Miñones J, Rey Gómez-Serranillos I, Conde O, Dynarowicz-Łatka P, Miñones Trillo J
Department of Physical Chemistry, Faculty of Pharmacy, Campus Sur, 15706 Santiago de Compostela, Spain.
J Colloid Interface Sci. 2006 Sep 1;301(1):258-66. doi: 10.1016/j.jcis.2006.04.059. Epub 2006 Jun 23.
Effects of the subphase temperature on the surface pressure (pi)-area (A) isotherms of mixed monolayers of miltefosine (hexadecylphosphocholine), a potential anticancer drug, and cholesterol were investigated at the air/water interface, which were supplemented with Brewster angle microscopy (BAM) observations. Comparison of the collapse pressure values, mean molecular areas, excess areas and excess free energy of mixing between the mixed monolayer at various molar ratios and the pure component monolayers showed that, regardless of the subphase temperature, the investigated miltefosine-cholesterol system is much more stable than that the pure component monolayers, suggesting strong attractive interactions between miltefosine and cholesterol in mixed monolayers. As a consequence, it was postulated that stable "complexes" of the two components could form at the interface, for which stoichiometry may vary with the subphase temperature. Such "surface complexes" should be responsible for the contraction of the mean molecular area and thus the high stability of the mixed monolayer.
在空气/水界面研究了亚相温度对潜在抗癌药物米替福新(十六烷基磷胆碱)与胆固醇混合单分子层的表面压力(π)-面积(A)等温线的影响,并辅以布儒斯特角显微镜(BAM)观察。比较不同摩尔比混合单分子层与纯组分单分子层之间的崩溃压力值、平均分子面积、过量面积和混合过量自由能,结果表明,无论亚相温度如何,所研究的米替福新-胆固醇体系比纯组分单分子层稳定得多,这表明混合单分子层中米替福新与胆固醇之间存在强烈的吸引相互作用。因此,推测两种组分在界面处可形成稳定的“复合物”,其化学计量可能随亚相温度而变化。这种“表面复合物”应是平均分子面积收缩以及混合单分子层具有高稳定性的原因。