Issue 6, 2018, Issue in Progress

Stable and non-toxic ultrasmall gadolinium oxide nanoparticle colloids (coating material = polyacrylic acid) as high-performance T1 magnetic resonance imaging contrast agents

Abstract

For use as positive (T1) magnetic resonance imaging contrast agents (MRI-CAs), gadolinium oxide (Gd2O3) nanoparticle colloids (i.e. nanoparticles coated with hydrophilic ligands) should be stable, non-toxic, and ultrasmall in particle diameter for renal excretion. In addition, they should have a high longitudinal water proton relaxivity (r1) and r2/r1 ratio that is close to one (r2 = transverse water proton relaxivity) for high-performance. In this study, we report ultrasmall Gd2O3 nanoparticle colloids [coating material = polyacrylic acid, Mw = ∼5100 Da] satisfying these conditions. The particle diameter was monodisperse with an average value of 2.0 ± 0.1 nm. The colloidal suspension exhibited a high r1 value of 31.0 ± 0.1 s−1 mM−1 and r2/r1 ratio of 1.2, where r1 was ∼8 times higher than that of commercial Gd-chelates: the cooperative induction model was proposed to explain this. The effectiveness of the colloidal suspension as a high-performance T1 MRI-CA was confirmed by taking in vivo T1 MR images in a mouse after intravenous administration. Highly positive contrast enhancements were observed in various organs of the mouse such as the liver, kidneys, and bladder. The colloidal suspension was then excreted through the bladder.

Graphical abstract: Stable and non-toxic ultrasmall gadolinium oxide nanoparticle colloids (coating material = polyacrylic acid) as high-performance T1 magnetic resonance imaging contrast agents

Article information

Article type
Paper
Submitted
27 Oct 2017
Accepted
04 Jan 2018
First published
16 Jan 2018
This article is Open Access
Creative Commons BY license

RSC Adv., 2018,8, 3189-3197

Stable and non-toxic ultrasmall gadolinium oxide nanoparticle colloids (coating material = polyacrylic acid) as high-performance T1 magnetic resonance imaging contrast agents

X. Miao, S. L. Ho, T. Tegafaw, H. Cha, Y. Chang, I. T. Oh, A. M. Yaseen, S. Marasini, A. Ghazanfari, H. Yue, K. S. Chae and G. H. Lee, RSC Adv., 2018, 8, 3189 DOI: 10.1039/C7RA11830A

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