Gene silencing efficiency of siRNA-PEG conjugates: Effect of PEGylation site and PEG molecular weight

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dc.contributor.authorJung, Soo-Yeonko
dc.contributor.authorLee, Soo-Hyeonko
dc.contributor.authorMok, Hye-Jungko
dc.contributor.authorChung, Hyun-Jungko
dc.contributor.authorPark, Tae-Gwanko
dc.date.accessioned2013-03-12T01:47:09Z-
dc.date.available2013-03-12T01:47:09Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2010-06-
dc.identifier.citationJOURNAL OF CONTROLLED RELEASE, v.144, no.3, pp.306 - 313-
dc.identifier.issn0168-3659-
dc.identifier.urihttp://hdl.handle.net/10203/101001-
dc.description.abstractSmall interfering RNA (siRNA) was conjugated with poly(ethylene glycol) (PEG) at four different terminal ends (sense 3', sense 5', antisense 3', and antisense 5') via cleavable disulfide and noncleavable thioether linkages to evaluate their gene silencing efficiencies upon complexation with Lipofectamine (TM) 2000. The PEGylation site at the four siRNA termini and PEG molecular weight were not critical factors to significantly affect gene silencing activities. Cleavable siRNA-PEG conjugates showed comparable gene silencing activities to naked siRNA, and exhibited sequence-specific degradation of a target mRNA. Interestingly, noncleavable siRNA-PEG conjugates were processed by Dicer, enabling to exert RNAi effect without showing a target sequence-specific manner. However, only cleavable siRNA-PEG conjugates significantly reduced the extent of INF-alpha release as compared to noncleavable siRNA-PEG conjugates, suggesting that they can be potentially used for therapeutic siRNA applications. (C) 2010 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectSMALL INTERFERING RNA-
dc.subjectPOLYELECTROLYTE COMPLEX MICELLES-
dc.subjectIN-VIVO DELIVERY-
dc.subjectMAMMALIAN-CELLS-
dc.subjectVEGF SIRNA-
dc.subjectPERIPHERAL-BLOOD-
dc.subjectIMMUNE-RESPONSES-
dc.subjectINNATE IMMUNITY-
dc.subjectCELLULAR UPTAKE-
dc.subjectEXPRESSION-
dc.titleGene silencing efficiency of siRNA-PEG conjugates: Effect of PEGylation site and PEG molecular weight-
dc.typeArticle-
dc.identifier.wosid000279089200006-
dc.identifier.scopusid2-s2.0-77953287100-
dc.type.rimsART-
dc.citation.volume144-
dc.citation.issue3-
dc.citation.beginningpage306-
dc.citation.endingpage313-
dc.citation.publicationnameJOURNAL OF CONTROLLED RELEASE-
dc.identifier.doi10.1016/j.jconrel.2010.03.002-
dc.contributor.localauthorChung, Hyun-Jung-
dc.contributor.localauthorPark, Tae-Gwan-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorsiRNA-
dc.subject.keywordAuthorPEGylation-
dc.subject.keywordAuthorCleavable linkage-
dc.subject.keywordAuthorConjugate site-
dc.subject.keywordAuthorGene inhibition-
dc.subject.keywordPlusSMALL INTERFERING RNA-
dc.subject.keywordPlusPOLYELECTROLYTE COMPLEX MICELLES-
dc.subject.keywordPlusIN-VIVO DELIVERY-
dc.subject.keywordPlusMAMMALIAN-CELLS-
dc.subject.keywordPlusVEGF SIRNA-
dc.subject.keywordPlusPERIPHERAL-BLOOD-
dc.subject.keywordPlusIMMUNE-RESPONSES-
dc.subject.keywordPlusINNATE IMMUNITY-
dc.subject.keywordPlusCELLULAR UPTAKE-
dc.subject.keywordPlusEXPRESSION-
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