Journal
INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume 312, Issue 1-2, Pages 137-143Publisher
ELSEVIER
DOI: 10.1016/j.ijpharm.2006.01.011
Keywords
baicalein; 2-hydroxypropyl-beta-cyclodextrin; solubilization; co-lyophilized product; pharmacokinetics
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The interaction of 2-hydroxypropyl-beta-cyclodextrin (HP-P-CD) and a poorly water-soluble flavonoid, baicalein (Ba), chemically 5,6,7-trihydroxy flavone in solution and solid-state wits studied. Ba/HP-beta-CD solid systems were prepared by freeze-drying method. The formation of Ba/HP-beta-CD complex in aqueous solution was demonstrated by UV spectroscopy, while Ba/HP-beta-CD co-lyophilized product was characterized by differential scanning calorimetry (DSC) and X-ray diffractometry (XRD). Through complexation with HP-beta-CD, the solubility of Bit in neutral aqueous solution was improved significantly. The phase-solubility profile was A(p)-type, indicating the formation of higher-order complexes or complex aggregates. Ba/HP-beta-CD solid powders were amorphous and show a significantly improved dissolution rate in comparison with free Ba. Comparison of the pharmacokinetics between Ba/HP-beta-CD co-lyophilized product and free Ba was also performed in rats. The concentration of Ba and its mainly conjugated metabolite, 7-O-glucuronide of baicalein (BG) in rat plasma was determined by HPLC method. The in vivo results show that Ba/HP-beta-CD co-lyophilized product exhibits the similar pharmacokinetics as that of free Ba after intravenous administration. Ba/HP-beta-CD co-lyophilized product displays earlier t(max) and higher C-max of BG than free Ba after oral dosing. By comparing the AUC(0-infinity) of BG between oral dosing, the relative bioavailability of Ba/HP-beta-CD co-lyophilized product to free Ba was 165.0%, which highlighted the evidence of significantly improved bioavailability of formulation of Ba with HP-P-Cl). (c) 2006 Elsevier B.V. All rights reserved.
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