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dc.contributor.authorMooranian, Armin
dc.contributor.authorNegrulj, Rebecca
dc.contributor.authorJamieson, E.
dc.contributor.authorMorahan, G.
dc.contributor.authorAl-Salami, Hani
dc.date.accessioned2017-01-30T11:47:43Z
dc.date.available2017-01-30T11:47:43Z
dc.date.created2016-06-15T19:30:18Z
dc.date.issued2016
dc.identifier.citationMooranian, A. and Negrulj, R. and Jamieson, E. and Morahan, G. and Al-Salami, H. 2016. Biological assessments of encapsulated pancreatic ß-Cells: Their potential transplantation in diabetes. Cellular and Molecular Bioengineering. [In Press].
dc.identifier.urihttp://hdl.handle.net/20.500.11937/15066
dc.identifier.doi10.1007/s12195-016-0441-z
dc.description.abstract

© 2016. Biomedical Engineering Society. Microencapsulation of pancreatic islets has been considered as a promising method for cell transplantation and diabetes treatment. However, in vivo trials to date have been hampered by fibrotic overgrowth and very limited to no success, long-term. Future success requires suitable microencapsulating method and possibly a simplified and suitable formulation which will produce a microcapsule that provides an immunobarrier, maintain full ß-cell functionality whilst also reducing the inflammatory processes that induce fibrosis. In multiple studies, we screened various formulations and microencapsulating methods, and obtained promising results using bile acid-based microcapsules containing ß-cells, in terms of cell functions and insulin release. Thus, this study aimed to refine further the microencapsulating method using a simple alginate-poly-l-ornithine formulation and test the effect of adding a promising bile acid, ursodeoxycholic acid (UDCA), on cell functions. Using Büchi concentric nozzle, viable NIT-1 cells were microencapsulated using alginate-poly-l-ornithine, with or without UDCA at a ratio of 1:1.2 or 1:1.2:4. Screening for nozzle temperature and nozzle-gelation bath distance was carried out to form best microcapsules. Microcapsules were cultured for 48 h and examined for size and surface morphology, chemical profiling and ß-cell viability. Culture supernatants were examined for insulin and inflammatory cytokines. When using 30 °C nozzle-temperature and 5 cm nozzle-gelation bath distance, in the presence of the bile acid, cell mitochondrial activities and insulin production were optimised. Under deployed microencapsulating method with nozzle-temperature of 30 °C and nozzle-gelation bath distance of 5 cm, the incorporation of the bile acid into the microcapsules resulted in enhanced ß-cell survival, function and improved overall biocompatibility supporting potential applications in transplantation.

dc.publisherSpringer New York LLC
dc.titleBiological Assessments of Encapsulated Pancreatic ß-Cells: Their Potential Transplantation in Diabetes
dc.typeJournal Article
dcterms.source.startPage1
dcterms.source.endPage8
dcterms.source.issn1865-5025
dcterms.source.titleCellular and Molecular Bioengineering
curtin.departmentSchool of Pharmacy
curtin.accessStatusFulltext not available


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