An advanced microencapsulated system: a platform for optimized oral delivery of antidiabetic drug-bile acid formulations

In previous studies, we have shown that a gliclazide-cholic acid derivative (G-CA) mixture resulted in an enhanced ileal permeation of G (ex vivo). When administered orally to diabetic rats, it brought about a significant hypoglycaemic effect. In this study, we aim to create a novel microencapsulate...

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Main Authors: Mooranian, A., Negrulj, R., Mathavan, S., Martinez, J., Sciarretta, J., Chen-Tan, N., Mukkur, T., Mikov, M., Lalic-Popovic, M., Stojancevic, M., Golocorbin-Kon, S., Al-Salami, Hani
Format: Journal Article
Published: TAYLOR & FRANCIS LTD 2015
Online Access:http://hdl.handle.net/20.500.11937/23183
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author Mooranian, A.
Negrulj, R.
Mathavan, S.
Martinez, J.
Sciarretta, J.
Chen-Tan, N.
Mukkur, T.
Mikov, M.
Lalic-Popovic, M.
Stojancevic, M.
Golocorbin-Kon, S.
Al-Salami, Hani
author_facet Mooranian, A.
Negrulj, R.
Mathavan, S.
Martinez, J.
Sciarretta, J.
Chen-Tan, N.
Mukkur, T.
Mikov, M.
Lalic-Popovic, M.
Stojancevic, M.
Golocorbin-Kon, S.
Al-Salami, Hani
author_sort Mooranian, A.
building Curtin Institutional Repository
collection Online Access
description In previous studies, we have shown that a gliclazide-cholic acid derivative (G-CA) mixture resulted in an enhanced ileal permeation of G (ex vivo). When administered orally to diabetic rats, it brought about a significant hypoglycaemic effect. In this study, we aim to create a novel microencapsulated-formulation of G-CA with uniform and coherent structure that can be further tested in our rat model of type 1 diabetes (T1D). We also aim to examine the effect of CA addition to G microcapsules in the morphology, structure and excipients' compatibility of the newly designed microcapsules.
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format Journal Article
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institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T07:47:01Z
publishDate 2015
publisher TAYLOR & FRANCIS LTD
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spelling curtin-20.500.11937-231832017-09-13T13:56:21Z An advanced microencapsulated system: a platform for optimized oral delivery of antidiabetic drug-bile acid formulations Mooranian, A. Negrulj, R. Mathavan, S. Martinez, J. Sciarretta, J. Chen-Tan, N. Mukkur, T. Mikov, M. Lalic-Popovic, M. Stojancevic, M. Golocorbin-Kon, S. Al-Salami, Hani In previous studies, we have shown that a gliclazide-cholic acid derivative (G-CA) mixture resulted in an enhanced ileal permeation of G (ex vivo). When administered orally to diabetic rats, it brought about a significant hypoglycaemic effect. In this study, we aim to create a novel microencapsulated-formulation of G-CA with uniform and coherent structure that can be further tested in our rat model of type 1 diabetes (T1D). We also aim to examine the effect of CA addition to G microcapsules in the morphology, structure and excipients' compatibility of the newly designed microcapsules. 2015 Journal Article http://hdl.handle.net/20.500.11937/23183 10.3109/10837450.2014.915570 TAYLOR & FRANCIS LTD restricted
spellingShingle Mooranian, A.
Negrulj, R.
Mathavan, S.
Martinez, J.
Sciarretta, J.
Chen-Tan, N.
Mukkur, T.
Mikov, M.
Lalic-Popovic, M.
Stojancevic, M.
Golocorbin-Kon, S.
Al-Salami, Hani
An advanced microencapsulated system: a platform for optimized oral delivery of antidiabetic drug-bile acid formulations
title An advanced microencapsulated system: a platform for optimized oral delivery of antidiabetic drug-bile acid formulations
title_full An advanced microencapsulated system: a platform for optimized oral delivery of antidiabetic drug-bile acid formulations
title_fullStr An advanced microencapsulated system: a platform for optimized oral delivery of antidiabetic drug-bile acid formulations
title_full_unstemmed An advanced microencapsulated system: a platform for optimized oral delivery of antidiabetic drug-bile acid formulations
title_short An advanced microencapsulated system: a platform for optimized oral delivery of antidiabetic drug-bile acid formulations
title_sort advanced microencapsulated system: a platform for optimized oral delivery of antidiabetic drug-bile acid formulations
url http://hdl.handle.net/20.500.11937/23183