Design, synthesis, and evaluation of gadolinium cationic lipids as tools for biodistribution studies of gene delivery complexes

被引:37
作者
Leclercq, F
Cohen-Ohana, M
Mignet, N
Sbarbati, A
Herscovici, J
Scherman, D
Byk, G
机构
[1] ENSCP, UMR 7001, CNRS, Aventis, F-75231 Paris, France
[2] Bar Ilan Univ, Dept Chem, Lab Peptidomimet & Genet Chem, IL-52900 Ramat Gan, Israel
[3] Univ Verona, Dept MOrphol & Biomed Sci, Sect Anat & Histol, I-37100 Verona, Italy
关键词
D O I
10.1021/bc025567e
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Gadolinium-chelating cationic lipids have been synthesized to obtain lipoplexes with MRI contrast properties. These compounds were designed to follow the biodistribution of synthetic DNA for gene delivery by nuclear magnetic resonance imaging. The lipid MCO-I-68 was synthesized, and chelate complexes with gadolinium were formed and characterized in terms of physicochemical and DNA binding properties. The transfection activity of MCO-I-68-Gd/DNA complexes was assayed in vitro on NIH 3T3. Different formulations of the product were tested. When up to 5% of the gadolinium lipid complexes were co-formulated with the cationic lipid RPR120535 used as a reference, the transfection levels were maintained as compared to RPR120535 alone. To date, only a liposomal formulation of a gadolinium-cationic lipid chelate without DNA had been observed using magnetic resonance imaging. In vivo intratumoral administration of MCO-I-68-Gd/DNA lipoplexes to tumor model led to an important increase of the NMR signal. It was demonstrated that the new complexes also acted as transfection carriers when they were formulated from liposomes.
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收藏
页码:112 / 119
页数:8
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