Department of Pharmaceutical Technology, University of Regensburg, Universitaetsstrasse 31, 93053 Regensburg, Germany.
Small. 2012 Dec 21;8(24):3847-56. doi: 10.1002/smll.201201112. Epub 2012 Aug 22.
Because nanoparticles are finding uses in myriad biomedical applications, including the delivery of nucleic acids, a detailed knowledge of their interaction with the biological system is of utmost importance. Here the size-dependent uptake of gold nanoparticles (AuNPs) (20, 30, 50 and 80 nm), coated with a layer-by-layer approach with nucleic acid and poly(ethylene imine) (PEI), into a variety of mammalian cell lines is studied. In contrast to other studies, the optimal particle diameter for cellular uptake is determined but also the number of therapeutic cargo molecules per cell. It is found that 20 nm AuNPs, with diameters of about 32 nm after the coating process and about 88 nm including the protein corona after incubation in cell culture medium, yield the highest number of nanoparticles and therapeutic DNA molecules per cell. Interestingly, PEI, which is known for its toxicity, can be applied at significantly higher concentrations than its IC(50) value, most likely because it is tightly bound to the AuNP surface and/or covered by a protein corona. These results are important for the future design of nanomaterials for the delivery of nucleic acids in two ways. They demonstrate that changes in the nanoparticle size can lead to significant differences in the number of therapeutic molecules delivered per cell, and they reveal that the toxicity of polyelectrolytes can be modulated by an appropriate binding to the nanoparticle surface.
由于纳米颗粒在包括核酸传递在内的众多生物医学应用中得到了应用,因此详细了解它们与生物系统的相互作用至关重要。在这里,研究了通过逐层方法用核酸和聚(亚乙基亚胺)(PEI)涂覆的金纳米颗粒(AuNP)(20、30、50 和 80nm)的尺寸依赖性摄取进入各种哺乳动物细胞系。与其他研究不同,确定了细胞摄取的最佳粒径,还确定了每个细胞的治疗有效载荷分子的数量。结果发现,直径约为 32nm 的涂覆后直径为 20nm 的 AuNP 和包括孵育在细胞培养基中后的蛋白质冠在内的直径为 88nm 的 AuNP,每个细胞的纳米颗粒和治疗性 DNA 分子的数量最高。有趣的是,尽管众所周知 PEI 具有毒性,但可以在远高于其 IC(50)值的浓度下应用,这很可能是因为它紧密结合到 AuNP 表面上和/或被蛋白质冠覆盖。这些结果对于未来设计用于核酸传递的纳米材料有两种方式很重要。它们表明,纳米颗粒尺寸的变化会导致每个细胞中传递的治疗分子数量的显着差异,并且它们揭示了聚电解质的毒性可以通过与纳米颗粒表面的适当结合来调节。