Wurster Eva-Christina, Elbakry Asmaa, Göpferich Achim, Breunig Miriam
Department of Pharmaceutical Technology, University of Regensburg, Regensburg, Germany.
Methods Mol Biol. 2013;948:171-82. doi: 10.1007/978-1-62703-140-0_12.
The delivery of nucleic acids to mammalian cells requires a potent particulate carrier system. The physicochemical properties of the used particles, such as size and surface charge, strongly influence the cellular uptake and thereby the extent of the subsequent biological effect. However the knowledge of this process is still fragmentary because heterogeneous particle collectives are applied. Therefore we present a strategy to synthesize carriers with a highly specific appearance on the basis of gold nanoparticles (AuNPs) and the Layer-by-Layer (LbL) technique. The LbL method is based on the alternate deposition of oppositely charged (bio-)polymers, in our case poly(ethylenimine) and nucleic acids. The size and surface charge of those particles can be easily modified and accordingly systematic studies on cellular uptake are accessible.
将核酸递送至哺乳动物细胞需要一种高效的颗粒载体系统。所用颗粒的物理化学性质,如大小和表面电荷,会强烈影响细胞摄取,进而影响后续生物学效应的程度。然而,由于应用的是异质颗粒聚集体,对这一过程的了解仍然支离破碎。因此,我们提出了一种基于金纳米颗粒(AuNPs)和层层(LbL)技术合成具有高度特异性外观的载体的策略。LbL方法基于带相反电荷的(生物)聚合物的交替沉积,在我们的案例中是聚乙烯亚胺和核酸。这些颗粒的大小和表面电荷可以很容易地改变,因此可以进行关于细胞摄取的系统研究。