| Literature DB >> 31011199 |
William Whyte1,2,3,4,5, Ellen T Roche1,2,6,7,8,9,10, Claudia E Varela8,10, Keegan Mendez1,2, Shahrin Islam9, Hugh O'Neill3, Fiona Weafer6, Reyhaneh Neghabat Shirazi6, James C Weaver1,2, Nikolay V Vasilyev11, Peter E McHugh6, Bruce Murphy4,5, Garry P Duffy12,13,14,15, Conor J Walsh16,17, David J Mooney18,19.
Abstract
The clinical translation of regenerative therapy for the diseased heart, whether in the form of cells, macromolecules or small molecules, is hampered by several factors: the poor retention and short biological half-life of the therapeutic agent, the adverse side effects from systemic delivery, and difficulties with the administration of multiple doses. Here, we report the development and application of a therapeutic epicardial device that enables sustained and repeated administration of small molecules, macromolecules and cells directly to the epicardium via a polymer-based reservoir connected to a subcutaneous port. In a myocardial infarct rodent model, we show that repeated administration of cells over a four-week period using the epicardial reservoir provided functional benefits in ejection fraction, fractional shortening and stroke work, compared to a single injection of cells and to no treatment. The pre-clinical use of the therapeutic epicardial reservoir as a research model may enable insights into regenerative cardiac therapy, and assist the development of experimental therapies towards clinical use.Entities:
Mesh:
Year: 2018 PMID: 31011199 DOI: 10.1038/s41551-018-0247-5
Source DB: PubMed Journal: Nat Biomed Eng ISSN: 2157-846X Impact factor: 25.671