Development and validation of a sensitive liquid chromatography‐tandem mass spectrometry method for the assay of 12 substances in rat plasma and its application to rat pharmacokinetics of Epimedium and Psoraleae Fructus herb pair after oral administration

Author:

Wang Linwei12,Yin Xiaoying13,Liu Huan2,Wang Yangyang2,Li Zhixiong2,Zhao Yuxuan2,Xu Haibo2,Huang Chenggang24,Diao Xingxing245ORCID

Affiliation:

1. College of Chemistry and Chemical Engineering Shanghai University of Engineering Science Shanghai China

2. Shanghai Institute of Materia Medica Chinese Academy of Sciences Shanghai China

3. Shanghai Frontiers Science Research Center for Drug ability of Cardiovascular noncoding RNA Shanghai China

4. University of Chinese Academy of Sciences Beijing China

5. XenoFinder Co. Ltd Suzhou China

Abstract

Epimedium (EM) and Psoraleae Fructus (PF) are a traditional herb combination often used as a fixed form to treat osteoporosis disease in the clinic. However, the intricate interactions of this pair remain unknown. In our study, we undertook a comprehensive examination of their compatibility behaviors. Concurrently, a precise and sensitive quantitation method was successfully developed and validated using liquid chromatography‐tandem mass spectrometry for the determination of 12 components. This method was applied in analyzing herbal extracts and biological samples (both in the portal vein and systemic plasma), which was also used to study the pharmacokinetics of the herb pair. The results indicated that the combination of EM and PF enhanced the dissolution of chemical components from PF in extracts, but it had a negligible influence on the contents of the components from EM. On the contrary, the in vivo exposure of the lowly exposed EM flavonoids significantly increased following the combination of EM and PF, whereas the highly exposed psoralen and isopsoralen were greatly reduced. These interactions might be crucial for the synergy and toxicity reduction of the herbal pair in disease treatment, which pave the way for further exploration into the clinical application and pharmacological mechanisms of EM and PF.

Funder

National Basic Research Program of China

National Natural Science Foundation of China

Key Technologies Research and Development Program

Publisher

Wiley

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