Ferumoxytol nanoparticle uptake in brain during acute neuroinflammation is cell-specific

Abstract Ferumoxytol ultrasmall superparamagnetic iron oxide nanoparticles can enhance contrast between neuroinflamed and normal-appearing brain tissue when used as a contrast agent for high-sensitivity magnetic resonance imaging (MRI). Here we used an anti-dextran antibody (Dx1) that binds the nano...

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Veröffentlicht in:Nanomedicine 2016-08, Vol.12 (6), p.1535-1542
Hauptverfasser: McConnell, Heather L., B.S, Schwartz, Daniel L., B.A, Richardson, Brian E., Ph.D, Woltjer, Randall L., M.D., Ph.D, Muldoon, Leslie L., Ph.D, Neuwelt, Edward A., M.D
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Sprache:eng
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Zusammenfassung:Abstract Ferumoxytol ultrasmall superparamagnetic iron oxide nanoparticles can enhance contrast between neuroinflamed and normal-appearing brain tissue when used as a contrast agent for high-sensitivity magnetic resonance imaging (MRI). Here we used an anti-dextran antibody (Dx1) that binds the nanoparticle's carboxymethyldextran coating to differentiate ferumoxytol from endogenous iron and localize it unequivocally in brain tissue. Intravenous injection of ferumoxytol into immune-competent rats that harbored human tumor xenograft-induced inflammatory brain lesions resulted in heterogeneous and lesion-specific signal enhancement on MRI scans in vivo . We used Dx1 immunolocalization and electron microscopy to identify ferumoxytol in affected tissue post-MRI. We found that ferumoxytol nanoparticles were taken up by astrocyte endfeet surrounding cerebral vessels, astrocyte processes, and CD163+ /CD68+ macrophages, but not by tumor cells. These results provide a biological basis for the delayed imaging changes seen with ferumoxytol and indicate that ferumoxytol-MRI can be used to assess the inflammatory component of brain lesions in the clinic.
ISSN:1549-9634
1549-9642
DOI:10.1016/j.nano.2016.03.009