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dc.contributor.authorLee, Jong Bum
dc.contributor.authorHong, Jinkee
dc.contributor.authorBonner, Daniel K.
dc.contributor.authorPoon, Zhiyong
dc.contributor.authorHammond, Paula T
dc.date.accessioned2014-11-05T20:45:18Z
dc.date.available2014-11-05T20:45:18Z
dc.date.issued2012-02
dc.date.submitted2011-06
dc.identifier.issn1476-1122
dc.identifier.issn1476-4660
dc.identifier.urihttp://hdl.handle.net/1721.1/91470
dc.description.abstractThe encapsulation and delivery of short interfering RNA (siRNA) has been realized using lipid nanoparticles1, 2, cationic complexes3, 4, inorganic nanoparticles5, 6, 7, 8, RNA nanoparticles9, 10 and dendrimers11. Still, the instability of RNA and the relatively ineffectual encapsulation process of siRNA remain critical issues towards the clinical translation of RNA as a therapeutic1, 12, 13. Here we report the synthesis of a delivery vehicle that combines carrier and cargo: RNA interference (RNAi) polymers that self-assemble into nanoscale pleated sheets of hairpin RNA, which in turn form sponge-like microspheres. The RNAi-microsponges consist entirely of cleavable RNA strands, and are processed by the cell’s RNA machinery to convert the stable hairpin RNA to siRNA only after cellular uptake, thus inherently providing protection for siRNA during delivery and transport to the cytoplasm. More than half a million copies of siRNA can be delivered to a cell with the uptake of a single RNAi-microsponge. The approach could lead to novel therapeutic routes for siRNA delivery.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH) NIBIB Grant R01-EB008082)en_US
dc.description.sponsorshipUnited States. American Recovery and Reinvestment Act of 2009 ((ARRA) grant)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Division of Materials Research Polymers Program grant #0705234)en_US
dc.description.sponsorshipDavid H. Koch Institute for Integrative Cancer Research at MIT (Nanotechnology grant)en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/nmat3253en_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.rights.urien_US
dc.sourcePMCen_US
dc.titleSelf-assembled RNA interference microsponges for efficient siRNA deliveryen_US
dc.typeArticleen_US
dc.identifier.citationLee, Jong Bum, Jinkee Hong, Daniel K. Bonner, Zhiyong Poon, and Paula T. Hammond. “Self-Assembled RNA Interference Microsponges for Efficient siRNA Delivery.” Nature Materials 11, no. 4 (February 26, 2012): 316–322.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineeringen_US
dc.contributor.departmentSingapore-MIT Alliance in Research and Technology (SMART)en_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorLee, Jong Bumen_US
dc.contributor.mitauthorHong, Jinkeeen_US
dc.contributor.mitauthorBonner, Daniel K.en_US
dc.contributor.mitauthorPoon, Zhiyongen_US
dc.contributor.mitauthorHammond, Paula T.en_US
dc.relation.journalNature Materialsen_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
dspace.orderedauthorsLee, Jong Bum; Hong, Jinkee; Bonner, Daniel K.; Poon, Zhiyong; Hammond, Paula T.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-3243-8536
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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