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Xenobiotica
the fate of foreign compounds in biological systems
Volume 43, 2013 - Issue 11
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Animal Pharmacokinetics and Metabolism

Pharmacokinetics of hederacoside C, an active ingredient in AG NPP709, in rats

, , , , , , & show all
Pages 985-992 | Received 14 Jan 2013, Accepted 18 Mar 2013, Published online: 22 Apr 2013
 

Abstract

1. Hederacoside C (HDC) is one of the active ingredients in Hedera helix leaf extract (Ivy Ex.) and AG NPP709, a new botanical drug to treat acute respiratory infection and chronic inflammatory bronchitis. However, information regarding its pharmacokinetic properties remains limited.

2. Here, we report the pharmacokinetics of HDC in rats after intravenous administration of HDC (3, 12.5, and 25 mg/kg) and after oral administration of HDC, Ivy Ex., and AG NPP709 (equivalent to 12.5, 25, and 50 mg/kg HDC).

3. Linear pharmacokinetics of HDC were identified upon its intravenous administration at doses of 3–25 mg/kg. Intravenous administration of HDC results in relatively slow clearance (1.46–2.08 mL/min/kg) and a small volume of distribution at steady state (138–222 mL/kg), while oral administration results in a low absolute oral bioavailability (F) of 0.118–0.250%. The extremely low F of HDC may be due to poor absorption of HDC from the gastrointestinal (GI) tract and/or its decomposition therein.

4. The oral pharmacokinetics of HDC did not differ significantly among pure HDC, Ivy Ex., and AG NPP709.

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