De la Maza A, Parra J L
Departamento de Tensioactivos, Centro de Investigación y Desarrollo (C.I.D.), Barcelona, Spain.
Biochem J. 1994 Nov 1;303 ( Pt 3)(Pt 3):907-14. doi: 10.1042/bj3030907.
The structural transition stages induced by the interaction of the non-ionic surfactant Triton X-100 on phosphatidylcholine unilamellar vesicles were studied by means of static and dynamic light-scattering, transmission-electron-microscopy (t.e.m.) and permeability changes. A linear correlation was observed between the effective surfactant/lipid molar ratios (Re) ('three-stage' model proposed for the vesicle solubilization) and the surfactant concentration throughout the process. However, this correlation was not noted for the partition coefficients of the surfactant between the bilayer and the aqueous medium (K). Thus a sharp initial K increase was observed until a maximum value was achieved for permeability alterations of 50% (initial step of bilayer saturation). Further surfactant additions resulted in a fall in the K values until 100% of bilayer permeability. Additional amounts of surfactant led to an increase in K until bilayer solubilization. Hence, a preferential incorporation of surfactant molecules into liposomes governs the initial interaction steps, leading to the initial stage of bilayer saturation with a free surfactant concentration that was lower than its critical micelle concentration (c.m.c.). Additional amounts of surfactant increased the free surfactant until the c.m.c. was reached, after which solubilization started to occur. Thus the initial step of bilayer saturation was achieved for a smaller surfactant concentration than that for the Resat, although this concentration was the minimum needed for solubilization to start. Large unilamellar vesicles began to form as the surfactant exceeded 15 mol% (50% bilayer permeability), the maximum vesicle growth being attained for 22 mol% (400 nm). Thereafter, static light-scattering started to decrease gradually, this fall being more pronounced after 40 mol%. The t.e.m. picture for 40 mol% (Resat.) showed unilamellar vesicles, although with traces of smaller structures. From 50 mol% the size distribution curves began to show a bimodal distribution. The t.e.m. pictures for 50-64 mol% revealed tubular structures, together with open bilayer fragments. Thereafter, increasing amounts of surfactant (65-69 mol%) led to planar multilayered structures which gradually tended to form concentric and helicoidal conformations. The scattered intensity decreased to a low constant value at more than 71-72 mol%. However, the surfactant concentration for the Re(sol) (72.6 mol %) still presented traces of aggregated structures, albeit with mono-modal size-distribution curves (particle size of 50 nm). This vesicle size corresponded to the liposome solubilization via mixed-micelle formation.
通过静态和动态光散射、透射电子显微镜(t.e.m.)以及渗透率变化研究了非离子表面活性剂吐温X-100与磷脂酰胆碱单层囊泡相互作用所诱导的结构转变阶段。在整个过程中,有效表面活性剂/脂质摩尔比(Re)(为囊泡增溶提出的“三阶段”模型)与表面活性剂浓度之间观察到线性相关性。然而,对于表面活性剂在双层与水相介质之间的分配系数(K),未观察到这种相关性。因此,观察到K值在初始阶段急剧增加,直到渗透率变化达到50%(双层饱和的初始步骤)时达到最大值。进一步添加表面活性剂导致K值下降,直到双层渗透率达到100%。额外添加表面活性剂会导致K值增加,直到双层增溶。因此,表面活性剂分子优先掺入脂质体决定了初始相互作用步骤,导致双层饱和的初始阶段,此时游离表面活性剂浓度低于其临界胶束浓度(c.m.c.)。额外添加表面活性剂会增加游离表面活性剂,直到达到c.m.c.,此后开始发生增溶。因此,双层饱和的初始步骤所需的表面活性剂浓度低于Resat所需的浓度,尽管该浓度是开始增溶所需的最低浓度。当表面活性剂超过15 mol%(双层渗透率50%)时,大单层囊泡开始形成,在22 mol%(400 nm)时达到最大囊泡生长。此后,静态光散射开始逐渐下降,在40 mol%之后这种下降更为明显。40 mol%(Resat.)的t.e.m.图像显示为单层囊泡,尽管有少量较小结构的痕迹。从50 mol%开始,尺寸分布曲线开始呈现双峰分布。50 - 64 mol%的t.e.m.图像显示出管状结构以及开放的双层片段。此后,增加表面活性剂用量(65 - 69 mol%)会导致形成平面多层结构,这些结构逐渐倾向于形成同心和螺旋构象。在超过71 - 72 mol%时,散射强度降至低恒定值。然而,Re(sol)(72.6 mol %)时的表面活性剂浓度仍呈现出聚集结构的痕迹,尽管尺寸分布曲线为单峰(粒径50 nm)。这种囊泡尺寸对应于通过混合胶束形成实现的脂质体增溶。