Literature DB >> 28193901

Exceedingly small iron oxide nanoparticles as positive MRI contrast agents.

He Wei1, Oliver T Bruns1, Michael G Kaul2, Eric C Hansen1, Mariya Barch3, Agata Wiśniowska4, Ou Chen5, Yue Chen1, Nan Li3,6,7, Satoshi Okada3, Jose M Cordero1, Markus Heine8, Christian T Farrar9, Daniel M Montana1,10, Gerhard Adam2, Harald Ittrich2, Alan Jasanoff3,6,7, Peter Nielsen8, Moungi G Bawendi11.   

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 T1 contrast power. We demonstrate the potential of ZES-SPIONs in preclinical MRI and magnetic resonance angiography.

Entities:  

Keywords:  exceedingly small iron oxide nanoparticles; gadolinium-free positive MR contrast agent; preclinical magnetic resonance imaging; renal clearance

Mesh:

Substances:

Year:  2017        PMID: 28193901      PMCID: PMC5338531          DOI: 10.1073/pnas.1620145114

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  45 in total

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