Korean J Physiol Pharmacol.  2004 Feb;8(1):65-67.

Pharmacokinetics of Dehydroevodiamine Following Intravenous Administration in Rats

Affiliations
  • 1Department of Pharmacology, College of Medicine, The Catholic University of Korea, Seoul 137-701, Korea. sbl@catholic.ac.kr

Abstract

Dehydroevodiamine (DHED) is one of the bioactive components of the Chinese herbal medicine Wu-chu-yu-tang that has been shown to produce various pharmacological effects. In the present study, we investigated the pharmacokinetics of DHED after intravenous administration of two doses (2.5 and 5 mg/kg) in anesthetized rats. The plasma concentration of DHED was measured by reverse-phase high-performance liquid chromatography with UV detection. The mean area under the curve of the time-concentration profile was 21.9 and 53.9 microgram-min/ml after the 2.5- and 5-mg/kg doses, respectively, and the volume of distribution was 1584.9 and 1580.6 ml following 2.5- and 5-mg/kg doses, respectively. Plasma concentration profiles versus time were compatible with a two-compartment model and first-order kinetics. The terminal elimination half-life was 91.8+/-16.6 min and 78.7+/-11.9 min in the dose of 2.5 and 5 mg/kg, respectively. This is the first report to study the pharmacokinetics of DHED in animals.

Keyword

Dehydroevodiamine; Pharmacokinetics; Wu-chu-yu; HPLC; Intravenous injection; Rats

MeSH Terms

Administration, Intravenous*
Animals
Asian Continental Ancestry Group
Chromatography, High Pressure Liquid
Chromatography, Liquid
Half-Life
Herbal Medicine
Humans
Injections, Intravenous
Kinetics
Pharmacokinetics*
Plasma
Rats*
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