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Formulation and in vivo human bioavailability of dissolving tablets containing a self-nanoemulsifying itraconazole solid dispersion without precipitation in simulated gastrointestinal fluid

Authors
Piao, Zong-ZhuChoe, Jae-SeungOh, Kyung TeakRhee, Yun-SeokLee, Beom-Jin
Issue Date
Jan-2014
Publisher
ELSEVIER SCIENCE BV
Keywords
Poorly water-soluble drug; Self-nanoemulsifying solid dispersion; Enhanced dissolution; Precipitation and crystallisation; In vivo oral bioavailability
Citation
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, v.51, no.1, pp 67 - 74
Pages
8
Journal Title
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES
Volume
51
Number
1
Start Page
67
End Page
74
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/12581
DOI
10.1016/j.ejps.2013.08.037
ISSN
0928-0987
1879-0720
Abstract
To investigate the performance of a solid-state self-nanoemulsifying system with no precipitation in gastric and intestinal fluid, itraconazole (ITZ) was selected as a model drug because of its practically insoluble nature in intestinal fluid. A self-nanoemulsifying ITZ solid dispersion (SNESD) system was prepared as follows: (1) establishment of self-nanoemulsifying composition via the hot melting method, (2) solidification with fumed silicon dioxide (Aerosil 300) via adsorption to prepare SNESD and (3) preparation of a directly compressible tablet containing SNESD. This SNESD was easily formulated in the form of a dissolving tablet and provided a favourable nanoemulsifying microenvironment with no precipitation in the testing media. The SNESD and SNESD-loaded tablet displayed highly enhanced dissolution via nanomisation (266.8 nm and 258.3 nm at 60 min and 120 min, respectively), whereas the drug alone or a reference ITZ Sporanox (R) capsule displayed very low dissolution and precipitated immediately in intestinal fluid. Drug precipitation in intestinal fluid may affect the in vivo performance of poorly soluble weakly basic drugs and was estimated according to the crystal growth theory. The superdisintegrant and surfactant in the formulation of the tablet were very crucial to the dissolution of the SNESD-loaded tablet. The drug contents and dissolution rates of the SNESD-loaded tablets were also stable during storage in terms of dissolution and drug content. The SNESD-loaded tablet displayed significantly increased oral bioavailability in healthy human volunteers compared with the reference Sporanox (R) capsule. The current solid-state SNESD-loaded tablet could provide an alternative to liquid-based emulsifying preparations for various poorly water-soluble drugs without precipitation in testing media. (C) 2013 Elsevier B.V. All rights reserved.
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Oh, Kyung Taek
대학원 (글로벌혁신신약학과)
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