López O, de la Maza A, Coderch L, López-Iglesias C, Wehrli E, Parra J L
Departamento de Tensioactivos, Centro de Investigación y Desarrollo, Consejo Superior de Investigaciones Científicas, Barcelona, Spain.
FEBS Lett. 1998 Apr 24;426(3):314-8. doi: 10.1016/s0014-5793(98)00363-9.
The vesicle to micelle transition which results in the interaction of the Triton X-100 surfactant with phosphatidylcholine vesicles was studied by means of dynamic light scattering (at different reading angles) and by freeze-fracture electron microscopy techniques. Vesicle solubilization was produced by the direct formation of mixed micelles without the formation of complex intermediate aggregates. Thus, vesicle to micelle transformation was mainly governed by the progressive formation of mixed micelles within the bilayer. A subsequent separation of these micelles from the liposome surface (vesicle perforation by the formation of surfactant-stabilized holes on the vesicle surface) led to a complete solubilization of liposomes.
通过动态光散射(在不同读取角度)和冷冻断裂电子显微镜技术,研究了导致Triton X - 100表面活性剂与磷脂酰胆碱囊泡相互作用的囊泡到胶束的转变。囊泡的溶解是通过直接形成混合胶束而产生的,没有形成复杂的中间聚集体。因此,囊泡到胶束的转变主要由双层内混合胶束的逐步形成所控制。随后这些胶束从脂质体表面分离(通过在囊泡表面形成表面活性剂稳定的孔使囊泡穿孔)导致脂质体完全溶解。