Kabanov V A, Yaroslavov A A
Polymer Department, School of Chemistry, M.V. Lomonosov Moscow State University, Leninskie Gory, 119899, Moscow, Russia.
J Control Release. 2002 Jan 17;78(1-3):267-71. doi: 10.1016/s0168-3659(01)00496-5.
Complexation of synthetic polycations with negative lipid vesicles as cell-mimetic species was studied. It was found that such interaction could be accompanied by lateral lipid segregation, highly accelerated transmembrane migration of lipid molecules (polycation-induced flip-flop), incorporation of adsorbed polycations into vesicular membrane as well as aggregation and disruption of vesicles. A polycation adsorbed on the surface of liquid vesicles due to electrostatic attraction could be completely removed from the membrane by increase in simple salt concentration or by recomplexation with polyanions. In contrast, adsorption of a polycation carrying pendant hydrophobic groups was irreversible apparently due to incorporation of these groups into the hydrophobic part of the vesicular membrane. The above mentioned phenomena were examined depending on the polycation structure, fraction of charged lipids in the membrane, vesicle phase state and ionic strength of solution.
研究了合成聚阳离子与作为细胞模拟物的负电荷脂质囊泡的络合作用。发现这种相互作用可能伴随着脂质侧向分离、脂质分子的跨膜迁移高度加速(聚阳离子诱导的翻转)、吸附的聚阳离子掺入囊泡膜以及囊泡的聚集和破裂。由于静电吸引吸附在液体囊泡表面的聚阳离子可以通过增加简单盐浓度或与聚阴离子再络合而从膜上完全去除。相比之下,携带侧链疏水基团的聚阳离子的吸附显然是不可逆的,这是由于这些基团掺入了囊泡膜的疏水部分。根据聚阳离子结构、膜中带电脂质的比例、囊泡相态和溶液的离子强度对上述现象进行了研究。