Planta Med 2011; 77(16): 1794-1799
DOI: 10.1055/s-0030-1271120
Pharmacokinetic Investigations
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Absolute/Relative Bioavailability and Metabolism of Dodeca-2E,4E,8Z,10E/Z-Tetraenoic Acid Isobutylamides (Tetraenes) after Intravenous and Oral Single Doses to Rats

Karin Ardjomand-Woelkart1 , 5 , Manfred Kollroser2 , Christoph Magnes3 , Frank Sinner3 , Reginald F. Frye4 , Hartmut Derendorf1 , Rudolf Bauer5 , Veronika Butterweck1
  • 1Department of Pharmaceutics, College of Pharmacy, University of Florida, Gainesville, Florida, USA
  • 2Institute of Forensic Medicine, Medical University of Graz, Graz, Austria
  • 3Joanneum Research, Institute of Medical Technologies and Health Management, Graz, Austria
  • 4Department of Pharmacotherapy and Translational Research, College of Pharmacy, University of Florida, Gainesville, Florida, USA
  • 5Institute of Pharmaceutical Sciences, Department of Pharmacognosy, Karl-Franzens-University Graz, Graz, Austria
Weitere Informationen

Publikationsverlauf

received February 12, 2011 revised April 17, 2011

accepted April 26, 2011

Publikationsdatum:
20. Mai 2011 (online)

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Abstract

The present study assessed the absolute and relative bioavailabilities of dodeca-2E,4E,8Z,10E/Z-tetraenoic acid isobutylamides (tetraenes), the main bioactive constituents in Echinacea, administered as pure compounds or in the form of an Echinacea purpurea root extract preparation. Tetraenes were administered orally by gavage or intravenously in a dose of 0.75 mg/kg. The extract was administered orally in a dose of 158.6 mg/kg which corresponds to the same amount of tetraenes. Pharmacokinetic parameters of tetraenes were calculated by non-compartmental analysis using WinNonlin® 5.2 software. Mean dodeca-2E,4E,8Z,10E/Z-tetraenoic acid isobutylamide dose-normalized plasma area under the concentration-time curve (AUC0–∞/dose) was 3.24 ± 0.32 min · ng/mL/µg and 0.95 ± 0.16 min · ng/mL/µg after iv and oral administrations, respectively, and 1.53 ± 0.18 min · ng/mL/µg after oral administration of the Echinacea root extract. The absolute oral bioavailability of dodeca-2E,4E,8Z,10E/Z-tetraenoic acid isobutylamides was 29.2 ± 2.3 %, which was increased to 47.1 ± 7.2 % (1.6-fold) by administration of the Echinacea extract. Administration of an Echinacea extract increased blood exposure with no impact on Cmax, but prolonged the elimination half-life to 123.3 ± 15.7 min in comparison to 35.8 ± 6.5 min after administration of the pure dodeca-2E,4E,8Z,10E/Z-tetraenoic acid isobutylamides.

References

Dr. Veronika Butterweck, Associate Professor of Pharmaceutics

Department of Pharmaceutics, College of Pharmacy
University of Florida

1600 SW Archer Road

Gainesville, Florida 32610

USA

Telefon: +1 35 22 73 78 59

Fax: +1 35 22 73 78 54

eMail: butterwk@cop.ufl.edu