Soft robot–mediated autonomous adaptation to fibrotic capsule formation for improved drug delivery

Author:

Beatty Rachel12ORCID,Mendez Keegan L.34ORCID,Schreiber Lucien H. J.1,Tarpey Ruth156ORCID,Whyte William4ORCID,Fan Yiling7ORCID,Robinson Scott T.12ORCID,O’Dwyer Joanne1ORCID,Simpkin Andrew J.8ORCID,Tannian Joseph1,Dockery Peter1,Dolan Eimear B.156ORCID,Roche Ellen T.347ORCID,Duffy Garry P.125ORCID

Affiliation:

1. Anatomy and Regenerative Medicine Institute (REMEDI), School of Medicine, University of Galway, Galway, Ireland.

2. SFI Centre for Advanced Materials and BioEngineering Research (AMBER), Trinity College Dublin, Dublin, Ireland.

3. Harvard-MIT Program in Health Sciences and Technology, Cambridge, MA, USA.

4. Institute for Medical Engineering and Science, Massachusetts Institute of Technology, Cambridge, MA, USA.

5. CÚRAM, Centre for Research in Medical Devices, University of Galway, Galway, Ireland.

6. Biomedical Engineering, School of Engineering, University of Galway, Galway, Ireland.

7. Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.

8. School of Mathematical and Statistical Sciences, University of Galway, Galway, Ireland.

Abstract

The foreign body response impedes the function and longevity of implantable drug delivery devices. As a dense fibrotic capsule forms, integration of the device with the host tissue becomes compromised, ultimately resulting in device seclusion and treatment failure. We present FibroSensing Dynamic Soft Reservoir (FSDSR), an implantable drug delivery device capable of monitoring fibrotic capsule formation and overcoming its effects via soft robotic actuations. Occlusion of the FSDSR porous membrane was monitored over 7 days in a rodent model using electrochemical impedance spectroscopy. The electrical resistance of the fibrotic capsule correlated to its increase in thickness and volume. Our FibroSensing membrane showed great sensitivity in detecting changes at the abiotic/biotic interface, such as collagen deposition and myofibroblast proliferation. The potential of the FSDSR to overcome fibrotic capsule formation and maintain constant drug dosing over time was demonstrated in silico and in vitro. Controlled closed loop release of methylene blue into agarose gels (with a comparable fold change in permeability relating to 7 and 28 days in vivo) was achieved by adjusting the magnitude and frequency of pneumatic actuations after impedance measurements by the FibroSensing membrane. By sensing fibrotic capsule formation in vivo, the FSDSR will be capable of probing and adapting to the foreign body response through dynamic actuation changes. Informed by real-time sensor signals, this device offers the potential for long-term efficacy and sustained drug dosing, even in the setting of fibrotic capsule formation.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Artificial Intelligence,Control and Optimization,Computer Science Applications,Mechanical Engineering

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