Dörfler H D
Sektion Chemie, TU Dresden, G.D.R.
Adv Colloid Interface Sci. 1990 Feb;31(1-2):1-110. doi: 10.1016/0001-8686(90)80003-i.
The detailed miscibility analysis of binary phospholipid monolayers requires the application of a variety of spreading and surface techniques which often yield complementary results. Testing the equilibrium state of the binary monolayer by long-time experiments is also of great importance. Studies of the compression and spreading behavior of binary monomolecular systems form a basis for the determination of binary monomolecular phase diagrams. Within these plots different phase regions occur which permit clear statements regarding the miscibility state. Additional knowledge of the miscibility properties (phase diagrams) of the binary bulk systems is required. From the analogy of the properties of the bulk systems, the miscibility state of the monolayers is also determined by the temperature, and we can classify the monolayers of binary lecithin and cephalin systems into systems of complete miscibility, partial miscibility and complete immiscibility. In addition to the differences in the chemical structure of the mixing components, the film states in the monolayer and the miscibility behavior of the bulk systems are also influencing factors. If one of the components does not produce a spreading pressure, miscibility gaps occur in the phase diagram of the phospholipid monolayer. The miscibility gap, expressed by a constant spreading pressure, indicates complete immiscibility within this concentration range. If both components produce spreading pressures, and condensed and liquid-expanded film states within the considered temperature range, partial miscibility of the components becomes probable. The most effective parameter is then the difference in the chemical structure of the components. When both components produce spreading pressures and condensed films, the chemical structure of the mixing phospholipid compounds within their hydrophilic and hydrophobic parts is of essential importance. Depending on the differences in the chemical structures of their chains and their head groups in the case of binary phospholipid monolayers, the following possibilities result: complete miscibility, partial miscibility and complete immiscibility of the lecithins and the cephalins. Complete miscibility within the binary phospholipid monolayer takes place in the case of identical head-group structure and where there are only small differences in the chain length of the fatty acid groups. With increasing hydrocarbon chain length differences, partial miscibility or even complete immiscibility can occur within the monolayer. Chemical differences in the head-group structure of the mixing components have a similar influence. In the case of binary lecithin/cephalin mixtures, the differences in the head-group structure affect the miscibility behavior more than the chain length differences do in the case of lecithin/lecithin and cephalin/cephalin mixtures.(ABSTRACT TRUNCATED AT 400 WORDS)
二元磷脂单分子层的详细混溶性分析需要应用多种铺展和表面技术,这些技术常常能产生互补的结果。通过长时间实验来测试二元单分子层的平衡状态也非常重要。二元单分子体系的压缩和铺展行为研究是确定二元单分子相图的基础。在这些相图中会出现不同的相区,据此可以对混溶状态做出清晰的判断。还需要了解二元本体体系的混溶性质(相图)的更多知识。根据本体体系性质的类推,单分子层的混溶状态也由温度决定,我们可以将二元卵磷脂和脑磷脂体系的单分子层分为完全混溶、部分混溶和完全不混溶体系。除了混合组分化学结构的差异外,单分子层中的膜状态和本体体系的混溶行为也是影响因素。如果其中一种组分不产生铺展压力,磷脂单分子层的相图中就会出现混溶间隙。由恒定铺展压力表示的混溶间隙表明在该浓度范围内完全不混溶。如果两种组分都产生铺展压力,并且在所考虑的温度范围内存在凝聚态和液体膨胀态膜,则组分可能部分混溶。此时最有效的参数是组分化学结构的差异。当两种组分都产生铺展压力和凝聚态膜时,混合磷脂化合物在其亲水和疏水部分的化学结构至关重要。对于二元磷脂单分子层,根据其链结构和头基结构的差异,会出现以下几种情况:卵磷脂和脑磷脂完全混溶、部分混溶和完全不混溶。当头部基团结构相同时,且脂肪酸基团的链长差异很小,二元磷脂单分子层内会发生完全混溶。随着烃链长度差异的增加,单分子层内可能出现部分混溶甚至完全不混溶。混合组分头部基团结构的化学差异也有类似影响。在二元卵磷脂/脑磷脂混合物中,头部基团结构的差异对混溶行为的影响比卵磷脂/卵磷脂和脑磷脂/脑磷脂混合物中链长差异的影响更大。(摘要截选至400字)