Hac-Wydro Katarzyna, Dynarowicz-Łatka Patrycja
Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Kraków, Poland.
Colloids Surf B Biointerfaces. 2006 Nov 1;53(1):64-71. doi: 10.1016/j.colsurfb.2006.07.015. Epub 2006 Aug 2.
The paper presents a thorough characteristics of Langmuir monolayers formed at the air/water interface by a polyene macrolide antibiotic-nystatin. The investigations are based on the analysis of pi/A isotherms recorded for monolayers formed by this antibiotic at different experimental conditions. A significant part of this work is devoted to the stability and relaxation phenomena. It has been found that nystatin forms at the air/water interface monolayers of the LE state. A plateau region, observed during the course of the isotherm compression, is suggested to be due to the orientational change of nystatin molecules from horizontal to vertical position. Quantitative analysis of the desorption of the monolayer material into bulk water indicates that the solubility of nystatin monolayers increases with surface pressure. At low surface pressures, the desorption of nystatin from a monolayer is controlled both by dissolution and by diffusion. However, at the plateau and in the post-plateau region, the desorption does not achieve a steady state and the monolayer is less stable than in the pre-plateau region. However, the presence of membrane lipids, even at a low mole fraction, considerably increases the stability of nystatin monolayers. This enables the application of the Langmuir monolayer technique to study nystatin in mixture with cellular membrane components, aiming at verifying its mode of action and the mechanism of toxicity.
本文全面介绍了多烯大环内酯类抗生素制霉菌素在空气/水界面形成的朗缪尔单分子层的特性。研究基于对该抗生素在不同实验条件下形成的单分子层所记录的π/A等温线的分析。这项工作的很大一部分致力于稳定性和弛豫现象。已发现制霉菌素在空气/水界面形成LE态的单分子层。等温线压缩过程中观察到的一个平台区域被认为是由于制霉菌素分子从水平位置到垂直位置的取向变化所致。对单分子层物质解吸到本体水中的定量分析表明,制霉菌素单分子层的溶解度随表面压力增加。在低表面压力下,制霉菌素从单分子层的解吸受溶解和扩散共同控制。然而,在平台区和平台后区域,解吸未达到稳态,且单分子层比平台前区域更不稳定。然而,即使在低摩尔分数下,膜脂的存在也会显著增加制霉菌素单分子层的稳定性。这使得朗缪尔单分子层技术能够用于研究制霉菌素与细胞膜成分的混合物,旨在验证其作用方式和毒性机制。