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

© 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 an...

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Main Authors: Mooranian, A., Zamani, N., Mikov, M., Golocorbin-Kon, S., Stojanovic, G., Arfuso, Frank, Al-Salami, Hani
Format: Journal Article
Published: 2018
Online Access:http://hdl.handle.net/20.500.11937/71355
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author Mooranian, A.
Zamani, N.
Mikov, M.
Golocorbin-Kon, S.
Stojanovic, G.
Arfuso, Frank
Al-Salami, Hani
author_facet Mooranian, A.
Zamani, N.
Mikov, M.
Golocorbin-Kon, S.
Stojanovic, G.
Arfuso, Frank
Al-Salami, Hani
author_sort Mooranian, A.
building Curtin Institutional Repository
collection Online Access
description © 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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institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T10:47:53Z
publishDate 2018
recordtype eprints
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spelling curtin-20.500.11937-713552019-04-08T04:04:03Z Eudragit®-based microcapsules of probucol with a gut-bacterial processed secondary bile acid Mooranian, A. Zamani, N. Mikov, M. Golocorbin-Kon, S. Stojanovic, G. Arfuso, Frank Al-Salami, Hani © 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. 2018 Journal Article http://hdl.handle.net/20.500.11937/71355 10.4155/tde-2018-0036 restricted
spellingShingle Mooranian, A.
Zamani, N.
Mikov, M.
Golocorbin-Kon, S.
Stojanovic, G.
Arfuso, Frank
Al-Salami, Hani
Eudragit®-based microcapsules of probucol with a gut-bacterial processed secondary bile acid
title Eudragit®-based microcapsules of probucol with a gut-bacterial processed secondary bile acid
title_full Eudragit®-based microcapsules of probucol with a gut-bacterial processed secondary bile acid
title_fullStr Eudragit®-based microcapsules of probucol with a gut-bacterial processed secondary bile acid
title_full_unstemmed Eudragit®-based microcapsules of probucol with a gut-bacterial processed secondary bile acid
title_short Eudragit®-based microcapsules of probucol with a gut-bacterial processed secondary bile acid
title_sort eudragit®-based microcapsules of probucol with a gut-bacterial processed secondary bile acid
url http://hdl.handle.net/20.500.11937/71355