Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/78327
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dc.contributorDepartment of Health Technology and Informaticsen_US
dc.creatorLee, Cen_US
dc.creatorKim, GRen_US
dc.creatorYoon, Jen_US
dc.creatorKim, SEen_US
dc.creatorYoo, JSen_US
dc.creatorPiao, Yen_US
dc.date.accessioned2018-09-28T01:16:13Z-
dc.date.available2018-09-28T01:16:13Z-
dc.identifier.urihttp://hdl.handle.net/10397/78327-
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.rightsOpen Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.en_US
dc.rights© The Author(s) 2018en_US
dc.rightsThe following publication Lee, C., Kim, G. R., Yoon, J., Kim, S. E., Yoo, J. S., & Piao, Y. (2018). In vivo delineation of glioblastoma by targeting tumor-associated macrophages with near-infrared fluorescent silica coated iron oxide nanoparticles in orthotopic xenografts for surgical guidance. Scientific Reports, 8(1), 11122, 1-12 is available at https://doi.org/10.1038/s41598-018-29424-4en_US
dc.titleIn vivo delineation of glioblastoma by targeting tumor-associated macrophages with near-infrared fluorescent silica coated iron oxide nanoparticles in orthotopic xenografts for surgical guidanceen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1en_US
dc.identifier.epage12en_US
dc.identifier.volume8en_US
dc.identifier.doi10.1038/s41598-018-29424-4en_US
dcterms.abstractGlioblastoma multiforme (GBM) is the most aggressive and lethal type of human brain cancer. Surgery is a current gold standard for GBM treatment but the complete surgical resection of GBM is almost impossible due to their diffusive characteristics into surrounded normal brain tissues. There is an urgent need to develop a sensitive imaging tool for accurate delineation of GBM in the operating room to guide surgeons. Here we illustrate the feasibility of using near-infrared fluorescent silica coated iron oxide nanoparticles (NF-SIONs) with high water dispersion capacity and strong fluorescence stability for intraoperative imaging of GBM by targeting tumor-associated macrophages. Abundant macrophage infiltration is a key feature of GBM margins and it is well associated with poor prognosis. We synthesized NF-SIONs of about 37 nm to maximize endocytosis activity for macrophage uptake. The NF-SIONs selectively visualized tumor-associated macrophage populations by in vitro live-cell imaging and in vivo fluorescence imaging. In the orthotopic GBM xenograft models, the NF-SIONs could successfully penetrate blood-brain barrier and delineated tumor burden specifically. Taken together, this study showcased the potential applications in GBM treatment for improved intraoperative staging and more radical surgery as well as dual modality benefit in order to circumvent previous clinical failure.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationScientific reports, 2018, v. 8, 11122, p.1-12en_US
dcterms.isPartOfScientific reportsen_US
dcterms.issued2018-
dc.identifier.isiWOS:000439549800001-
dc.identifier.ros2018001129-
dc.identifier.eissn2045-2322en_US
dc.identifier.artn11122en_US
dc.description.validate201809 bcrcen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera0319-n01, a0621-n02en_US
dc.identifier.SubFormID616-
dc.description.fundingSourceSelf-fundeden_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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