首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Quaternary complexes composed of plasmid DNA/protamine/fish sperm DNA/stearic acid grafted chitosan oligosaccharide micelles for gene delivery
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Quaternary complexes composed of plasmid DNA/protamine/fish sperm DNA/stearic acid grafted chitosan oligosaccharide micelles for gene delivery

机译:由质粒DNA /鱼精蛋白/鱼精DNA /硬脂酸接枝的壳聚糖寡糖胶束组成的四元复合物,用于基因传递

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摘要

Quaternary complexes with condensed core of plasmid DNA, protamine, fish sperm DNA and shell of stearic acid grafted chitosan oligosaccharide (CSO-SA), were prepared. The CSO-SA could self-assemble to form nano-sized micelles in aqueous solution and demonstrated excellent internalization ability of tumor cells. Dynamic light scattering (DLS) measurement and transmission electrostatic microscope (TEM) images showed that quaternary complexes had spherical shape with about 25 nm number average diameter, and the size of quaternary complexes was smaller than that of CSO-SA micelles and CSO-SA micelles/plasmid DNA binary complexes. The transfection efficiencies of quaternary complexes on HEK293 and MCF-7 cells increased with incubation time, and were significantly higher than that of CSO-SA micelles/plasmid DNA binary complexes. The optimal transfection efficiency of quaternary complexes on HEK293 and MCF-7 cells measured by flow cytometer after 96 h was 23.82% and 41.43%, respectively. Whereas, the transfection efficiency of Lipofectamine? 2000 on HEK293 and MCF-7 cells after 96 h was 32.45% and 33.23%, respectively. The data of luciferease activity measurement showed that the optimal ratio of plasmid DNA:fish sperm DNA:protamine:CSO-SA was 1:1:5:5. The results indicated that the present quaternary complexes were potential non-viral gene delivery system.
机译:制备了带有质粒DNA,鱼精蛋白,鱼精DNA和硬脂酸接枝的壳聚糖寡糖(CSO-SA)壳的缩合核心的季盐复合物。 CSO-SA可以在水溶液中自组装形成纳米胶束,并具有优异的肿瘤细胞内在化能力。动态光散射(DLS)测量和透射电镜(TEM)图像显示,四元络合物呈球形,数均直径约为25 nm,且四元络合物的尺寸小于CSO-SA胶束和CSO-SA胶束/质粒DNA二元复合物。四元复合物在HEK293和MCF-7细胞上的转染效率随孵育时间的增加而增加,并且显着高于CSO-SA胶束/质粒DNA二元复合物。流式细胞仪检测HEK293和MCF-7细胞在96小时后的最佳转染效率分别为23.82%和41.43%。而Lipofectamine的转染效率如何?在96小时后,2000年HEK293和MCF-7细胞上的分别为32.45%和33.23%。荧光素酶活性测量数据表明,质粒DNA:鱼精DNA:鱼精蛋白:CSO-SA的最佳比例为1:1:5:5。结果表明,目前的四元复合物是潜在的非病毒基因传递系统。

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