Characterization and discrimination of raw and vinegar-baked Bupleuri radix based on UHPLC-Q-TOF-MS coupled with multivariate statistical analysis

被引:29
|
作者
Lei, Tianli [1 ]
Chen, Shifeng [1 ]
Wang, Kai [1 ]
Zhang, Dandan [1 ]
Dong, Lin [1 ]
Lv, Chongning [1 ]
Wang, Jing [2 ]
Lu, Jincai [1 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Tradit Chinese Mat Med, Dept Med Plant, Shenyang 110016, Liaoning, Peoples R China
[2] Shenyang Pharmaceut Univ, Sch Tradit Chinese Mat Med, Dept Pharmaceut Bot, Shenyang, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
Bupleuri radix; chemical marker; multivariate statistical analysis; processing mechanism; UHPLC-q-TOF-MS; SAIKOSAPONINS; METABOLOMICS; IDENTIFICATION; HYPEROSIDE; EXTRACTS; HERBS; CRUDE;
D O I
10.1002/bmc.4044
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Bupleuri Radix is a commonly used herb in clinic, and raw and vinegar-baked Bupleuri Radix are both documented in the Pharmacopoeia of People's Republic of China. According to the theories of traditional Chinese medicine, Bupleuri Radix possesses different therapeutic effects before and after processing. However, the chemical mechanism of this processing is still unknown. In this study, ultra-high-performance liquid chromatography with quadruple time-of-flight mass spectrometry coupled with multivariate statistical analysis including principal component analysis and orthogonal partial least square-discriminant analysis was developed to holistically compare the difference between raw and vinegar-baked Bupleuri Radix for the first time. As a result, 50 peaks in raw and processed Bupleuri Radix were detected, respectively, and a total of 49 peak chemical compounds were identified. Saikosaponin a, saikosaponin d, saikosaponin b(3), saikosaponin e, saikosaponin c, saikosaponin b(2), saikosaponin b(1), 4-O-acetyl-saikosaponin d, hyperoside and 3,4-dimethoxy quercetin were explored as potential markers of raw and vinegar-baked Bupleuri Radix. This study has been successfully applied for global analysis of raw and vinegar-processed samples. Furthermore, the underlying hepatoprotective mechanism of Bupleuri Radix was predicted, which was related to the changes of chemical profiling.
引用
收藏
页数:11
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