Nikolova A N, Jones M N
Institute of Physical Chemistry, Bulgarian Academy of Sciences, Sofia 1113, Bulgaria.
Biochim Biophys Acta. 1998 Jul 17;1372(2):237-43. doi: 10.1016/s0005-2736(98)00061-3.
Free thin liquid films (foam films) formed from aqueous dispersions of dimyristoylphosphatidylcholine (DMPC) and dipalmitoylphosphatidylethanolamine with covalently bound poly-(ethylene glycol) of molecular weight 2000 (DPPE-PEG-2000) were studied by the thin liquid film microinterferometric technique of Scheludko and Exerowa in the temperature range 14-36 degrees C. The surface tension kinetics of the dispersions were studied in order to ensure equilibration of the foam films. These measurements showed that the rate of surface coverage depends slightly on the temperature and does not reach equilibrium values within reasonable time intervals for the dispersions containing only one amphiphile (DPPE-PEG-2000). The destruction of the vesicles at the air/(aqueous dispersion) interface was much faster for the dispersions containing DMPC/DPPE-PEG-2000 mixtures above 23 degrees C, the temperature of the chain-melting phase transition of the main lipid component (DMPC). The dependence of the equilibrium thickness of the foam films on the electrolyte concentration was measured for 1 and 9 mol% DPPE-PEG-2000 at 28 degrees C in the range 10-3 to 0.5 M NaCl. These results indicate that at the low electrolyte concentrations the electrostatic and van der Waals interactions are dominant similar to the foam films stabilized with DMPC alone. At the high electrolyte concentrations the steric repulsion of the PEG layers becomes dominant. The temperature-composition dependence of the bilayer thickness was measured for the foam bilayers at 0.14 M NaCl. The data for the foam bilayer thickness and the comparison with the phase diagrams of PC/PE-PEG dispersions, show that the DMPC/DPPE-PEG-2000 foam bilayers are able to exist in two phase states characterised by different conformations (mushroom and brush) of the grafted polymer.
采用舍卢德科和埃克塞罗娃的薄液膜微干涉技术,在14至36摄氏度的温度范围内,研究了由二肉豆蔻酰磷脂酰胆碱(DMPC)和与分子量为2000的共价结合聚乙二醇(DPPE - PEG - 2000)的二棕榈酰磷脂酰乙醇胺的水分散体制备的自由薄液膜(泡沫膜)。为确保泡沫膜达到平衡,研究了分散体的表面张力动力学。这些测量表明,表面覆盖速率对温度的依赖性较小,对于仅含一种两亲物(DPPE - PEG - 2000)的分散体,在合理的时间间隔内未达到平衡值。对于含有DMPC/DPPE - PEG - 2000混合物且温度高于23摄氏度(主要脂质成分(DMPC)的链熔化相变温度)的分散体,空气/(水分散体)界面处囊泡的破坏要快得多。在28摄氏度下,测量了1 mol%和9 mol% DPPE - PEG - 2000时泡沫膜平衡厚度对电解质浓度在10⁻³至0.5 M NaCl范围内的依赖性。这些结果表明,在低电解质浓度下,静电相互作用和范德华相互作用起主导作用,类似于仅用DMPC稳定的泡沫膜。在高电解质浓度下,PEG层的空间排斥作用起主导作用。在0.14 M NaCl下测量了泡沫双层膜双层厚度的温度 - 组成依赖性。泡沫双层膜厚度的数据以及与PC/PE - PEG分散体相图的比较表明,DMPC/DPPE - PEG - 2000泡沫双层膜能够以两种相态存在,其特征是接枝聚合物具有不同的构象(蘑菇状和刷状)。