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Exceedingly small iron oxide nanoparticles as positive MRI contrast agents.

Authors :
Wei H
Bruns OT
Kaul MG
Hansen EC
Barch M
Wiśniowska A
Chen O
Chen Y
Li N
Okada S
Cordero JM
Heine M
Farrar CT
Montana DM
Adam G
Ittrich H
Jasanoff A
Nielsen P
Bawendi MG
Source :
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2017 Feb 28; Vol. 114 (9), pp. 2325-2330. Date of Electronic Publication: 2017 Feb 13.
Publication Year :
2017

Abstract

Medical imaging is routine in the diagnosis and staging of a wide range of medical conditions. In particular, magnetic resonance imaging (MRI) is critical for visualizing soft tissue and organs, with over 60 million MRI procedures performed each year worldwide. About one-third of these procedures are contrast-enhanced MRI, and gadolinium-based contrast agents (GBCAs) are the mainstream MRI contrast agents used in the clinic. GBCAs have shown efficacy and are safe to use with most patients; however, some GBCAs have a small risk of adverse effects, including nephrogenic systemic fibrosis (NSF), the untreatable condition recently linked to gadolinium (Gd) exposure during MRI with contrast. In addition, Gd deposition in the human brain has been reported following contrast, and this is now under investigation by the US Food and Drug Administration (FDA). To address a perceived need for a Gd-free contrast agent with pharmacokinetic and imaging properties comparable to GBCAs, we have designed and developed zwitterion-coated exceedingly small superparamagnetic iron oxide nanoparticles (ZES-SPIONs) consisting of ∼3-nm inorganic cores and ∼1-nm ultrathin hydrophilic shell. These ZES-SPIONs are free of Gd and show a high T <subscript>1</subscript> contrast power. We demonstrate the potential of ZES-SPIONs in preclinical MRI and magnetic resonance angiography.

Details

Language :
English
ISSN :
1091-6490
Volume :
114
Issue :
9
Database :
MEDLINE
Journal :
Proceedings of the National Academy of Sciences of the United States of America
Publication Type :
Academic Journal
Accession number :
28193901
Full Text :
https://doi.org/10.1073/pnas.1620145114