Supramolecular Complex of Ibuprofen with Larch Polysaccharide Arabinogalactan: Studies on Bioavailability and Pharmacokinetics

Overview

Journal Eur J Drug Metab Pharmacokinet

Date 2016 Jun 29

PMID 27351190

Citations 8

Authors

Mikhail V Khvostov

Sergey A Borisov

Tatjana G Tolstikova

Alexander V Dushkin

Biligma D Tsyrenova

Yulia S Chistyachenko

Nikolay E Polyakov

Galina G Dultseva

Andrey A Onischuk

Sergey V Ankov

Affiliations

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Abstract

Background And Objectives: In the present work, pharmacological and pharmacokinetic properties of the supramolecular complex of non-steroid anti-inflammatory drug ibuprofen (IBU) with natural polysaccharide arabinogalactan (AG) were studied. The main goals of such complexation were the increase of ibuprofen's bioavailability and decrease its effective dose after oral administration.

Methods: The complex with mass ratio as IBU:AG 1:10 was obtained by mechanochemical synthesis and characterized by water solubility, electron microscopy, differential scanning calorimetry, X-ray powder diffraction analysis and H-nuclear magnetic resonance spectroscopy. Different animal models of pain and inflammation was used to investigate IBU:AG biological effects. Plasma concentration of IBU and its pharmacokinetic parameters were evaluated after oral introduction.

Results: It was found that ibuprofen's effective analgesic and anti-inflammatory dose decreased twofold after its introduction as a complex with AG. The reason of this difference is due to the increase of ibuprofen concentration in rats' plasma: C of IBU at doses of 20 and 40 mg/kg was found as 0.088 and 0.132 μg/ml, whereas C of IBU in the complex form was 0.103 and 0.160 μg/ml, respectively.

Conclusions: Thus, we have shown that complexation of the IBU with AG results in its bioavailability increase, reduction of the effective dose and should decrease toxic side effects.

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