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dc.contributor.authorCastleberry, Steven A
dc.contributor.authorQuadir, Mohiuddin Abdul
dc.contributor.authorSharkh, Malak Abu
dc.contributor.authorShopsowitz, Kevin
dc.contributor.authorHammond, Paula T
dc.date.accessioned2019-11-11T18:47:11Z
dc.date.available2019-11-11T18:47:11Z
dc.date.issued2017-07
dc.date.submitted2017-03
dc.identifier.issn0168-3659
dc.identifier.urihttps://hdl.handle.net/1721.1/122818
dc.description.abstractAll-trans retinoic acid (ATRA), a derivative of vitamin A, is a common component in cosmetics and commercial acne creams as well as being a first-line chemotherapeutic agent. Today, formulations for the topical application of ATRA rely on creams and emulsions to incorporate the highly hydrophobic ATRA drug. These strategies, when applied to the skin, deliver ATRA as a single bolus, which is immediately taken up into the skin and contributes to many of the known adverse side effects of ATRA treatment, including skin irritation and hair loss. Herein we present a new concept in topical delivery of retinoids by covalently bonding the drug through a hydrolytically degradable ester linkage to a common hydrophilic polymer, polyvinyl alcohol (PVA), creating an amphiphilic nanomaterial that is water-soluble. This PVA bound ATRA can then act as a pro-drug and accumulate within the skin to allow for the sustained controlled delivery of active ATRA. This approach was demonstrated to release active ATRA out to 10 days in vitro while significantly enhancing dermal accumulation of the ATRA in explant pig skin. In vivo we demonstrate that the pro-drug formulation reduces application site inflammation compared to free ATRA and retains the drug at the application site at measurable quantities for up to six days. Keywords: all-trans retinoic acid; poly (vinyl alcohol); polymer conjugate; transdermal drug deliveryen_US
dc.description.sponsorshipUnited States. Army Research Office (Contract W911NF-07-D-0004)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.) (Grant 2P30CA014051-39)en_US
dc.language.isoen
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.jconrel.2017.07.003en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titlePolymer conjugated retinoids for controlled transdermal deliveryen_US
dc.typeArticleen_US
dc.identifier.citationCastleberry, Steven A. "Polymer conjugated retinoids for controlled transdermal delivery." Journal of Controlled Release 262 (September 28, 2017): 1-9 © 2017 Publisheren_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Soldier Nanotechnologiesen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.relation.journalJournal of Controlled Releaseen_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.updated2019-08-20T17:36:31Z
dspace.date.submission2019-08-20T17:36:32Z
mit.journal.volume262en_US


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