Magnetoliposomes as magnetic resonance imaging contrast agents

被引:64
|
作者
Soenen, Stefaan J. [1 ]
Vande Velde, Greetje [2 ]
Ketkar-Atre, Ashwini [2 ]
Himmelreich, Uwe [2 ]
De Cuyper, Marcel [1 ]
机构
[1] KULeuven, Lab BioNanoColloids, Kortrijk, Belgium
[2] KULeuven, Univ Med Hosp Gasthuisberg, Biomed NMR Unit, MoSAIC, Louvain, Belgium
关键词
IRON-OXIDE PARTICLES; 1,2-DIMYRISTOYL-SN-GLYCERO-3-PHOSPHOCHOLINE DMPC LIPOSOMES; BACTERIAL MAGNETOSOMES; IN-VIVO; SUPERPARAMAGNETIC LIPOSOMES; CATIONIC MAGNETOLIPOSOMES; SURFACE FUNCTIONALIZATION; MEDIATED DELIVERY; LOADED LIPOSOMES; GENE DELIVERY;
D O I
10.1002/wnan.122
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Among the wide variety in iron oxide nanoparticles which are routinely used as magnetic resonance imaging (MRI) contrast agents, magnetoliposomes (MLs) take up a special place. In the present work, the two main types (large and small MLs) are defined and their specific features are commented. For both types of MLs, the flexibility of the lipid coating allows for efficient functionalization, enabling bimodal imaging (e.g., MRI and fluorescence) or the use of MLs as theranostics. These features are especially true for large MLs, where several magnetite cores are encapsulated within a single large liposome, which were found to be highly efficient theranostic agents. By carefully fine-tuning the number of magnetite cores and attaching Gd3+-complexes onto the liposomal surface, the large MLs can be efficiently optimized for dynamic MRI. A special type of MLs, biogenic MLs, can also be efficiently used in this regard, with potential applications in cancer treatment and imaging. Small MLs, where the lipid bilayer is immediately attached onto a solid magnetite core, give a very high r(2)/r(1) ratio. The flexibility of the lipid bilayer allows the incorporation of poly(ethylene glycol)-lipid conjugates to increase blood circulation times and be used as bone marrow contrast agents. Cationic lipids can also be incorporated, leading to high cell uptake and associated strong contrast generation in MRI of implanted cells. Unique for these small MLs is the high resistance the particles exhibit against intracellular degradation compared with dextran-or citrate-coated particles. Additionally, intracellular clustering of the iron oxide cores enhances negative contrast generation and enables longer tracking of labeled cells in time. (C) 2011 John Wiley & Sons, Inc. WIREs Nanomed Nanobiotechnol 2011 3 197-211 DOI:10.1002/wnan.122
引用
收藏
页码:197 / 211
页数:15
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