Original ArticlePharmacognosy MagazineVol. 12 | Issue 48 | 2016 | pp. 282–287Open access
Preparation of Sesquiterpenoids from Tussilago farfara L. by High‑speed Counter‑current Chromatography
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- 2,3*,
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- 1 College of Chemistry and Chemical Engineering, Chongqing University, China.
- 2 Defense Key Disciplines Lab of Novel Micro-nano Devices and System Techonlogy, China.
- 3 International R and D Center of Micro-nano Systems and New Materials Technology, Chongqing, P.R, China.
Published in Pharmacognosy Magazine
Correspondence: Yi Xu
Defense Key Disciplines Lab of Novel Micro-nano Devices and System Techonlogy, China.; International R and D Center of Micro-nano Systems and New Materials Technology, Chongqing, P.R, China.
Email: xuyibbd@sina.com
Copyright: © 2016 Manuscript Technomedia. This is an open access article.
- Published:
- Oct 13, 2016
- Received:
- Jun 23, 2015
How to cite
Cao, K., Xu, Y., Zhao, T., & Zhang, Q. (2016). Preparation of Sesquiterpenoids from Tussilago farfara L. by High‑speed Counter‑current Chromatography. Pharmacognosy Magazine, 12(48), 282–287. https://doi.org/10.4103/0973-1296.192196
Abstract
Background: Sesquiterpenoids, such as tussilagone, has effects of raising blood pressure, antiplatelet aggregation, and anti‑inflammation activities, which is regarded as index compound for quality control of Tussilago farfara L. Objective: This study was aimed to obtain an effective method for fast isolation of sesquiterpenoids from T. farfara L. by high‑speed counter‑current chromatography (HSCCC). Materials and Methods: A solvent optimization method for HSCCC was presented, i.e., the separation factors of compounds after the K values of solvent system should be investigated. Results: A ternary solvent system of n‑hexane:methanol:water (5:8:2, v/v/v) was selected and applied for the HSCCC, and 56 mg of tussilagone (2) was isolated from T. farfara L., along with two other sesquiterpenoids 5.6 mg of 2,2‑dimethyl‑6‑acetylchromanone (1) and 22 mg of 14‑acetoxy‑7 β‑(3’‑ethyl cis‑crotonoyloxy)‑lα‑(2’‑methylbutyryloxy)‑notonipetranone (3) by HSCCC with high purities. Their chemical structures were elucidated by liquid chromatography‑mass spectrometry and nuclear magnetic resonance experiments. Conclusion: These results offered an efficient strategy for preparation of potentially health‑relevant phytochemicals from T. farfara L., which might be used for further chemical research and pharmacological studies by preparative HSCCC.
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Article metadata
| Title | Preparation of Sesquiterpenoids from Tussilago farfara L. by High‑speed Counter‑current Chromatography |
|---|---|
| Authors | Kun Cao; Yi Xu; Tian‑Ming Zhao; Qing Zhang |
| Affiliations | College of Chemistry and Chemical Engineering, Chongqing University, China.; Defense Key Disciplines Lab of Novel Micro-nano Devices and System Techonlogy, China.; International R and D Center of Micro-nano Systems and New Materials Technology, Chongqing, P.R, China. |
| Corresponding author | xuyibbd@sina.com |
| Journal | Pharmacognosy Magazine |
| Volume / Issue | Vol. 12, Issue 48 (2016) |
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