Yu Changjiang, Zhao Jianjun, Guo Yingzhi, Lu Cailing, Ma Xu, Gu Zhongwei
Peking Union Medical College, Beijing 100730, People's Republic of China.
J Biomed Mater Res A. 2008 Nov;87(2):364-72. doi: 10.1002/jbm.a.31786.
A novel and simple method to form water-dispersed magnetic nanoparticles was successfully developed through glucosaminic acid-surface modification of iron oxide nanoparticles. The resultant glucosaminic acid-modified magnetic nanoparticles (GA-MNPs) had not only good uniformity in spherical shape with diameter of about 10-13 nm, but also possessed excellent water-dispersity and stability. In cell culture experiments, the internalization of GA-MNPs into different kinds of cells was observed over a 5-day period. The results indicated that the internalization of GA-MNPs into mouse macrophage cells and mouse embryonic fibroblast cells was not observed after 40 h of culturing. However, the GA-MNPs were internalized quickly into cancer cells after just 24 h of culturing. TEM images of the GA-MNPs uptake in ECA-109 cells were used to study the internalization mechanisms of GA-MNPs and their distribution in ECA-109 cells. Additionally, a water-dispersed magnetic capture probe was prepared by immobilization of oligonucleotides onto GA-MNPs, and the probe was used for detection and separation of their complementary oligonucleotides sequence.
通过对氧化铁纳米颗粒进行氨基葡萄糖表面修饰,成功开发出一种新颖且简单的制备水分散磁性纳米颗粒的方法。所得的氨基葡萄糖修饰磁性纳米颗粒(GA-MNPs)不仅具有良好的球形均匀性,直径约为10-13nm,还具有优异的水分散性和稳定性。在细胞培养实验中,在5天的时间内观察到GA-MNPs进入不同类型细胞的内化情况。结果表明,培养40小时后未观察到GA-MNPs进入小鼠巨噬细胞和小鼠胚胎成纤维细胞。然而,培养仅24小时后,GA-MNPs就迅速进入癌细胞。利用GA-MNPs在ECA-109细胞中摄取的透射电子显微镜(TEM)图像来研究GA-MNPs的内化机制及其在ECA-109细胞中的分布。此外,通过将寡核苷酸固定在GA-MNPs上制备了一种水分散磁性捕获探针,该探针用于检测和分离其互补寡核苷酸序列。
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