Pharmacokinetics and oral bioavailability of epimedin C after oral administration of epimedin C and Herba Epimedii extract in rats.

Abstract

Epimedin C, an ingredient of Herba Epimedii, has potential for treatment of cardiovascular disease and bone loss. However, there is still no sensitive analytical method to monitor epimedin C in biological samples. The goal of this study was to develop a sensitive and reliable method based on a LC-MS/MS for evaluating the pharmacokinetics of epimedin C after administration of Herba Epimedii in rat. Electrospray ionization in positive-ion mode and multiple reaction monitoring were used to identify and quantitate active components. Analytes were separated by a reverse-phase C18 column. Liquid-liquid extraction using ethyl acetate, evaporation and reconstitution was used to plasma sample preparation. Mass transition of precursor ion → product ion pairs were monitored at m/z 823.4 → 313.1 for epimedin C and m/z 237.1 → 178.9 for carbamazepine (internal standard). A calibration curve gave good linearity (r > 0.999) over the concentration range 2.5-500 ng/mL. Pharmacokinetic data demonstrated that there was rapid distribution and slow elimination after epimedin C administration (1 mg/kg, i.v.). Oral bioavailabilities of epimedin C in the pure compound and in the Herba Epimedii were around 0.58% and 0.13%, respectively. The result suggests that other herbal ingredients of Herba Epimedii may suppress the oral bioavailability of epimedin C.

• Authors: Chia-Jung Lee, Yu-Tse Wu, Thomas Y Hsueh, Lie-Chwen Lin, Tung-Hu Tsai
• Journal: Biomedical chromatography : BMC (Biomed Chromatogr) Vol. 28 Issue 5 Pg. 630-6 (May 2014) ISSN: 1099-0801 [Electronic] England
• PMID: 24264996 (Publication Type: Evaluation Study, Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2013 John Wiley & Sons, Ltd.

Chemical References

• Drugs, Chinese Herbal
• Flavonoids
• epimedii flavone
• epimedin C

Topics

• Administration, Oral
• Animals
• Biological Availability
• Chromatography, High Pressure Liquid (methods)
• Drugs, Chinese Herbal (administration & dosage, chemistry, pharmacokinetics)
• Flavonoids (administration & dosage, pharmacokinetics)
• Male
• Rats
• Rats, Sprague-Dawley
• Tandem Mass Spectrometry (methods)