Self-assemblies of amphiphilic cyclodextrins

被引:92
作者
Roux, Michel [1 ]
Perly, Bruno
Djedaieni-Pilard, Florence
机构
[1] CEA, DSV,iBiTecS, CNRS,URA 2096, Lab Proteines Membranaires, F-91191 Gif Sur Yvette, France
[2] CEA, Serv Chim Mol, DRECAM, F-91191 Gif Sur Yvette, France
[3] Univ Picardie, Lab Glucides, UMR 6219, F-80039 Amiens, France
来源
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS | 2007年 / 36卷 / 08期
关键词
D O I
10.1007/s00249-007-0207-6
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Cyclodextrins are natural cyclic oligosaccharides widely used as "molecular cages" in the pharmaceutical, agrochemical, food and cosmetical industries. The optimization of their pharmacological properties has led to the synthesis of numerous analogues. Amphiphilic derivatives were designed to improve the cell targeting of the drug-containing cyclodextrin cavities through their transportation in the organism, within self-assembling systems. Amphiphilic cyclodextrins can self-assemble into water-soluble aggregates such as mono or polydisperse micelles, or insert in lipid membranes and liposomes. Polysubstituted amphiphilic cyclodextrins are briefly reviewed, and monosubstituted derivatives of native and methylated beta-cyclodextrins are presented in more details, with an emphasis on their self-organization within lipid membranes.
引用
收藏
页码:861 / 867
页数:7
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