| Literature DB >> 34654743 |
He Wei1, Agata Wiśniowska2, Jingxuan Fan1, Peter Harvey1, Yuanyuan Li3, Victoria Wu1, Eric C Hansen4, Juanye Zhang4, Michael G Kaul5, Abigail M Frey1, Gerhard Adam5, Anatoly I Frenkel3,6, Moungi G Bawendi7, Alan Jasanoff8.
Abstract
Magnetic nanoparticles are robust contrast agents for MRI and often produce particularly strong signal changes per particle. Leveraging these effects to probe cellular- and molecular-level phenomena in tissue can, however, be hindered by the large sizes of typical nanoparticle contrast agents. To address this limitation, we introduce single-nanometer iron oxide (SNIO) particles that exhibit superparamagnetic properties in conjunction with hydrodynamic diameters comparable to small, highly diffusible imaging agents. These particles efficiently brighten the signal in T 1-weighted MRI, producing per-molecule longitudinal relaxation enhancements over 10 times greater than conventional gadolinium-based contrast agents. We show that SNIOs permeate biological tissue effectively following injection into brain parenchyma or cerebrospinal fluid. We also demonstrate that SNIOs readily enter the brain following ultrasound-induced blood-brain barrier disruption, emulating the performance of a gadolinium agent and providing a basis for future biomedical applications. These results thus demonstrate a platform for MRI probe development that combines advantages of small-molecule imaging agents with the potency of nanoscale materials.Entities:
Keywords: brain; iron oxide nanoparticle; magnetic resonance imaging; molecular imaging
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Year: 2021 PMID: 34654743 PMCID: PMC8545496 DOI: 10.1073/pnas.2102340118
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205