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Development of omega-3 phospholipid-based solid dispersion of fenofibrate for the enhancement of oral bioavailability

Authors
Yang, LiangShao, YatingHan, Hyo-Kyung
Issue Date
12-Oct-2015
Publisher
ELSEVIER SCIENCE BV
Keywords
Antisolvent; Omega-3 phospholipids; Fenofibrate; Dissolution; Bioavailability
Citation
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, v.78, pp 103 - 110
Pages
8
Indexed
SCI
SCIE
SCOPUS
Journal Title
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES
Volume
78
Start Page
103
End Page
110
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/25247
DOI
10.1016/j.ejps.2015.07.007
ISSN
0928-0987
1879-0720
Abstract
This research aimed to develop the omega-3 phospholipids based solid dispersion to improve the oral bioavailability of fenofibrate. The omega-3 phospholipids based solid dispersion formulation (OPSD) was prepared by an antisolvent precipitation with immediate freeze-drying and the optimal composition of the formulation was determined as the ratios of sucrose to krill oil of 5:1 (w/w), krill oil to fenofibrate of 1.5:1 (w/w), and antisolvent to solvent of 6:4 (v/v). The developed OPSD formulation was characterized by using scanning electron microscopy (SEM), X-ray powder diffraction (XRPD), and differential scanning calorimetry (DSC), which indicated the crystalline state of fenofibrate in the OPSD. The drug release profiles were also examined at different pHs. The OPSD achieved almost complete dissolution within 15 min, while the untreated powder and physical mixture exhibited minimal dissolution (less than 10% even after 2 h). Furthermore, this formulation effectively increased the oral drug exposure in rats, as the C-max and AUC of fenofibric acid (an active metabolite) were enhanced by approximately 6-7 folds. These results suggest that the OPSD formulation should be promising for improving the oral bioavailability of fenofibrate. (C) 2015 Elsevier B.V. All rights reserved.
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