Key result
Administration of 0.015 and 0.038 mmol Gd/kg of two Gd micelle formulations produced significant vessel wall enhancement in ApoE(-/-) mice, which was not affected by the choice of amphiphile.
Why the study?
Does the choice of amphiphile in Gadolinium mixed-micelles affect in vivo MR efficacy for atherosclerotic plaque imaging in ApoE(-/-) mice?
Does the choice of amphiphile in Gadolinium mixed-micelles affect in vivo MR efficacy for atherosclerotic plaque imaging in ApoE(-/-) mice?
The surface properties of Gadolinium micelles, rather than the specific amphiphile or micelle size, appear to regulate liver uptake and atherosclerotic vessel wall enhancement in ApoE(-/-) mice.
Amphiphile choice does not alter vessel wall enhancement in this model; leaves open whether surface properties drive human plaque imaging.
Gadolinium (Gd) micelles are nanoparticles that incorporate phospholipids, surfactants, and lipophilic Gd complexes. Preliminary studies have shown that lipid-based nanoparticles may penetrate atherosclerotic plaque. The aim of the current study was to prepare, characterize, and evaluate in vivo the efficacy of two Gd micelle formulations using apolipoprotein E knockout (ApoE(-/-)) mouse models of atherosclerosis. Gd micelles were prepared using two different amphiphiles but similar GdDTPA lipids, surfactants, and fluorescent labels. The results indicate that the choice of amphiphile may affect the particle size, relaxivity, and blood clearance in wild-type mice (WT). However, the in vivo MR efficacy, with respect to uptake in the vessel wall of ApoE(-/-) mice, was not affected by the amphiphile used. Significant wall enhancement of ApoE(-/-) mice was observed following administration of 0.015 and 0.038 mmol Gd/kg of both micelle formulations. No significant enhancement of the vessel wall of WT mice was observed for any of the dosages or formulations tested. Additionally, liver uptake 24 hr post-injection (p.i.) was not influenced by the choice of amphiphile. The results of this study strongly suggest that liver uptake and wall enhancement may be regulated by the surface properties of the micelle and not by other factors, such as micelle size.
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Briley‐Sæbø et al. (2006) studied Atherosclerosis. Gadolinium (Gd) mixed-micelles vs. Wild-type mice (WT) / alternative amphiphile formulation was evaluated on In vivo MR efficacy (uptake in the vessel wall) and liver uptake. Administration of 0.015 and 0.038 mmol Gd/kg of two Gd micelle formulations produced significant vessel wall enhancement in ApoE(-/-) mice, which was not affected by the choice of amphiphile.
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