dc.contributor.author | Luo, X. | |
dc.contributor.author | Wang, Wei | |
dc.contributor.author | Dorkin, Joseph Robert | |
dc.contributor.author | Veiseh, Omid | |
dc.contributor.author | Chang, Pyung-Hun | |
dc.contributor.author | Abutbul-Ionita, I. | |
dc.contributor.author | Danino, D. | |
dc.contributor.author | Langer, Robert S | |
dc.contributor.author | Anderson, Daniel Griffith | |
dc.contributor.author | Dong, Y. | |
dc.date.accessioned | 2019-08-13T15:55:27Z | |
dc.date.available | 2019-08-13T15:55:27Z | |
dc.date.issued | 2017-01 | |
dc.date.submitted | 2016-09 | |
dc.identifier.issn | 2047-4830 | |
dc.identifier.issn | 2047-4849 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/121985 | |
dc.description.abstract | Delivery is the key challenge for siRNA based therapeutics. Here, we report the development of new poly(glycoamidoamine) brush nanomaterials for efficient siRNA delivery. GluN4C10 polymer brush nanoparticles, a lead material, demonstrated significantly improved delivery efficiency for siRNA against factor VII (FVII) in mice compared to poly(glycoamidoamine) brush nanomaterials reported previously. | en_US |
dc.description.sponsorship | National Institutes of Health (U.S.) (Grant R01-EB000244–27) | en_US |
dc.description.sponsorship | National Institutes of Health (U.S.) (Grant 5-R01-CA132091–04) | en_US |
dc.description.sponsorship | National Institutes of Health (U.S.) (Grant R01-DE016516–03) | en_US |
dc.language.iso | en | |
dc.publisher | Royal Society of Chemistry (RSC) | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1039/c6bm00683c | en_US |
dc.rights | Creative Commons Attribution-Noncommercial-Share Alike | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | en_US |
dc.source | PMC | en_US |
dc.title | Poly(glycoamidoamine) brush nanomaterials for systemic siRNA delivery in vivo | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Luo, X. et al. "Poly(glycoamidoamine) brush nanomaterials for systemic siRNA delivery in vivo." Biomaterials Science 1 (January 2017): 38-40 © 2017 The Royal Society of Chemistry | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biology | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Chemical Engineering | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Institute for Medical Engineering & Science | en_US |
dc.contributor.department | Koch Institute for Integrative Cancer Research at MIT | en_US |
dc.relation.journal | Biomaterials Science | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dc.date.updated | 2019-08-09T13:40:38Z | |
dspace.date.submission | 2019-08-09T13:40:38Z | |
mit.journal.volume | 5 | en_US |
mit.journal.issue | 1 | en_US |