Warriner H E, Idziak S H, Slack N L, Davidson P, Safinya C R
Materials Research Laboratory, Materials Department, University of California, Santa Barbara 93106, USA.
Science. 1996 Feb 16;271(5251):969-73. doi: 10.1126/science.271.5251.969.
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-alpha,g, form the gel phase when water is added to the liquid-like lamellar L-alpha 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 (approximately 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-alpha,g regime as it sets in from the fluid lamellar L-alpha 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.
通过X射线衍射、偏光显微镜和流变学对一类由脂质和表面活性剂的流体膜以及少量低分子量聚乙二醇衍生的聚合物脂质(PEG-脂质)组成的层状生物水凝胶进行了研究。与聚合物网络的各向同性水凝胶不同,这些基于膜的双折射液晶生物凝胶(标记为L-α,g),当向类液体层状L-α相中加入水时形成凝胶相,进一步稀释时又重新进入类液体混合相。此外,含水量较大的凝胶需要较少的PEG-脂质来保持稳定。虽然游离PEG(分子量5000)和水的浓缩(约50重量百分比)混合物不会凝胶化,但在含有低至0.5重量百分比PEG-脂质的混合物中确实会发生凝胶化。当L-α,g状态从流体层状L-α相开始时,其一个决定性特征是层错型缺陷的增殖,这些缺陷通过PEG-脂质向连接膜的高膜曲率缺陷区域的偏析而得以稳定。