More than a monolayer: Relating lung surfactant structure and mechanics to composition

被引:136
作者
Alonso, C
Alig, T
Yoon, J
Bringezu, F
Warriner, H
Zasadzinski, JA [1 ]
机构
[1] Univ Calif Santa Barbara, Dept Chem Engn, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Mat, Santa Barbara, CA 93106 USA
[3] Univ Leipzig, Inst Med Phys & Biophys, D-04103 Leipzig, Germany
关键词
D O I
10.1529/biophysj.104.051201
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Survanta, a clinically used bovine lung surfactant extract, in contact with surfactant in the subphase, shows a coexistence of discrete monolayer islands of solid phase coexisting with continuous multilayer "reservoirs'' of fluid phase adjacent to the air-water interface. Exchange between the monolayer, the multilayer reservoir, and the subphase determines surfactant mechanical properties such as the monolayer collapse pressure and surface viscosity by regulating solid-fluid coexistence. Grazing incidence x-ray diffraction shows that the solid phase domains consist of two-dimensional crystals similar to those formed by mixtures of dipalmitoylphosphatidylcholine and palmitic acid. The condensed domains grow as the surface pressure is increased until they coalesce, trapping protrusions of liquid matrix. At similar to40 mN/m, a plateau exists in the isotherm at which the solid phase fraction increases from similar to60 to 90%, at which the surface viscosity diverges. The viscosity is driven by the percolation of the solid phase domains, which depends on the solid phase area fraction of the monolayer. The high viscosity may lead to high monolayer collapse pressures, help prevent atelectasis, and minimize the flow of lung surfactant out of the alveoli due to surface tension gradients.
引用
收藏
页码:4188 / 4202
页数:15
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