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dc.contributor.authorCastillo, Betzaida
dc.contributor.authorBadillo, Valerie
dc.contributor.authorHatton, T. Alan
dc.contributor.authorBarletta, Gabriel
dc.contributor.authorBromberg, Lev E.
dc.contributor.authorLopez, Xaira
dc.contributor.authorGonzalez Feliciano, Jose A.
dc.contributor.authorGonzalez, Carlos I.
dc.date.accessioned2013-06-17T13:32:33Z
dc.date.available2013-06-17T13:32:33Z
dc.date.issued2012
dc.date.submitted2012-07
dc.identifier.issn2090-3014
dc.identifier.issn2090-3022
dc.identifier.urihttp://hdl.handle.net/1721.1/79115
dc.description.abstractThe siRNA transfection efficiency of nanoparticles (NPs), composed of a superparamagnetic iron oxide core modified with polycationic polymers (poly(hexamethylene biguanide) or branched polyethyleneimine), were studied in CHO-K1 and HeLa cell lines. Both NPs demonstrated to be good siRNA transfection vehicles, but unmodified branched polyethyleneimine (25 kD) was superior on both cell lines. However, application of an external magnetic field during transfection (magnetofection) increased the efficiency of the superparamagnetic NPs. Furthermore, our results reveal that these NPs are less toxic towards CHO-K1 cell lines than the unmodified polycationic-branched polyethyleneimine (PEI). In general, the external magnetic field did not alter the cell’s viability nor it disrupted the cell membranes, except for the poly(hexamethylene biguanide)-modified NP, where it was observed that in CHO-K1 cells application of the external magnetic field promoted membrane damage. This paper presents new polycationic superparamagnetic NPs as promising transfection vehicles for siRNA and demonstrates the advantages of magnetofection.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant NIH IMBRE P20 RR016470)en_US
dc.description.sponsorship(Grant S06 GM-08216)en_US
dc.publisherHindawi Publishing Corporationen_US
dc.relation.isversionofhttp://dx.doi.org/10.1155/2012/218940en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.0en_US
dc.sourceHindawi Publishing Corporationen_US
dc.titleIntracellular Delivery of siRNA by Polycationic Superparamagnetic Nanoparticlesen_US
dc.typeArticleen_US
dc.identifier.citationCastillo, Betzaida, Lev Bromberg, Xaira López, et al. Intracellular Delivery of siRNA by Polycationic Superparamagnetic Nanoparticles. Journal of Drug Delivery 2012: 1–12. 2012.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.mitauthorBromberg, Lev E.en_US
dc.contributor.mitauthorHatton, T. Alanen_US
dc.relation.journalJournal of Drug Deliveryen_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.updated2013-06-13T11:41:56Z
dc.language.rfc3066en
dc.rights.holderCopyright © 2012 Betzaida Castillo et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dspace.orderedauthorsCastillo, Betzaida; Bromberg, Lev; López, Xaira; Badillo, Valerie; González Feliciano, Jose A.; González, Carlos I.; Hatton, T. Alan; Barletta, Gabrielen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-4558-245X
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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