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dc.contributor.authorAbramson, Alex
dc.contributor.authorCaffarel Salvador, Ester
dc.contributor.authorSoares, Vance
dc.contributor.authorMinahan Jr, Daniel J
dc.contributor.authorTian, Ryan Yu
dc.contributor.authorLu, Xiaoya
dc.contributor.authorDellal, David (David M.)
dc.contributor.authorGao, Yuan
dc.contributor.authorKim, Soyoung
dc.contributor.authorWainer, Jacob P
dc.contributor.authorCollins, Joy E
dc.contributor.authorTamang, Siddartha M
dc.contributor.authorHayward, Alison M
dc.contributor.authorYoshitake, Tadayuki
dc.contributor.authorLee, Hsiang-Chieh
dc.contributor.authorFujimoto, James G
dc.contributor.authorFels, Johannes
dc.contributor.authorFrederiksen, Morten Revsgaard
dc.contributor.authorRahbek, Ulrik
dc.contributor.authorRoxhed, Niclas
dc.contributor.authorLanger, Robert S
dc.contributor.authorTraverso, Carlo Giovanni
dc.date.accessioned2021-01-04T19:42:56Z
dc.date.available2021-01-04T19:42:56Z
dc.date.issued2019-10
dc.date.submitted2018-12
dc.identifier.issn1078-8956
dc.identifier.issn1546-170X
dc.identifier.urihttps://hdl.handle.net/1721.1/128929
dc.description.abstractInsulin and other injectable biologic drugs have transformed the treatment of patients suffering from diabetes1,2, yet patients and healthcare providers often prefer to use and prescribe less effective orally dosed medications3–5. Compared with subcutaneously administered drugs, oral formulations create less patient discomfort4, show greater chemical stability at high temperatures6, and do not generate biohazardous needle waste7. An oral dosage form for biologic medications is ideal; however, macromolecule drugs are not readily absorbed into the bloodstream through the gastrointestinal tract8. We developed an ingestible capsule, termed the luminal unfolding microneedle injector, which allows for the oral delivery of biologic drugs by rapidly propelling dissolvable drug-loaded microneedles into intestinal tissue using a set of unfolding arms. During ex vivo human and in vivo swine studies, the device consistently delivered the microneedles to the tissue without causing complete thickness perforations. Using insulin as a model drug, we showed that, when actuated, the luminal unfolding microneedle injector provided a faster pharmacokinetic uptake profile and a systemic uptake >10% of that of a subcutaneous injection over a 4-h sampling period. With the ability to load a multitude of microneedle formulations, the device can serve as a platform to orally deliver therapeutic doses of macromolecule drugs.en_US
dc.description.sponsorshipNIH (Grant EB-00244)en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/s41591-019-0598-9en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePMCen_US
dc.titleA luminal unfolding microneedle injector for oral delivery of macromoleculesen_US
dc.typeArticleen_US
dc.identifier.citationAbramson, Alex et al. "A luminal unfolding microneedle injector for oral delivery of macromolecules." Nature Medicine 25, 10: 1512–1518 © 2019 The Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Division of Comparative Medicineen_US
dc.contributor.departmentMassachusetts Institute of Technology. Media Laboratoryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Research Laboratory of Electronicsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.relation.journalNature Medicineen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2020-12-14T19:45:04Z
dspace.orderedauthorsAbramson, A; Caffarel-Salvador, E; Soares, V; Minahan, D; Tian, RY; Lu, X; Dellal, D; Gao, Y; Kim, S; Wainer, J; Collins, J; Tamang, S; Hayward, A; Yoshitake, T; Lee, H-C; Fujimoto, J; Fels, J; Frederiksen, MR; Rahbek, U; Roxhed, N; Langer, R; Traverso, Gen_US
dspace.date.submission2020-12-14T19:45:16Z
mit.journal.volume25en_US
mit.journal.issue10en_US
mit.licensePUBLISHER_POLICY
mit.metadata.statusComplete


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