DC Field | Value | Language |
---|---|---|
dc.contributor.author | E Kim | - |
dc.contributor.author | H Lee | - |
dc.contributor.author | Y An | - |
dc.contributor.author | E Jang | - |
dc.contributor.author | Eun Kyung Lim | - |
dc.contributor.author | B Kang | - |
dc.contributor.author | J S Suh | - |
dc.contributor.author | Y M Huh | - |
dc.contributor.author | S Haam | - |
dc.date.accessioned | 2017-04-19T09:58:50Z | - |
dc.date.available | 2017-04-19T09:58:50Z | - |
dc.date.issued | 2014 | - |
dc.identifier.issn | 2050-7488 | - |
dc.identifier.uri | 10.1039/c4tb01274g | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/12299 | - |
dc.description.abstract | The 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.publisher | Royal Soc Chem | - |
dc.title | Imidazolized magnetic nanovectors with endosome disrupting moieties for the intracellular delivery and imaging of siRNA | - |
dc.title.alternative | Imidazolized magnetic nanovectors with endosome disrupting moieties for the intracellular delivery and imaging of siRNA | - |
dc.type | Article | - |
dc.citation.title | Journal of Materials Chemistry A | - |
dc.citation.number | 48 | - |
dc.citation.endPage | 8575 | - |
dc.citation.startPage | 8566 | - |
dc.citation.volume | 2 | - |
dc.contributor.affiliatedAuthor | Eun Kyung Lim | - |
dc.contributor.alternativeName | 김은정 | - |
dc.contributor.alternativeName | 이훈재 | - |
dc.contributor.alternativeName | 안용희 | - |
dc.contributor.alternativeName | 장은지 | - |
dc.contributor.alternativeName | 임은경 | - |
dc.contributor.alternativeName | 강병훈 | - |
dc.contributor.alternativeName | 서진석 | - |
dc.contributor.alternativeName | 허용민 | - |
dc.contributor.alternativeName | 함승주 | - |
dc.identifier.bibliographicCitation | Journal of Materials Chemistry A, vol. 2, no. 48, pp. 8566-8575 | - |
dc.identifier.doi | 10.1039/c4tb01274g | - |
dc.description.journalClass | Y | - |
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