Zhang Enqi, Fu Ailing
School of Pharmaceutical Sciences, Southwest University, Chongqing, People's Republic of China.
Int J Nanomedicine. 2015 Mar 16;10:2115-24. doi: 10.2147/IJN.S78554. eCollection 2015.
Despite the significant progress in molecular imaging technologies that has been made in recent years, the specific detection of neural cells still remains challenging. Here, we suggest the use of gold nanoclusters (AuNCs) modified with a brain-targeting peptide as a potential imaging candidate for detecting neural cells in vitro and in mice. AuNCs of less than 10 nm (dynamic light scattering analysis) were first prepared using the "green" synthetic approach, and then a targeting peptide, rabies virus glycoprotein derived peptide (RDP), was conjugated to the AuNCs for improving the efficiency and specificity of neural cell penetration. The conjugate's mechanism of cellular attachment and entry into neural cells was suggested to be receptor-mediated endocytosis through clathrin-coated pits. Also, noninvasive imaging analysis and animal studies indicated that the RDP-modified nanoclusters could concentrate in the brain and locate in neural cells. This study suggests the feasibility of using targeting peptide-modified nanoclusters for noninvasive imaging brain cells in vivo.
尽管近年来分子成像技术取得了显著进展,但神经细胞的特异性检测仍然具有挑战性。在此,我们建议使用经脑靶向肽修饰的金纳米团簇(AuNCs)作为在体外和小鼠体内检测神经细胞的潜在成像候选物。首先使用“绿色”合成方法制备小于10 nm的AuNCs(动态光散射分析),然后将靶向肽狂犬病病毒糖蛋白衍生肽(RDP)与AuNCs偶联,以提高神经细胞穿透的效率和特异性。推测该偶联物与神经细胞的附着和进入机制是通过网格蛋白包被小窝的受体介导的内吞作用。此外,非侵入性成像分析和动物研究表明,RDP修饰的纳米团簇可以在脑中聚集并定位在神经细胞中。这项研究表明了使用靶向肽修饰的纳米团簇在体内对脑细胞进行非侵入性成像的可行性。