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dc.contributor.authorNguyen, Hung VanThanh
dc.contributor.authorZhang, Hui
dc.contributor.authorHarvey, Peter
dc.contributor.authorYan, Changcun
dc.contributor.authorMathieu, Clelia
dc.contributor.authorGolder, Matthew R
dc.contributor.authorJiang, Yivan
dc.contributor.authorOttaviani, Maria Francesca
dc.contributor.authorJasanoff, Alan Pradip
dc.contributor.authorRajca, Andrzej
dc.contributor.authorGhobrial, Irene
dc.contributor.authorGhoroghchian, Paiman Peter
dc.contributor.authorJohnson, Jeremiah A.
dc.date.accessioned2020-01-22T18:11:14Z
dc.date.available2020-01-22T18:11:14Z
dc.date.issued2018-11-02
dc.date.submitted2018-08-13
dc.identifier.issn1936-0851
dc.identifier.issn1936-086X
dc.identifier.urihttps://hdl.handle.net/1721.1/123532
dc.description.abstractNitroxides occupy a privileged position among plausible metal-free magnetic resonance imaging (MRI) contrast agents (CAs) due to their inherently low-toxicity profiles; nevertheless, their translational development has been hindered by a lack of appropriate contrast sensitivity. Nanostructured materials with high nitroxide densities, where each individual nitroxide within a macromolecular construct contributes to the image contrast, could address this limitation, but the synthesis of such materials remains challenging. Here, we report a modular and scalable synthetic approach to nitroxide-based brush-arm star polymer (BASP) organic radical CAs (ORCAs) with high nitroxide loadings. The optimized -30 nm diameter "BASP-ORCA3" displays outstanding T₂ sensitivity with a very high molecular transverse relaxivity (r₂ > 1000 mM⁻¹ s⁻¹). BASP-ORCA3 further exhibits excellent stability in vivo, no acute toxicity, and highly desirable pharmacokinetic and biodistribution profiles for longitudinal detection of tumors by MRI. When injected intravenously into mice bearing subcutaneous plasmacytomas, BASP-ORCA3 affords distinct in vivo visualization of tumors on translationally relevant time scales. Leveraging its high sensitivity, BASP-ORCA3 enables efficient mapping of tumor necrosis, which is an important biomarker to predict therapeutic outcomes. Moreover, BASP-ORCA3 allows for detection of millimetric tumor implants in a disseminated murine model of advanced-stage human ovarian cancer that possess genetic, histological, and vascular characteristics that are similar to those seen in patients. This work establishes BASP-ORCA3 as a promising metal-free spin contrast agent for MRI. Keywords: magnetic resonance imaging; nitroxide; ring-opening metathesis polymerization; star polymers; canceren_US
dc.description.sponsorshipNational Institute of Health (U.S.) (U01-NS090451)en_US
dc.description.sponsorshipNational Institute of Health (U.S.) (1R01CA220468-01)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.) (1R01CA220468-01)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.) (Koch Institute Support Grant P30-CA14051)en_US
dc.language.isoen
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionofhttps://doi.org/10.1021/acsnano.8b06160en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePMCen_US
dc.titleTriply Loaded Nitroxide Brush-Arm Star Polymers Enable Metal-Free Millimetric Tumor Detection by Magnetic Resonance Imagingen_US
dc.typeArticleen_US
dc.identifier.citationNguyen, Hung V.-T. "Triply Loaded Nitroxide Brush-Arm Star Polymers Enable Metal-Free Millimetric Tumor Detection by Magnetic Resonance Imaging." ACS Nano, 12, 11, (November 2018): 11343-11354 © 2018 American Chemical Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Nuclear Science and Engineeringen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.relation.journalACS Nanoen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-12-20T16:47:05Z
dspace.date.submission2019-12-20T16:47:11Z
mit.journal.volume12en_US
mit.journal.issue11en_US
mit.metadata.statusComplete


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