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dc.contributor.authorPaolini, Marion
dc.contributor.authorFenton, Owen Shea
dc.contributor.authorBhattacharya, Chandrabali
dc.contributor.authorAndresen, Jason
dc.contributor.authorLanger, Robert S
dc.date.accessioned2020-11-18T20:59:21Z
dc.date.available2020-11-18T20:59:21Z
dc.date.issued2019-04
dc.identifier.issn1387-2176
dc.identifier.issn1572-8781
dc.identifier.urihttps://hdl.handle.net/1721.1/128523
dc.description.abstractDeveloping strategies to deliver the required dose of therapeutics into target tissues and cell populations within the body is a principal aim of controlled release and drug delivery. Specifically, there is an interest in developing formulations that can achieve drug concentrations within the therapeutic window, for extended periods of time, with tunable release profiles, and with minimal complication and distress for the patient. To date, drug delivery systems have been developed to serve as depots, triggers, and carriers for therapeutics including small molecules, biologics, and cell-based therapies. Notably, the efficacy of these systems is intricately tied to the manner in which they are administered. For example, systemic and oral routes of administration are common, but both can result in rapid clearance from the organism. Towards this end, what formulation and administration route strategies are available to prolong the bioavailability of therapeutics? Here, we discuss historical and modern drug delivery systems, with the intention of exploring how properties including formulation, administration route and chemical structure influence the ability to achieve extended-release drug release profiles within the body.en_US
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionofhttps://doi.org/10.1007/s10544-019-0386-9en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceSpringer USen_US
dc.titlePolymers for extended-release administrationen_US
dc.typeArticleen_US
dc.identifier.citationPaolini, Marion S. et al. "Polymers for extended-release administration." Biomedical Microdevices 21, 2 (April 2019): 45 © 2019 Springer Science Business Media, LLCen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.relation.journalBiomedical Microdevicesen_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.updated2020-09-24T21:37:31Z
dc.language.rfc3066en
dc.rights.holderSpringer Science+Business Media, LLC, part of Springer Nature
dspace.embargo.termsY
dspace.date.submission2020-09-24T21:37:31Z
mit.journal.volume21en_US
mit.journal.issue2en_US
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusComplete


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