Advanced bile acid-based multi-compartmental microencapsulated pancreatic ß-cells integrating a polyelectrolyte-bile acid formulation, for diabetes treatment.
dc.contributor.author | Mooranian, A. | |
dc.contributor.author | Negrulj, R. | |
dc.contributor.author | Chen-Tan, N. | |
dc.contributor.author | Fakhoury, M. | |
dc.contributor.author | Arfuso, F. | |
dc.contributor.author | Jones, Franca | |
dc.contributor.author | Al-Salami, H. | |
dc.date.accessioned | 2017-01-30T11:36:08Z | |
dc.date.available | 2017-01-30T11:36:08Z | |
dc.date.created | 2015-10-29T04:09:49Z | |
dc.date.issued | 2014 | |
dc.identifier.citation | Mooranian, A. and Negrulj, R. and Chen-Tan, N. and Fakhoury, M. and Arfuso, F. and Jones, F. and Al-Salami, H. 2014. Advanced bile acid-based multi-compartmental microencapsulated pancreatic ß-cells integrating a polyelectrolyte-bile acid formulation, for diabetes treatment.Artificial Cells, Nanomedicine, and Biotechnology. [In Press]. | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/13290 | |
dc.identifier.doi | 10.3109/21691401.2014.971806 | |
dc.description.abstract |
This study utilized the Seahorse Analyzer to examine the effect of the bile acid ursodeoxycholic acid (UDCA), on the morphology, swelling, stability, and size of novel microencapsulated ß-cells, in real-time. UDCA was conjugated with fluorescent compounds, and its partitioning within the microcapsules was examined using confocal microscopy. UDCA produced microcapsules with good morphology, better mechanical strength (p < 0.01), and reduced swelling properties (p < 0.01), but lower cell viability (p < 0.05) and cell count per microcapsule (p < 0.01). UDCA reduced the cells' biochemical activities, mitochondrial respiration, and energy production, post-microencapsulation. This is the first time biological functions of microencapsulated ß-cells have been analyzed in real-time. | |
dc.title | Advanced bile acid-based multi-compartmental microencapsulated pancreatic ß-cells integrating a polyelectrolyte-bile acid formulation, for diabetes treatment. | |
dc.type | Journal Article | |
dcterms.source.startPage | 1 | |
dcterms.source.endPage | 8 | |
dcterms.source.title | Artif Cells Nanomed Biotechnol | |
curtin.department | Nanochemistry Research Institute | |
curtin.accessStatus | Fulltext not available |