Efficient Functional Delivery of siRNA using Mesoporous Silica Nanoparticles with Ultralarge Pores

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dc.contributor.authorNa, Hee-Kyungko
dc.contributor.authorKim, Mi-Heeko
dc.contributor.authorPark, Ki-Hyunko
dc.contributor.authorRyoo, Soo-Ryoonko
dc.contributor.authorLee, Kyung-Eunko
dc.contributor.authorJeon, Hye-Sungko
dc.contributor.authorRyoo, Ryongko
dc.contributor.authorHyeon, Chang-Bongko
dc.contributor.authorMin, Dal-Heeko
dc.date.accessioned2013-03-12T22:01:32Z-
dc.date.available2013-03-12T22:01:32Z-
dc.date.created2012-08-07-
dc.date.created2012-08-07-
dc.date.issued2012-06-
dc.identifier.citationSMALL, v.8, no.11, pp.1752 - 1761-
dc.identifier.issn1613-6810-
dc.identifier.urihttp://hdl.handle.net/10203/103659-
dc.description.abstractAmong various nanoparticles, mesoporous silica nanoparticles (MSNs) have attracted extensive attention for developing efficient drug-delivery systems, mostly due to their high porosity and biocompatibility. However, due to the small pore size, generally below 5 nm in diameter, potential drugs that are loaded into the pore have been limited to small molecules. Herein, a small interfering RNA (siRNA) delivery strategy based on MSNs possessing pores with an average diameter of 23 nm is presented. The siRNA is regarded as a powerful gene therapeutic agent for treatment of a wide range of diseases by enabling post-transcriptional gene silencing, so-called RNA interference. Highly efficient, sequence-specific, and technically very simple target gene knockdown is demonstrated using MSNs with ultralarge pores of size 23 nm in vitro and in vivo without notable cytotoxicity.-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectSMALL INTERFERING RNA-
dc.subjectENDOTHELIAL GROWTH-FACTOR-
dc.subjectGENE-
dc.subjectCELLS-
dc.subjectTHERAPEUTICS-
dc.subjectCANCER-
dc.subjectRESISTANT-
dc.subjectPLANTS-
dc.titleEfficient Functional Delivery of siRNA using Mesoporous Silica Nanoparticles with Ultralarge Pores-
dc.typeArticle-
dc.identifier.wosid000304817700016-
dc.identifier.scopusid2-s2.0-84861880834-
dc.type.rimsART-
dc.citation.volume8-
dc.citation.issue11-
dc.citation.beginningpage1752-
dc.citation.endingpage1761-
dc.citation.publicationnameSMALL-
dc.identifier.doi10.1002/smll.201200028-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorRyoo, Ryong-
dc.contributor.nonIdAuthorKim, Mi-Hee-
dc.contributor.nonIdAuthorPark, Ki-Hyun-
dc.contributor.nonIdAuthorLee, Kyung-Eun-
dc.contributor.nonIdAuthorJeon, Hye-Sung-
dc.contributor.nonIdAuthorHyeon, Chang-Bong-
dc.contributor.nonIdAuthorMin, Dal-Hee-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorcancer therapy-
dc.subject.keywordAuthordrug delivery-
dc.subject.keywordAuthormesoporous materials-
dc.subject.keywordAuthornanoparticles-
dc.subject.keywordAuthorRNA interference-
dc.subject.keywordPlusSMALL INTERFERING RNA-
dc.subject.keywordPlusENDOTHELIAL GROWTH-FACTOR-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusTHERAPEUTICS-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusRESISTANT-
dc.subject.keywordPlusPLANTS-
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