TY - JOUR
T1 - Sustained release of targeted cardiac therapy with a replenishable implanted epicardial reservoir /692/4019/2773 /639/301/54/152 /14/5 /14/35 /14/63 /59/5 /96/106 /96/100 /96/34 article
AU - Whyte, William
AU - Roche, Ellen T.
AU - Varela, Claudia E.
AU - Mendez, Keegan
AU - Islam, Shahrin
AU - O'Neill, Hugh
AU - Weafer, Fiona
AU - Shirazi, Reyhaneh Neghabat
AU - Weaver, James C.
AU - Vasilyev, Nikolay V.
AU - McHugh, Peter E.
AU - Murphy, Bruce
AU - Duffy, Garry P.
AU - Walsh, Conor J.
AU - Mooney, David J.
N1 - Publisher Copyright:
© 2018 The Author(s).
PY - 2018/6/1
Y1 - 2018/6/1
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/85048370295
U2 - 10.1038/s41551-018-0247-5
DO - 10.1038/s41551-018-0247-5
M3 - Article
SN - 2157-846X
VL - 2
SP - 416
EP - 428
JO - Nature Biomedical Engineering
JF - Nature Biomedical Engineering
IS - 6
ER -