Pantos Alexandros, Sideratou Zili, Paleos Constantinos M
Institute of Physical Chemistry, NCSR Demokritos, 15310 Aghia Paraskevi, Attiki, Greece.
J Colloid Interface Sci. 2002 Sep 15;253(2):435-42. doi: 10.1006/jcis.2002.8567.
A prospective targeted drug delivery system was prepared by the introduction of complementary and protective moieties at the external surfaces of liposomes. Thus recognition between hydrogenated phosphatidylcholine-cholesterol-based liposomes was achieved by the interaction of the complementary phosphate and guanidinium groups incorporated in separate liposomes while polyethylene glycol chains (PEG) protected both liposomes from environmental factors. In general, protective coating of liposomes in the range of 5% molar incorporation exerted an inhibitory effect on their recognition but it also permitted effective interaction between complementary liposomes.
通过在脂质体的外表面引入互补和保护部分,制备了一种前瞻性靶向给药系统。因此,基于氢化磷脂酰胆碱-胆固醇的脂质体之间的识别是通过掺入不同脂质体中的互补磷酸基团和胍基团之间的相互作用实现的,而聚乙二醇链(PEG)保护两种脂质体免受环境因素影响。一般来说,摩尔掺入量在5%范围内的脂质体保护涂层对它们的识别有抑制作用,但也允许互补脂质体之间进行有效相互作用。