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Abstract
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 β-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 β-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 β-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 β-cell survival, function and improved overall biocompatibility supporting potential applications in transplantation. © 2016, Biomedical Engineering Society.
Original language | English |
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Pages (from-to) | 530-537 |
Number of pages | 8 |
Journal | Cellular and Molecular Bioengineering |
Volume | 9 |
Issue number | 4 |
DOIs | |
Publication status | Published - 1 Dec 2016 |
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Dive into the research topics of 'Biological assessments of encapsulated pancreatic β-cells: their potential transplantation in diabetes'. Together they form a unique fingerprint.Projects
- 1 Finished
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Pathogenesis Based Treatment of Type 1 Diabetes
National Health & Medical Research Council NHMRC
1/01/13 → 31/12/17
Project: Research