Reverse micelles from amphiphilic branched polymers

被引:36
|
作者
Jones, Marie-Christine [2 ]
Leroux, Jean-Christophe [1 ]
机构
[1] ETH, Inst Pharmaceut Sci, Dept Chem & Appl Biosci, CH-8093 Zurich, Switzerland
[2] Univ London, Sch Pharm, London WC1N 1AX, England
关键词
BLOCK-COPOLYMER MICELLES; METAL METHACRYLATE DIBLOCKS; CORE-SHELL ARCHITECTURES; HYPERBRANCHED D-GLUCAN; POLAR GUEST MOLECULES; DRUG-DELIVERY; STAR POLYMERS; PHASE-TRANSFER; MACROMOLECULAR NANOCAPSULE; ENCAPSULATION PROPERTY;
D O I
10.1039/c0sm00272k
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
It is well established that micellar structures can form in non-aqueous solutions. The resulting nanostructures, commonly referred to as 'reverse micelles', are characterized by a polar core and hydrophobic shell. Such micelles have typically been generated from hydrophobically-modified polar branched polymers and evaluated as solubilizing agents for low molecular-weight anionic dyes. From these studies, critical elements, such as micelle composition and size, have been identified as being determinants of micellar behavior. In this manuscript, the synthesis and characterization of amphiphilic branched polymers that have been used in the preparation of reverse micelles are reviewed, with a particular focus on the factors dictating their ability to interact with hydrophilic guest molecules.
引用
收藏
页码:5850 / 5859
页数:10
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