Bridot Jean-Luc, Stanicki Dimitri, Laurent Sophie, Boutry Sébastien, Gossuin Yves, Leclère Philippe, Lazzaroni Roberto, Vander Elst Luce, Muller Robert N
UMONS, Department of General, Organic and Biomedical Chemistry, NMR and Molecular Imaging Laboratory, B-7000, Mons, Belgium.
Contrast Media Mol Imaging. 2013 Nov-Dec;8(6):466-74. doi: 10.1002/cmmi.1552.
Magnetic resonance imaging (MRI) offers the possibility of tracking cells labelled with a contrast agent and evaluating the progress of cell therapies. This requires efficient cell labelling with contrast agents. A basic incubation of cells with iron oxide nanoparticles (NPs) is a common method. This study reports the synthesis at the gram scale of iron oxide nanoparticles as MRI T₂ contrast agents for cell labelling. These NPs are based on small iron oxide cores coated with a thin polysiloxane shell presenting carboxylic acid functions. The iron oxide cores produced have been characterized by transmission electron microscopy, X-ray diffraction, ζ-potential, infrared, photon correlation spectroscopy, atomic force microscopy, magnetometry and relaxometric measurements. These measurements confirmed the expected surface modification by carboxysilane. Carboxylic groups created electrostatic repulsion between NPs when they are deprotonated. Therefore, highly concentrated aqueous solutions of carboxysilane coated iron oxide NPs can be obtained, up to 70% (w/w). These NPs could be used for cell labelling owing to their aggregation and re-dispersion properties. NPs precipitated in Dulbecco's modified Eagle medium induced a rapid association with 3 T6 fibroblast cells and could easily be re-dispersed in phosphate buffer saline solution to obtain properly labelled cells.
磁共振成像(MRI)为追踪用造影剂标记的细胞以及评估细胞治疗进展提供了可能。这需要用造影剂对细胞进行高效标记。细胞与氧化铁纳米颗粒(NPs)进行简单孵育是一种常用方法。本研究报告了作为用于细胞标记的MRI T₂造影剂的氧化铁纳米颗粒的克级合成。这些纳米颗粒基于包覆有呈现羧酸功能的薄聚硅氧烷壳的小氧化铁核。所制备的氧化铁核已通过透射电子显微镜、X射线衍射、ζ电位、红外光谱、光子相关光谱、原子力显微镜、磁强测量和弛豫测量进行了表征。这些测量证实了预期的羧基硅烷表面修饰。当羧基去质子化时,它们在纳米颗粒之间产生静电排斥。因此,可以获得高达70%(w/w)的羧基硅烷包覆氧化铁纳米颗粒的高浓度水溶液。由于其聚集和再分散特性,这些纳米颗粒可用于细胞标记。在杜氏改良 Eagle培养基中沉淀的纳米颗粒能迅速与3T6成纤维细胞结合,并且可以很容易地在磷酸盐缓冲盐溶液中重新分散以获得标记良好的细胞。