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dc.contributor.authorMooranian, A.
dc.contributor.authorZamani, N.
dc.contributor.authorMikov, M.
dc.contributor.authorGolocorbin-Kon, S.
dc.contributor.authorStojanovic, G.
dc.contributor.authorArfuso, Frank
dc.contributor.authorAl-Salami, Hani
dc.date.accessioned2018-12-13T09:14:24Z
dc.date.available2018-12-13T09:14:24Z
dc.date.created2018-12-12T02:47:04Z
dc.date.issued2018
dc.identifier.citationMooranian, A. and Zamani, N. and Mikov, M. and Golocorbin-Kon, S. and Stojanovic, G. and Arfuso, F. and Al-Salami, H. 2018. Novel nano-encapsulation of probucol in microgels: scanning electron micrograph characterizations, buoyancy profiling, and antioxidant assay analyses. Artificial Cells, Nanomedicine and Biotechnology.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/72760
dc.identifier.doi10.1080/21691401.2018.1511571
dc.description.abstract

© 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group. Smart polymers such as Eudragit (ED) have shown potential applications in oral drug delivery and targeted release. Probucol (PB) is a lipophilic drug used for hypercholesterolemia and possesses desirable antidiabetic effects such as antioxidant and cell protective effects. PB is highly hydrophobic and has poor bioavailability with significant inter- and intra-patient absorption, limiting its clinical applications in diabetes. This study aimed to design and analyse new PB-ED formulations with or without the absorption-enhancer chenodeoxycholic acid (CDCA). Sodium alginate-based microcapsules containing three different ED polymers (NM30D, RL30D and RS30D) were investigated with or without CDCA via scanning electron microscopy, energy dispersive X-ray spectroscopy (EDXR), confocal microscopy, osmotic stability, mechanical properties, buoyancy, release profiles (pH: 7.4), thermal stability and antioxidant effects. The effects of microcapsules on pancreatic ß-cell survival, function, inflammatory profile and PB cellular uptake were analysed. All microcapsules showed uniform morphology and surface topography with CDCA being distributed evenly throughout the microcapsules. Osmotic stability was significantly improved in PB-NM30D and PB-RL30D microcapsules (p <.01 and p <.05, respectively), and PB-NM30D microcapsules displayed low buoyancy (p <.01). CDCA improved PB-NM30D effects on pancreatic ß-cell function and bioenergetics, which suggests potential application of PB-NM30D-CDCA in PB delivery and diabetes treatment.

dc.publisherTaylor & Francis Inc.
dc.titleNovel nano-encapsulation of probucol in microgels: scanning electron micrograph characterizations, buoyancy profiling, and antioxidant assay analyses
dc.typeJournal Article
dcterms.source.issn2169-1401
dcterms.source.titleArtificial Cells, Nanomedicine and Biotechnology
curtin.departmentSchool of Pharmacy and Biomedical Sciences
curtin.accessStatusFulltext not available


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