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김홍태

Kim, Hongtae
Cancer/DNA damage Lab.
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dc.citation.endPage 677 -
dc.citation.number 7 -
dc.citation.startPage 670 -
dc.citation.title MACROMOLECULAR RESEARCH -
dc.citation.volume 23 -
dc.contributor.author Lee, Min Sang -
dc.contributor.author Kim, Nak Won -
dc.contributor.author Lee, Jung Eun -
dc.contributor.author Lim, Dong Woo -
dc.contributor.author Suh, Wonhee -
dc.contributor.author Kim, Hong Tae -
dc.contributor.author Park, Ji Won -
dc.contributor.author Jeong, Ji Hoon -
dc.date.accessioned 2023-12-22T01:07:01Z -
dc.date.available 2023-12-22T01:07:01Z -
dc.date.created 2018-09-19 -
dc.date.issued 2015-07 -
dc.description.abstract Successful cellular delivery of synthetic siRNA depends mainly on the capability of a carrier to form a stable complex with siRNA, which can provide efficient protection of the siRNA from enzyme-mediated degradation and improved cellular uptake. However, due to its short length and rigid structure, cellular delivery of siRNA is often not as efficient as that of plasmid DNA using conventional cationic polymer- and lipid-based carriers. Herein, we synthesized a dendritic gold nanoparticle (Au@MC)-based siRNA delivery system, which provides efficient protection of siRNA and improved cellular uptake. The Au@MC can be readily synthesized from a block copolymer micelle template with a dendritic structure. Au@MC can efficiently form a stable complex with the short and rigid siRNA by localizing it in the space between the branches of the Au@MC. The stability and cellular uptake efficiency were significantly influenced by the structural features of Au@MC, such as size, surface charge, and gap width between the branches. A selected Au@MC/siRNA formulation could successfully achieve highly efficient siRNA transfection in the absence and presence of serum proteins without significant cell toxicity, suggesting the formulation as a potential candidate for siRNA-based clinical gene therapy. -
dc.identifier.bibliographicCitation MACROMOLECULAR RESEARCH, v.23, no.7, pp.670 - 677 -
dc.identifier.doi 10.1007/s13233-015-3091-4 -
dc.identifier.issn 1598-5032 -
dc.identifier.scopusid 2-s2.0-84938864342 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/24886 -
dc.identifier.url https://link.springer.com/article/10.1007%2Fs13233-015-3091-4 -
dc.identifier.wosid 000358667300010 -
dc.language 영어 -
dc.publisher SPRINGER -
dc.title Micelle-templated dendritic gold nanoparticles for enhanced cellular delivery of siRNA -
dc.type Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor non-viral gene delivery -
dc.subject.keywordAuthor siRNA -
dc.subject.keywordAuthor dendritic gold nanoparticles -
dc.subject.keywordAuthor micelle-template synthesis -
dc.subject.keywordPlus GENE DELIVERY -
dc.subject.keywordPlus METAL NANOPARTICLES -
dc.subject.keywordPlus ENVIRONMENT -
dc.subject.keywordPlus DRUGS -
dc.subject.keywordPlus SHAPE -
dc.subject.keywordPlus ACID -
dc.subject.keywordPlus RNA -

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