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Preparation of fenofibrate nanosuspension and study of its pharmacokinetic behavior in rats
Background: In this study, nanosuspension was prepared to improve the dissolution rate and bioavailability of lipophilic fenofibrate. Method: Melt emulsification method combined with high-pressure homogenization was adapted, and mixture of poloxamer188 and PVP K30 were selected as surfactants. This...
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Published in: | Drug development and industrial pharmacy 2009-07, Vol.35 (7), p.827-833 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Background: In this study, nanosuspension was prepared to improve the dissolution rate and bioavailability of lipophilic fenofibrate. Method: Melt emulsification method combined with high-pressure homogenization was adapted, and mixture of poloxamer188 and PVP K30 were selected as surfactants. This method consumed less energy and was more efficient than traditional homogenization of drug solid particles suspension directly. Results: The dissolution rate of fenofibrate nanosuspension was increased obviously, and the product was evaluated by pharmacokinetic characteristic in rats. The AUC0-36 h and Cmax of nanosuspensions were increased when compared with the reference formulations. No significant differences were found between the two nanosuspensions A and B, of which the mean particle sizes were 356 and 194 nm, respectively. Therefore, nanosuspensions may be a suitable delivery system to improve the bioavailability of those drugs with poor water solubility. |
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ISSN: | 0363-9045 1520-5762 |
DOI: | 10.1080/03639040802623941 |