Issue 4, 2025

Biocompatible PMAO-coated Gd2O3/Fe3O4 composite nanoparticles as an effective T1–T2 dual-mode contrast agent for magnetic resonance imaging

Abstract

In this study, we developed novel Gd2O3/Fe3O4 composite nanoparticles (GFO CNPs) via a simple one-step thermal decomposition of Fe(III) actylacetonate and Gd(III) acetate in octadecene solvent, with oleic acid (OA) and oleylamine (OM) serving as surfactants. The effects of the Gd/Fe molar ratio on the formation, size, and T1, T2 relaxation efficiency of the NPs were investigated. The as-synthesised GFO CNPs were characterised using various analytical techniques such as TEM, HRTEM, XRD, UV-Vis, VSM, EDX and XPS. The results showed that GFO CNPs synthesised at a Gd/Fe ratio of 7/3 (GFO-7/3 CNPs) had an average size of about 10 nm, exhibited monodispersity with a narrow size distribution, and demonstrated superparamagnetic properties at room temperature. Additionally, surface modification of the NPs with PMAO improved their dispersibility and stability in aqueous media. Cytotoxicity tests confirmed the biocompatibility of the PMAO encapsulated GFO CNPs. In vitro relaxivity studies showed high r1 and r2 values of 18.20 and 94.75 mM−1 s−1, respectively, with an r2/r1 ratio of 5.21, outperforming commercial products such as Feraheme, Resovist, Feridex, and Dotarem. These findings suggest that GFO CNPs provide a promising nanoplatform for non-invasive T1–T2 dual-modality MRI diagnosis.

Graphical abstract: Biocompatible PMAO-coated Gd2O3/Fe3O4 composite nanoparticles as an effective T1–T2 dual-mode contrast agent for magnetic resonance imaging

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Article information

Article type
Paper
Submitted
23 Oct 2024
Accepted
07 Jan 2025
First published
09 Jan 2025
This article is Open Access
Creative Commons BY-NC license

Mater. Adv., 2025,6, 1319-1329

Biocompatible PMAO-coated Gd2O3/Fe3O4 composite nanoparticles as an effective T1–T2 dual-mode contrast agent for magnetic resonance imaging

L. T. T. Tam, N. T. N. Linh, L. T. Tam, D. V. Thiet, P. H. Nam, N. T. H. Hoa, L. A. Tuan, N. T. Dung and L. T. Lu, Mater. Adv., 2025, 6, 1319 DOI: 10.1039/D4MA01067A

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