A high relaxivity Gd(III)DOTA-DSPE-based liposomal contrast agent for magnetic resonance imaging

被引:77
作者
Hak, Sjoerd
Sanders, Honorius M. H. F.
Agrawal, Prashant
Langereis, Sander [2 ]
Grull, Holger [2 ]
Keizer, Henk M. [3 ]
Arena, Francesca [4 ,5 ]
Terreno, Enzo [4 ,5 ]
Strijkers, Gustav J.
Nicolay, Klaas [1 ]
机构
[1] Eindhoven Univ Technol, Biomed NMR, Dept Biomed Engn, NL-5600 Eindhoven, Netherlands
[2] Philips Res, Dept Biomol Engn, Eindhoven, Netherlands
[3] SyMO Chem BV, Eindhoven, Netherlands
[4] Univ Turin, Dept Chem, IFM, Turin, Italy
[5] Univ Turin, Mol Imaging Ctr, Turin, Italy
关键词
Molecular imaging; Magnetic resonance imaging; Contrast agent; Liposomes; Gadolinium; Gd(III)DOTA-DSPE; Longitudinal relaxivity; cryo-TEM; Transmetallation; IN-VIVO; MRI; DELIVERY; TRANSMETALATION; NANOPARTICLE; MACROPHAGES; MICELLES; SYSTEM;
D O I
10.1016/j.ejpb.2008.09.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The field of molecular imaging aims to visualize and quantify (patho)physiological processes at the cellular and molecular level. Sensitive and site-targeted contrast agents are employed to visualize molecular constituents of processes of interest. The principal aim of this study was to develop a magnetic resonance imaging (MRI) detectable liposome with high relaxivity and stability. To this end, Gd(III)DOTA-DSPE was synthesized and incorporated in a liposomal formulation. The resulting liposomes were extensively characterized in vitro in terms of contrast agent efficiency and structural properties. The liposomes were shown to have a high longitudinal relaxivity, which is crucial for the detection of low concentration molecular markers in molecular imaging studies. We also demonstrated that Gd(III)DOTA-DSPE exhibits no detectable transmetallation upon incubation with Zn(II). This is important as it significantly contributes to the biocompatibility of the contrast agent. The present liposome preparation will serve as versatile and well characterized platform for molecular imaging and targeted drug delivery studies. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:397 / 404
页数:8
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