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    Eudragit®-based microcapsules of probucol with a gut-bacterial processed secondary bile acid

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    Authors
    Mooranian, A.
    Zamani, N.
    Mikov, M.
    Golocorbin-Kon, S.
    Stojanovic, G.
    Arfuso, Frank
    Al-Salami, Hani
    Date
    2018
    Type
    Journal Article
    
    Metadata
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    Citation
    Mooranian, A. and Zamani, N. and Mikov, M. and Golocorbin-Kon, S. and Stojanovic, G. and Arfuso, F. and Al-Salami, H. 2018. Eudragit®-based microcapsules of probucol with a gut-bacterial processed secondary bile acid. Therapeutic Delivery. 9 (11): pp. 811-821.
    Source Title
    Therapeutic Delivery
    DOI
    10.4155/tde-2018-0036
    ISSN
    2041-5990
    School
    School of Pharmacy and Biomedical Sciences
    URI
    http://hdl.handle.net/20.500.11937/71355
    Collection
    • Curtin Research Publications
    Abstract

    © 2018 Newlands Press. Aim: Deoxycholic acid (DCA) has improved gliclazide oral absorption, while Eudragit® (ED) polymers have improved formulation stability of antidiabetic drugs. The aim of the study is to test if DCA and ED encapsulation will optimize the release and stability of the potential antidiabetic drug probucol (PB). Materials & methods: The PB formulations were prepared using ED polymers and DCA, and formulations were analyzed for their rheological and biological properties. Results: Rheological properties and size distribution were similar among all groups. ß-cell survival and biological activities were best with NM30D microcapsules. The inflammatory profile and oxidative stress effects of microcapsules remained similar among all groups. Conclusion: ED NM30D and DCA incorporation can exert positive and stabilizing effects on PB oral microcapsules.

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