层状结构
膜
聚合物
自愈水凝胶
乙二醇
PEG比率
化学工程
化学
层状相
相(物质)
胶束
材料科学
高分子化学
色谱法
结晶学
有机化学
水溶液
生物化学
财务
工程类
经济
作者
Heidi E. Warriner,Stefan H. J. Idziak,Nelle L. Slack,Patrick Davidson,Cyrus R. Safinya
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1996-02-16
卷期号:271 (5251): 969-973
被引量:182
标识
DOI:10.1126/science.271.5251.969
摘要
A class of lamellar biological hydrogels comprised of fluid membranes of lipids and surfactants with small amounts of low molecular weight poly(ethylene glycol)-derived polymer lipids (PEG-lipids) were studied by x-ray diffraction, polarized light microscopy, and rheometry. In contrast to isotropic hydrogels of polymer networks, these membrane-based birefringent liquid crystalline biogels, labeled L α ,g , form the gel phase when water is added to the liquid-like lamellar L α phase, which reenters a liquid-like mixed phase upon further dilution. Furthermore, gels with larger water content require less PEG-lipid to remain stable. Although concentrated (∼50 weight percent) mixtures of free PEG (molecular weight, 5000) and water do not gel, gelation does occur in mixtures containing as little as 0.5 weight percent PEG-lipid. A defining signature of the L α ,g regime as it sets in from the fluid lamellar Lα phase is the proliferation of layer-dislocation-type defects, which are stabilized by the segregation of PEG-lipids to the defect regions of high membrane curvature that connect the membranes.
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