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dc.contributor.authorPaletta, Joseph T.
dc.contributor.authorZhang, Hui
dc.contributor.authorBoska, Michael D.
dc.contributor.authorOttaviani, M. Francesca
dc.contributor.authorRajca, Andrzej
dc.contributor.authorNguyen, Hung VanThanh
dc.contributor.authorChen, Qixian
dc.contributor.authorHarvey, Peter
dc.contributor.authorJiang, Yivan
dc.contributor.authorJasanoff, Alan Pradip
dc.contributor.authorJohnson, Jeremiah A.
dc.date.accessioned2018-01-29T18:42:35Z
dc.date.available2018-01-29T18:42:35Z
dc.date.issued2017-07
dc.date.submitted2017-06
dc.identifier.issn2374-7943
dc.identifier.issn2374-7951
dc.identifier.urihttp://hdl.handle.net/1721.1/113328
dc.description.abstractMetal-free magnetic resonance imaging (MRI) agents could overcome the established toxicity associated with metal-based agents in some patient populations and enable new modes of functional MRI in vivo. Herein, we report nitroxide-functionalized brush-arm star polymer organic radical contrast agents (BASP-ORCAs) that overcome the low contrast and poor in vivo stability associated with nitroxide-based MRI contrast agents. As a consequence of their unique nanoarchitectures, BASP-ORCAs possess per-nitroxide transverse relaxivities up to ∼44-fold greater than common nitroxides, exceptional stability in highly reducing environments, and low toxicity. These features combine to provide for accumulation of a sufficient concentration of BASP-ORCA in murine subcutaneous tumors up to 20 h following systemic administration such that MRI contrast on par with metal-based agents is observed. BASP-ORCAs are, to our knowledge, the first nitroxide MRI contrast agents capable of tumor imaging over long time periods using clinical high-field ¹H MRI techniques.en_US
dc.description.sponsorshipNational Institute of Biomedical Imaging and Bioengineering (U.S.) (Grant 1R21EB018529-01A1)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant U01-NS090451)en_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ACSCENTSCI.7B00253en_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.sourceACSen_US
dc.titleNitroxide-Based Macromolecular Contrast Agents with Unprecedented Transverse Relaxivity and Stability for Magnetic Resonance Imaging of Tumorsen_US
dc.typeArticleen_US
dc.identifier.citationNguyen, Hung V.-T. et al. “Nitroxide-Based Macromolecular Contrast Agents with Unprecedented Transverse Relaxivity and Stability for Magnetic Resonance Imaging of Tumors.” ACS Central Science 3, 7 (July 2017): 800–811 © 2017 American Chemical Societyen_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 Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Laboratory for Nuclear Scienceen_US
dc.contributor.mitauthorNguyen, Hung VanThanh
dc.contributor.mitauthorChen, Qixian
dc.contributor.mitauthorHarvey, Peter
dc.contributor.mitauthorJiang, Yivan
dc.contributor.mitauthorJasanoff, Alan Pradip
dc.contributor.mitauthorJohnson, Jeremiah A.
dc.relation.journalACS Central Scienceen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-01-29T17:46:02Z
dspace.orderedauthorsNguyen, Hung V.-T.; Chen, Qixian; Paletta, Joseph T.; Harvey, Peter; Jiang, Yivan; Zhang, Hui; Boska, Michael D.; Ottaviani, M. Francesca; Jasanoff, Alan; Rajca, Andrzej; Johnson, Jeremiah A.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-6945-4057
dc.identifier.orcidhttps://orcid.org/0000-0002-8163-7059
dc.identifier.orcidhttps://orcid.org/0000-0002-2834-6359
dc.identifier.orcidhttps://orcid.org/0000-0001-9157-6491
mit.licensePUBLISHER_POLICYen_US


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