL CHINESE MEDICINE; RAT PLASMA; LIQUID; ALKALOIDS; IDENTIFICATION; CONSTITUENTS; MS/MS; ARRAY; HPLC;
D O I
10.1016/j.jpba.2016.07.036
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
San-Huang decoction (SHD), a traditional Chinese medical (TCM) formula, is made from five chinese herbs and has been widely used for centuries to treat metabolic syndrome, such as abdominal obesity and nonalcoholic fatty liver disease. In this work, an ultra high performance liquid chromatography coupled with electrospray ionization quadrupole time-of-flight mass spectrometry (UPLC-ESI-Q-TOF-MS) method in both positive and negative ion mode was first employed to rapidly survey the major constituents in SHD. The analysis was performed on a Waters Acquity UPLC BEH C18 column at 45 degrees C within 17 min. 56 compounds in SHD including alkaloids, flavonoids, protostane triterpenoids, coumarins, triterpenoid saponins, organic acids, lignans, lactones and chromones were identified and tentatively characterized by comparison with retention times, accurate mass within 5 ppm error and MS fragmentation ions. Among them, twenty-two compounds were clearly identified mainly by the reference standards. Moreover, this method was respectively applied to determine five batches of SHD and the decoctions of relative individual herbs. These results provide a helpful basic chemical profile for further research of SHD in vivo and exploitation of new drug to treat metabolic syndrome. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:20 / 32
页数:13
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