Universität Hamburg, Institute for Physical Chemistry, Grindelallee 117, 20146 Hamburg, Germany.
Nanoscale. 2017 Oct 5;9(38):14486-14498. doi: 10.1039/c7nr02973j.
The delivery of gold nanoparticles (AuNPs) to specific cells strongly depends on the properties e.g. the size of the particles and is of great interest for a large variety of biomedical applications. Here we investigated the size dependence of the receptor-ligand mediated AuNP delivery to cells by comparing very small "molecular" Au-clusters of only 2 nm to larger 7 nm and 36 nm AuNPs with a distinct surface plasmon resonance. Since the molecular weight in this range changes by almost three orders of magnitude, we show how the amount of gold relates to the number of delivered AuNPs. We attached small interleukin-6 receptor (IL-6R) specific aptamer molecules (AIR-3A) in different amounts to the particles and investigated the specificity of the delivery to IL-6R-carrying cells. To reduce unspecific interaction the particles were additionally covered with polyethylene glycol (PEG). Besides particle size and concentration we varied additional parameters such as aptamer surface coverage as well as incubation time and temperature. We found that in particular, small particles with diameters of less than 2 nm show an up to six times higher delivery rate for the aptamer-conjugated AuNPs compared to untargeted PEG-coated AuNPs. The specificity reduces with a decreasing aptamer/PEG ratio, and also with an increase in particle size where the unspecific uptake is much higher. In addition we also compared the delivery efficiency of this aptamer-mediated delivery system with an antibody-mediated system targeting the same receptor to validate the performance of this approach.
金纳米粒子(AuNPs)递送到特定细胞强烈依赖于例如粒子的大小等性质,这对于各种生物医学应用都具有重要意义。在这里,我们通过比较具有明显表面等离子体共振的仅 2nm 的非常小的“分子”Au 簇与 7nm 和 36nm 的 AuNPs,研究了受体配体介导的 AuNP 向细胞输送的尺寸依赖性。由于在此范围内分子量变化了近三个数量级,因此我们展示了金的数量与输送的 AuNPs 数量之间的关系。我们将不同数量的小白细胞介素 6 受体(IL-6R)特异性适体分子(AIR-3A)附着到颗粒上,并研究了将其递送到携带 IL-6R 的细胞的特异性。为了减少非特异性相互作用,颗粒还额外用聚乙二醇(PEG)覆盖。除了颗粒大小和浓度外,我们还改变了其他参数,如适体表面覆盖率以及孵育时间和温度。我们发现,特别是直径小于 2nm 的小颗粒,与未靶向的 PEG 包覆的 AuNPs 相比,靶向 IL-6R 的缀合 AuNPs 的输送率要高 6 倍。特异性随着适体/PEG 比的降低而降低,随着颗粒尺寸的增加而降低,其中非特异性摄取要高得多。此外,我们还将这种适体介导的递药系统与靶向相同受体的抗体介导系统的递药效率进行了比较,以验证这种方法的性能。