Institute of Pharmaceutical Technology, Goethe-University, Frankfurt am Main, Germany.
J Microencapsul. 2013;30(1):49-54. doi: 10.3109/02652048.2012.692491. Epub 2012 Jun 7.
In 1995 it was reported for the first time that nanoparticles could be used for the delivery of drugs across the blood-brain barrier (BBB) following intravenous injection. In vitro and in vivo experiments show that the underlying mechanism is receptor-mediated endocytosis followed by transcytosis. No opening of the tight junctions was observed. Due to the overcoating of the nanoparticles with polysorbate 80 or poloxamers 188, apolipoproteins A-I and/or E are adsorbed from the blood on to the particle surface after injection. These apolipoproteins mediate the interaction with LDL or scavenger receptors on the BBB followed by the above brain uptake processes. Likewise, covalent attachment of these apolipoproteins or of transferrin, insulin or antibodies against the respective receptors also enables a similar nanoparticle-mediated drug transport across the BBB. From these results it can be concluded that the nanoparticles act as "Trojan Horses" taking advantage of physiological receptor-mediated transport processes across the BBB.
1995 年首次报道,纳米颗粒可以通过静脉注射用于穿过血脑屏障(BBB)递药。体外和体内实验表明,其潜在机制是受体介导的内吞作用,随后是跨细胞转运。观察到没有紧密连接的打开。由于纳米颗粒用聚山梨酯 80 或泊洛沙姆 188 过度包被,在注射后,载脂蛋白 A-I 和/或 E 从血液中吸附到颗粒表面。这些载脂蛋白介导与 LDL 或清道夫受体的相互作用,随后是上述脑摄取过程。同样,这些载脂蛋白或转铁蛋白、胰岛素或针对相应受体的抗体的共价连接也能够使类似的纳米颗粒介导的药物穿过 BBB 转运。从这些结果可以得出结论,纳米颗粒充当“特洛伊木马”,利用生理受体介导的穿过 BBB 的转运过程。