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dc.contributor.authorChen, Wei
dc.contributor.authorWainer, Jacob
dc.contributor.authorRyoo, Si Won
dc.contributor.authorQi, Xiaoyue
dc.contributor.authorChang, Rong
dc.contributor.authorLi, Jason
dc.contributor.authorLee, Seung Ho
dc.contributor.authorMin, Seokkee
dc.contributor.authorWentworth, Adam
dc.contributor.authorCollins, Joy E.
dc.contributor.authorTamang, Siddartha
dc.contributor.authorIshida, Keiko
dc.contributor.authorHayward, Alison
dc.contributor.authorLanger, Robert
dc.contributor.authorTraverso, Giovanni
dc.date.accessioned2024-05-23T19:24:12Z
dc.date.available2024-05-23T19:24:12Z
dc.date.issued2022-01-07
dc.identifier.issn2375-2548
dc.identifier.urihttps://hdl.handle.net/1721.1/155046
dc.description.abstractOral drug administration remains the preferred route for patients and health care providers. Delivery of macromolecules through this route remains challenging because of limitations imposed by the transport across the gastrointestinal epithelium and the dynamic and degradative environment. Here, we present the development of a delivery system that combines physical (microneedle) and nonphysical (enhancer) modes of drug delivery enhancement for a macromolecule in a large animal model. Inspired by the thorny-headed intestinal worm, we report a dynamic omnidirectional mucoadhesive microneedle system capable of prolonged gastric mucosa fixation. Moreover, we incorporate sodium N-[8-(2-hydroxybenzoyl) amino] caprylate along with semaglutide and demonstrate enhanced absorption in swine resistant to physical displacement in the gastric cavity. Meanwhile, we developed a targeted capsule system capable of deploying intact microneedle-containing systems. These systems stand to enable the delivery of a range of drugs through the generation and maintenance of a privileged region in the gastrointestinal tract.en_US
dc.language.isoen
dc.publisherAmerican Association for the Advancement of Scienceen_US
dc.relation.isversionof10.1126/sciadv.abk1792en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceAmerican Association for the Advancement of Scienceen_US
dc.titleDynamic omnidirectional adhesive microneedle system for oral macromolecular drug deliveryen_US
dc.typeArticleen_US
dc.identifier.citationWei Chen et al. ,Dynamic omnidirectional adhesive microneedle system for oral macromolecular drug delivery.Sci. Adv.8,eabk1792(2022).en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineering
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MIT
dc.contributor.departmentMassachusetts Institute of Technology. Division of Comparative Medicine
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineering
dc.relation.journalScience Advancesen_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.updated2024-05-23T19:15:21Z
dspace.orderedauthorsChen, W; Wainer, J; Ryoo, SW; Qi, X; Chang, R; Li, J; Lee, SH; Min, S; Wentworth, A; Collins, JE; Tamang, S; Ishida, K; Hayward, A; Langer, R; Traverso, Gen_US
dspace.date.submission2024-05-23T19:15:25Z
mit.journal.volume8en_US
mit.journal.issue1en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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