Planta Med 2005; 71(9): 803-807
DOI: 10.1055/s-2005-871259
Original Paper
Pharmacology
© Georg Thieme Verlag KG Stuttgart · New York

Bioavailability and Pharmacokinetic Studies of Eurycomanone from Eurycoma longifolia

Bin-Seng Low1 , Bee-Hong Ng1 , Wai-Peng Choy1 , Kah-Hay Yuen1 , Kit-Lam Chan1
  • 1School of Pharmaceutical Sciences, University Sains Malaysia, Penang, Malaysia
Further Information

Publication History

Received: December 9, 2004

Accepted: April 6, 2005

Publication Date:
29 July 2005 (online)

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Abstract

A validated HPLC analysis of eurycomanone (1), a bioactive quassinoid, in rat plasma following oral and intravenous administration of Eurycoma longifolia Jack extract was developed for pharmacokinetic and bioavailability studies. Relatively high plasma eurycomanone concentrations were detected after an intravenous injection of 10 mg/kg extract F2 containing 1.96 mg/kg of the quassinoid. However, it declined rapidly to zero after 8 h. Its mean elimination rate constant (ke), biological half-life (t1/2), volume of distribution (Vd) and clearance (CL) were 0.88 ± 0.19 h-1, 1.00 ± 0.26 h, 0.68 ± 0.30 L/kg and 0.39 ± 0.08 L/h/kg, respectively. Following oral administration of eurycomanone, its Cmax and Tmax values were detected as 0.33 ± 0.03 μg/mL and 4.40 ± 0.98 h, respectively. The plasma concentration of the quassinoid after oral administration was much lower than after intravenous application in spite of the oral dose being 5 times higher. The results indicate that eurycomanone is poorly bioavailable when given orally. A comparison of the AUC0→∞ obtained orally to that obtained after an intravenous administration (normalized for dose differences) revealed that the absolute bioavailability of the compound was low with 10.5 %. Furthermore, the compound appeared to be well distributed in the extravascular fluids because of its relatively high Vd value. The poor oral bioavailability was not attributed to instability problems because eurycomanone has been shown to be stable under different pH conditions. Thus, its poor oral bioavailability may be due to poor membrane permeability in view of its low P value and/or high first-pass metabolism.

References

Kit-Lam Chan

School of Pharmaceutical Sciences

University Sains Malaysia

11800 Penang

Malaysia

Phone: +60-4-657-6836

Fax: +60-4-657-6836

Email: klchan@usm.my