Dynamic actuation enhances transport and extends therapeutic lifespan in an implantable drug delivery platform

Author:

Whyte WilliamORCID,Goswami DebkalpaORCID,Wang Sophie X.ORCID,Fan Yiling,Ward Niamh A.ORCID,Levey Ruth E.,Beatty RachelORCID,Robinson Scott T.,Sheppard Declan,O’Connor Raymond,Monahan David S.ORCID,Trask LesleyORCID,Mendez Keegan L.,Varela Claudia E.,Horvath Markus A.,Wylie Robert,O’Dwyer Joanne,Domingo-Lopez Daniel A.ORCID,Rothman Arielle S.ORCID,Duffy Garry P.,Dolan Eimear B.ORCID,Roche Ellen T.ORCID

Abstract

AbstractFibrous capsule (FC) formation, secondary to the foreign body response (FBR), impedes molecular transport and is detrimental to the long-term efficacy of implantable drug delivery devices, especially when tunable, temporal control is necessary. We report the development of an implantable mechanotherapeutic drug delivery platform to mitigate and overcome this host immune response using two distinct, yet synergistic soft robotic strategies. Firstly, daily intermittent actuation (cycling at 1 Hz for 5 minutes every 12 hours) preserves long-term, rapid delivery of a model drug (insulin) over 8 weeks of implantation, by mediating local immunomodulation of the cellular FBR and inducing multiphasic temporal FC changes. Secondly, actuation-mediated rapid release of therapy can enhance mass transport and therapeutic effect with tunable, temporal control. In a step towards clinical translation, we utilise a minimally invasive percutaneous approach to implant a scaled-up device in a human cadaveric model. Our soft actuatable platform has potential clinical utility for a variety of indications where transport is affected by fibrosis, such as the management of type 1 diabetes.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary

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