Alginate-combined cholic acid increased insulin secretion of microencapsulated mouse cloned pancreatic ß cells
dc.contributor.author | Mooranian, A. | |
dc.contributor.author | Negrulj, R. | |
dc.contributor.author | Takechi, R. | |
dc.contributor.author | Jamieson, E. | |
dc.contributor.author | Morahan, G. | |
dc.contributor.author | Al-Salami, Hani | |
dc.date.accessioned | 2017-10-30T08:16:33Z | |
dc.date.available | 2017-10-30T08:16:33Z | |
dc.date.created | 2017-10-30T08:03:06Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | Mooranian, A. and Negrulj, R. and Takechi, R. and Jamieson, E. and Morahan, G. and Al-Salami, H. 2017. Alginate-combined cholic acid increased insulin secretion of microencapsulated mouse cloned pancreatic ß cells. Therapeutic Delivery. 8 (10): pp. 833-842. | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/57300 | |
dc.identifier.doi | 10.4155/tde-2017-0042 | |
dc.description.abstract |
© 2017 2017 Future Science Ltd. Aim: A semisynthetic primary bile acid (PBA) has exerted hypoglycemic effects in Type 1 diabetic animals, which were hypothesized to be due to its anti-inflammatory and cellular glucose-regulatory effects. Thus, the research purpose aimed to examine antidiabetic effects of a PBA, in terms of cellular inflammation and survival and insulin release, in the context of supporting ß-cell delivery and Type 1 diabetic treatment. Materials & methods: 10 formulations were prepared, five without PBA (control) and five with PBA (test). Formulations were used to microencapsulate pancreatic ß cells and the microcapsules were examined for morphology, cell viability, insulin release and inflammation. Results & conclusion: PBA improved cell viability, insulin release and reduced inflammation in a formulation-dependent manner, which suggests potential use in cell delivery and diabetes treatment. | |
dc.title | Alginate-combined cholic acid increased insulin secretion of microencapsulated mouse cloned pancreatic ß cells | |
dc.type | Journal Article | |
dcterms.source.volume | 8 | |
dcterms.source.number | 10 | |
dcterms.source.startPage | 833 | |
dcterms.source.endPage | 842 | |
dcterms.source.issn | 2041-5990 | |
dcterms.source.title | Therapeutic Delivery | |
curtin.department | School of Pharmacy | |
curtin.accessStatus | Fulltext not available |
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