Imidazolized magnetic nanovectors with endosome disrupting moieties for the intracellular delivery and imaging of siRNA

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dc.contributor.authorE Kim-
dc.contributor.authorH Lee-
dc.contributor.authorY An-
dc.contributor.authorE Jang-
dc.contributor.authorEun Kyung Lim-
dc.contributor.authorB Kang-
dc.contributor.authorJ S Suh-
dc.contributor.authorY M Huh-
dc.contributor.authorS Haam-
dc.date.accessioned2017-04-19T09:58:50Z-
dc.date.available2017-04-19T09:58:50Z-
dc.date.issued2014-
dc.identifier.issn2050-7488-
dc.identifier.uri10.1039/c4tb01274gko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/12299-
dc.description.abstractThe development of a synchronized delivery and imaging system for small interfering RNA (siRNA) is required for the clinical application of RNA interference (RNAi) in cancer treatment. Herein, we report a pH-responsive, magnetic nanoparticle-based siRNA delivery system that can facilitate the safe and efficient delivery and visualization of therapeutic siRNA by high-resolution magnetic resonance (MR) imaging. Cationic poly-l-lysine-graft-imidazole (PLI) with a reactive silane moiety was stably immobilized onto the surface of the assembled manganese ferrite nanoparticles (MFs) through an emulsion process, ensuring high water solubility, enhanced MR contrast effect, and endosome-disrupting functionality. The synthesized nanovectors were then complexed with siRNA targeting the CD44 gene via electrostatic interactions to verify the specific gene-silencing effect. The imidazolized magnetic nanovector (ImMNV) architectures developed here facilitated improved cellular internalization and exhibited a high level in vitro downregulation compared to non-imidazolized MNVs in metastatic breast cancer cells.-
dc.publisherRoyal Soc Chem-
dc.titleImidazolized magnetic nanovectors with endosome disrupting moieties for the intracellular delivery and imaging of siRNA-
dc.title.alternativeImidazolized magnetic nanovectors with endosome disrupting moieties for the intracellular delivery and imaging of siRNA-
dc.typeArticle-
dc.citation.titleJournal of Materials Chemistry A-
dc.citation.number48-
dc.citation.endPage8575-
dc.citation.startPage8566-
dc.citation.volume2-
dc.contributor.affiliatedAuthorEun Kyung Lim-
dc.contributor.alternativeName김은정-
dc.contributor.alternativeName이훈재-
dc.contributor.alternativeName안용희-
dc.contributor.alternativeName장은지-
dc.contributor.alternativeName임은경-
dc.contributor.alternativeName강병훈-
dc.contributor.alternativeName서진석-
dc.contributor.alternativeName허용민-
dc.contributor.alternativeName함승주-
dc.identifier.bibliographicCitationJournal of Materials Chemistry A, vol. 2, no. 48, pp. 8566-8575-
dc.identifier.doi10.1039/c4tb01274g-
dc.description.journalClassY-
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Division of Research on National Challenges > Bionanotechnology Research Center > 1. Journal Articles
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