Yaghmur Anan, de Campo Liliana, Sagalowicz Laurent, Leser Martin E, Glatter Otto
Institute of Chemistry, University of Graz, A-8010 Graz, Austria, and Nestlé Research Center, Lausanne, Switzerland.
Langmuir. 2006 Nov 21;22(24):9919-27. doi: 10.1021/la061303v.
This work describes the effect of two different surfactants on the internal nanostructure of the kinetically stabilized isasomes (internally self-assembled particles or "somes"), which are a new family of colloidal particles (cubosomes, hexosomes, micellar cubosomes, and emulsified microemulsions, EME). The stabilization of these systems is performed by using the polymeric stabilizer F127. We demonstrate that the internal structure of these oil-free and oil-loaded dispersed particles can be modulated by varying the lipid composition. To achieve this goal, we replaced part of our primary lipid monolinolein (MLO) with diglycerol monooleate (DGMO) or soybean phosphatidylcholine (PC). We found that DGMO has a counter effect to that of tetradecane (TC) and allows us to tune back the self-assembled nanostructure in the TC-loaded dispersions from H2 (hexosomes) to Im3m (cubosomes). Although TC has a higher impact on confined structures than does DGMO, we demonstrate that the addition of DGMO significantly affects the internal structure of the TC-solubilized dispersions and favors the formation of large water channels. PC can also be used to modify the internal structure for MLO-based systems. It is somehow different from DGMO due to the fact that the fully hydrated Pn3m cubic structure in the presence of PC for the TC-free dispersion is preserved after dispersing. The results also indicate that PC is less effective than DGMO for tuning back the TC-loaded internal structure from H2 to cubic phase, in which it makes the confined structure less ordered. In addition, we found that DGMO has a significant effect on the internal structure of isasomes. It increases the water solubilization capacity for dispersed and nondispersed bulk phases. In contrast to the MLO-based dispersions, the present results indicate that F127 plays an important role in the internal structure of these dispersions due to its penetration into the oil-free cubic phase changing the symmetry from Pn3m to Im3m.
本研究描述了两种不同表面活性剂对动力学稳定的异质体(内部自组装颗粒或“体”)内部纳米结构的影响,异质体是一类新型胶体颗粒(立方相液晶、六方相液晶、胶束立方相液晶和乳化微乳液,即EME)。这些体系通过使用聚合物稳定剂F127来实现稳定。我们证明,通过改变脂质组成,可以调节这些无油和载油分散颗粒的内部结构。为实现这一目标,我们用甘油单油酸酯(DGMO)或大豆磷脂酰胆碱(PC)替代了部分主要脂质单油酸甘油酯(MLO)。我们发现,DGMO对十四烷(TC)具有相反的作用,使我们能够将载TC分散体中的自组装纳米结构从H2(六方相液晶)调回Im3m(立方相液晶)。尽管TC对受限结构的影响比DGMO更大,但我们证明,添加DGMO会显著影响TC增溶分散体的内部结构,并有利于形成大的水通道。PC也可用于修饰基于MLO的体系的内部结构。它与DGMO有所不同,因为在无TC分散体中存在PC时,完全水合的Pn3m立方结构在分散后得以保留。结果还表明,在将载TC的内部结构从H2调回立方相方面,PC的效果不如DGMO,这使得受限结构的有序性降低。此外,我们发现DGMO对异质体的内部结构有显著影响。它增加了分散相和非分散体相的水增溶能力。与基于MLO的分散体不同,目前的结果表明,F127由于渗透到无油立方相中,使对称性从Pn3m变为Im3m,从而在这些分散体的内部结构中发挥重要作用。