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Nitroxide-Based Macromolecular Contrast Agents with Unprecedented Transverse Relaxivity and Stability for Magnetic Resonance Imaging of Tumors

Author(s)
Paletta, Joseph T.; Zhang, Hui; Boska, Michael D.; Ottaviani, M. Francesca; Rajca, Andrzej; Nguyen, Hung VanThanh; Chen, Qixian; Harvey, Peter; Jiang, Yivan; Jasanoff, Alan Pradip; Johnson, Jeremiah A.; ... Show more Show less
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Abstract
Metal-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.
Date issued
2017-07
URI
http://hdl.handle.net/1721.1/113328
Department
Massachusetts Institute of Technology. Department of Biological Engineering; Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences; Massachusetts Institute of Technology. Department of Chemistry; Massachusetts Institute of Technology. Laboratory for Nuclear Science
Journal
ACS Central Science
Publisher
American Chemical Society (ACS)
Citation
Nguyen, 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 Society
Version: Final published version
ISSN
2374-7943
2374-7951

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