Original ArticlePharmacognosy MagazineVol. 12 | Issue 46s | 2016 | pp. S102–S108Open access
In vitro Metabolism of Sodium 9‑dehydro‑17‑hydro‑ andrographolide‑19‑yl Sulfate in Rat Liver S9 by Liquid Chromatography–Mass Spectrometry Method
- 2,
- 2,
- 2*,
- 2*
- 1 Department of Traditional Chinese Pharmacy, Jiangxi Provincial Research Institute for Drug Control/Jiangxi Provincial Engineering Research Center for Drug and Medical Device Quality, China.
- 2 Department of Pharmacy, Nanchang University, Nanchang, China.
Published in Pharmacognosy Magazine
Correspondence: Weikang Chen
Department of Pharmacy, Nanchang University, Nanchang, China.
Email: cwkjx@sohu.com
Correspondence: Yuehua Luo
Department of Pharmacy, Nanchang University, Nanchang, China.
Email: meibianluoye@126.com
Copyright: © 2016 Manuscript Technomedia. This is an open access article.
- Published:
- May 11, 2016
- Received:
- Aug 1, 2015
How to cite
Zheng, D., Shao, J., Chen, W., & Luo, Y. (2016). In vitro Metabolism of Sodium 9‑dehydro‑17‑hydro‑ andrographolide‑19‑yl Sulfate in Rat Liver S9 by Liquid Chromatography–Mass Spectrometry Method. Pharmacognosy Magazine, 12(46s), S102–S108. https://doi.org/10.4103/0973-1296.182194
Abstract
Background: Sodium 9‑dehydro‑17‑hydro‑andrographolide‑19‑yl sulfate (DHAS) is the active ingredient of Xiyanping injection, a traditional Chinese medicine in clinical use. However, there has been no report about the metabolic rate and metabolites of DHAS in vitro. Materials and Methods: In this article, DHAS was incubated with rat liver S9, and liquid chromatography/ mass spectrometry (LC/MS) was used for the metabolism study. The residual concentrations of substrate were determined by ultra‑high‑performance liquid chromatography‑electrospray ionization–tandem mass spectrometry method for the metabolic rate study of DHAS in liver S9. Metabolites were identified by the (UPLC‑TOF‑MSE) Ultra-performance liquid chromatography/ quadrupole time-of-flight mass spectrometry method. Results: The calibration curves of DHAS were linear over the concentration range from 0.75 μM to 75.22 μM with correlation coefficients >0.99. The lower limit of quantification was 0.150 μM for DHAS. The determination recoveries of DHAS were in the range of 84.9–90.6%. The t½ and CLint of DHAS in rat liver S9 were 98.6 ± 2.1 min and 3.5 ± 0.1 mL/min/g, respectively. Five metabolites were preliminarily identified based on the high resolution mass spectrum data in comparison with related references. These metabolites were mainly the products of dehydration and hydrogenation of DHAS. Conclusion: The present in vitro metabolic study of DHAS provided valuable information about the metabolic rate and potential metabolites of DHAS, which are important for future in vivo metabolism studies of DHAS and the discovery of more active andrographolide derivatives.
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Article metadata
| Title | In vitro Metabolism of Sodium 9‑dehydro‑17‑hydro‑ andrographolide‑19‑yl Sulfate in Rat Liver S9 by Liquid Chromatography–Mass Spectrometry Method |
|---|---|
| Authors | Dongkun Zheng; Jun Shao; Weikang Chen; Yuehua Luo |
| Affiliations | Department of Traditional Chinese Pharmacy, Jiangxi Provincial Research Institute for Drug Control/Jiangxi Provincial Engineering Research Center for Drug and Medical Device Quality, China.; Department of Pharmacy, Nanchang University, Nanchang, China. |
| Corresponding author | cwkjx@sohu.com |
| Journal | Pharmacognosy Magazine |
| Volume / Issue | Vol. 12, Issue 46s (2016) |
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