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dc.contributor.authorWhyte, William
dc.contributor.authorGoswami, Debkalpa
dc.contributor.authorWang, Sophie X.
dc.contributor.authorFan, Yiling
dc.contributor.authorWard, Niamh A.
dc.contributor.authorLevey, Ruth E.
dc.contributor.authorBeatty, Rachel
dc.contributor.authorRobinson, Scott T.
dc.contributor.authorSheppard, Declan
dc.contributor.authorO’Connor, Raymond
dc.contributor.authorMonahan, David S.
dc.contributor.authorTrask, Lesley
dc.contributor.authorMendez, Keegan L.
dc.contributor.authorVarela, Claudia E.
dc.contributor.authorHorvath, Markus A.
dc.contributor.authorWylie, Robert
dc.contributor.authorO’Dwyer, Joanne
dc.contributor.authorDomingo-Lopez, Daniel A.
dc.contributor.authorRothman, Arielle S.
dc.contributor.authorDuffy, Garry P.
dc.contributor.authorDolan, Eimear B.
dc.contributor.authorRoche, Ellen T.
dc.date.accessioned2024-04-11T14:35:45Z
dc.date.available2024-04-11T14:35:45Z
dc.date.issued2022-08-03
dc.identifier.issn2041-1723
dc.identifier.urihttps://hdl.handle.net/1721.1/154123
dc.description.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.en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionof10.1038/s41467-022-32147-wen_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceSpringer Natureen_US
dc.subjectGeneral Physics and Astronomyen_US
dc.subjectGeneral Biochemistry, Genetics and Molecular Biologyen_US
dc.subjectGeneral Chemistryen_US
dc.subjectMultidisciplinaryen_US
dc.titleDynamic actuation enhances transport and extends therapeutic lifespan in an implantable drug delivery platformen_US
dc.typeArticleen_US
dc.identifier.citationWhyte, W., Goswami, D., Wang, S.X. et al. Dynamic actuation enhances transport and extends therapeutic lifespan in an implantable drug delivery platform. Nat Commun 13, 4496 (2022).en_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Science
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineering
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technology
dc.relation.journalNature Communicationsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2024-04-11T14:21:08Z
dspace.orderedauthorsWhyte, W; Goswami, D; Wang, SX; Fan, Y; Ward, NA; Levey, RE; Beatty, R; Robinson, ST; Sheppard, D; O’Connor, R; Monahan, DS; Trask, L; Mendez, KL; Varela, CE; Horvath, MA; Wylie, R; O’Dwyer, J; Domingo-Lopez, DA; Rothman, AS; Duffy, GP; Dolan, EB; Roche, ETen_US
dspace.date.submission2024-04-11T14:21:12Z
mit.journal.volume13en_US
mit.journal.issue1en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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