Gómez-Serranillos Isabel Rey, Miñones José, Dynarowicz-Łatka Patrycja, Iribarnegaray Eduardo, Casas Matilde
Department of Physical Chemistry, Faculty of Pharmacy, University of Santiago de Compostela, Spain.
Colloids Surf B Biointerfaces. 2005 Mar 10;41(1):63-72. doi: 10.1016/j.colsurfb.2004.11.004.
The ganglioside, GM1, was studied as Langmuir monolayers at the air/water interface with surface pressure-area measurements in addition to Brewster angle microscopy. A characteristic plateau transition, observed on aqueous subphases of pH 2 and 6, 20 degrees C, at the surface pressure of ca. 20 mN/m, was attributed to the reorientation of GM1 polar group upon film compression. This transition was found to disappear at alkaline subphases (pH 10) due to the hydration of fully ionized polar group, hindering its reorientation. The interactions between GM1 and hexadecylphosphocholine (miltefosine) were investigated in mixed monolayers and analyzed with the mean molecular areas, excess areas of mixing and the excess free energy of mixing versus film composition plots. The monolayers stability, quantified by the collapse pressure values, as well as the strength of interaction was found to diminish in the following order: pH 6>pH 2>pH 10. The strongest interaction occurs for mixed films of miltefosine molar fraction, XM=0.7-0.8, especially at low pressure region, and are explained as being due to the surface complex formation of 3:1 or 4:1 (miltefosine:ganglioside) stoichiometry (XM=0.75 or 0.8, respectively).
神经节苷脂GM1在空气/水界面被作为朗缪尔单分子层进行研究,除了采用布鲁斯特角显微镜外,还进行了表面压力-面积测量。在20℃、pH值为2和6的水相亚相中,在约20 mN/m的表面压力下观察到一个特征性的平台转变,这归因于GM1极性基团在膜压缩时的重新取向。由于完全电离的极性基团发生水合作用,阻碍了其重新取向,发现在碱性亚相(pH 10)中这种转变消失。在混合单分子层中研究了GM1与十六烷基磷酸胆碱(米替福新)之间的相互作用,并通过平均分子面积、混合超额面积以及混合超额自由能与膜组成关系图进行分析。通过崩溃压力值量化的单分子层稳定性以及相互作用强度按以下顺序减弱:pH 6>pH 2>pH 10。对于米替福新摩尔分数XM = 0.7 - 0.8的混合膜,尤其是在低压区域,会发生最强的相互作用,这被解释为是由于形成了化学计量比为3:1或4:1(米替福新:神经节苷脂)的表面复合物(分别对应XM = 0.75或0.8)。