Self-assembly of synthetic glycolipid/water systems

被引:97
|
作者
Hato, M [1 ]
Minamikawa, H [1 ]
Tamada, K [1 ]
Baba, T [1 ]
Tanabe, Y [1 ]
机构
[1] Natl Inst Mat & Chem Res, Dept Polymer Phys, Surface Engn Lab, Tsukuba, Ibaraki 3058565, Japan
关键词
glycolipid; self-assembly; phase behavior; lyotropic liquid crystal; oligosaccharides; stereochemistry; Fd3m reverse micellar cubic phase; H(II) phase; L(alpha) phase;
D O I
10.1016/S0001-8686(98)00085-2
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Glycolipids (amphiphiles that bear oligosaccharides as their hydrophilic headgroups) are of importance both scientifically and technically. This review describes recent advances in our understanding of the molecular correlations in phase behavior in aqueous glycolipids over the past several years. In the first part, we discuss how headgroup stereochemistry affects the phase behavior of glycolipids both in two- and three-dimensional systems. In the second part, we discuss the effects of alkyl chain structure and phase behavior of phytanyl-chained glycolipid/water systems. The physical properties of glycolipid/water systems depend strongly on the inter-headgroup interactions that are related to such factors as stereochemistry (conformation) and size of headgroups, type of sugar residues involved, alkyl chain structure, etc. Thus, apart from the conventional concept like 'hydrophilic/lipophilic balance', explicit accounts of headgroup interactions are crucial to control the particular glycolipid/water system concerned. This is in marked contrast to the conventional amphiphile/water systems where the inter-headgroup interactions are in most cases simply repulsive. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:233 / 270
页数:38
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