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dc.contributor.author Kim, Eunjoo -
dc.contributor.author Kim, Joon Mee -
dc.contributor.author Kim, Lucia -
dc.contributor.author Choi, Suk Jin -
dc.contributor.author Park, In Suh -
dc.contributor.author Han, Jee Young -
dc.contributor.author Chu, Young Chae -
dc.contributor.author Choi, Eun Sook -
dc.contributor.author Na, Kun -
dc.contributor.author Hong, Soon-Sun -
dc.date.available 2017-07-05T08:47:20Z -
dc.date.created 2017-04-10 -
dc.date.issued 2016-09 -
dc.identifier.issn 1176-9114 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/2308 -
dc.description.abstract In recent years, iron oxide nanoparticles (IONPs) have been applied widely to biomedical fields. However, the relationship between the physicochemical properties of IONPs and their biological behavior is not fully understood yet. We prepared 3-methacryl-oxypropyltrimethoxysilane (MPS)-coated IONPs, which have a neutral hydrophobic surface, and compared their biological behavior to that of Resovist (ferucarbotran), a commercialized IONP formulation modified with carboxymethyl dextran. The rate of MPS-IONP uptake by human aortic endothelial cells (HAoECs) was higher than ferucarbotran uptake, indicating that the neutral hydrophobic nature of MPS-IONPs allowed them to be absorbed more readily through the plasma membrane. However, the signaling pathways activated by MPS-IONPs and ferucarbotran were comparable, suggesting that surface charge is not a key factor for inducing changes in HAoECs. In vivo fate analysis showed that MPS-IONPs accumulated for longer periods in tissues than hydrophilic ferucarbotran. These findings could enlarge our understanding of NP behavior for advanced applications in the biomedical field. -
dc.language English -
dc.publisher Dove Medical Press Ltd -
dc.title The effect of neutral-surface iron oxide nanopar-ticles on cellular uptake and signaling pathways -
dc.type Article -
dc.identifier.doi 10.2147/IJN.S110332 -
dc.identifier.scopusid 2-s2.0-84988864255 -
dc.identifier.bibliographicCitation International Journal of Nanomedicine, v.11, pp.4595 - 4607 -
dc.description.isOpenAccess TRUE -
dc.subject.keywordAuthor iron oxide nanoparticles -
dc.subject.keywordAuthor neutral hydrophobic surface -
dc.subject.keywordAuthor signaling pathway -
dc.subject.keywordAuthor uptake -
dc.subject.keywordAuthor accumulation -
dc.subject.keywordAuthor reactive oxygen species (ROS) -
dc.subject.keywordPlus ACCUMULATION -
dc.subject.keywordPlus ACTIVATION -
dc.subject.keywordPlus CANCER-CELLS -
dc.subject.keywordPlus CHARGE -
dc.subject.keywordPlus Dendrimers -
dc.subject.keywordPlus EXPRESSION -
dc.subject.keywordPlus INTERNALIZATION -
dc.subject.keywordPlus Iron Oxide Nanoparticles -
dc.subject.keywordPlus LARGE GENE LISTS -
dc.subject.keywordPlus LUNG -
dc.subject.keywordPlus Magnetic Nanoparticles -
dc.subject.keywordPlus Neutral Hydrophobic Surface -
dc.subject.keywordPlus OXIDATIVE STRESS -
dc.subject.keywordPlus Reactive Oxygen Species (ROS) -
dc.subject.keywordPlus SIGNALING PATHWAY -
dc.subject.keywordPlus Uptake -
dc.citation.endPage 4607 -
dc.citation.startPage 4595 -
dc.citation.title International Journal of Nanomedicine -
dc.citation.volume 11 -
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Division of Electronics & Information System 1. Journal Articles

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