Department of Biomedical Engineering Washington University. St. Louis, MO 63130, USA.
Small. 2010 Feb 22;6(4):517-22. doi: 10.1002/smll.200901622.
In this study, we examined the effects of size, shape, and surface chemistry of gold nanostructures on their uptake (including both adsorption and internalization) by SK-BR-3 breast cancer cells. We used both spherical and cubic Au nanostructures (nanospheres and nanocages, respectively) of two different sizes, and their surface was modified with poly(ethylene glycol) (PEG), antibody anti-HER2, or poly(allyamine hydrochloride) (PAA). Our results showed that the size of the Au nanostructures influenced their uptake by the cells in a similar way regardless of the surface chemistry, while the shape dependency could vary depending on the surface functional group. In addition, the cells preferred to take up the Au nanostructures covered by different surface groups in the following order: PAA>> anti-HER2> PEG. The fraction of Au nanostructures attached to the cell surface was also dependent on the aforementioned parameters.
在这项研究中,我们研究了金纳米结构的大小、形状和表面化学性质对其被 SK-BR-3 乳腺癌细胞摄取(包括吸附和内化)的影响。我们使用了两种不同大小的球形和立方金纳米结构(纳米球和纳米笼),并对其表面进行了聚乙二醇(PEG)、抗 HER2 抗体或聚烯丙胺盐酸盐(PAA)的修饰。我们的结果表明,无论表面化学性质如何,金纳米结构的大小以相似的方式影响其被细胞摄取,而形状依赖性可能取决于表面官能团。此外,细胞更喜欢以下顺序摄取不同表面基团覆盖的金纳米结构:PAA>>抗 HER2>PEG。附着在细胞表面的金纳米结构的分数也取决于上述参数。