Self-assembly of reactive amphiphilic block copolymers as mimetics for biological membranes

被引:129
作者
Taubert, A [1 ]
Napoli, A [1 ]
Meier, W [1 ]
机构
[1] Univ Basel, Dept Chem, CH-4056 Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
D O I
10.1016/j.cbpa.2004.09.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Over the years, polymers have attracted a great deal of interest because they offer a unique platform for the development of materials in fields as diverse as biomedicine and packaging. Many of these purposes use polymers that had been developed for totally different applications. Recently, however, chemical tailoring and molecular and supramolecular control of the chemistry and, thus, the physical and biological response have become a key interest of many researchers. In particular, systems that operate in aqueous media have become an intensely researched field. This is mostly because many devices must be biocompatible, which implies that they have to function in aqueous solutions. Over the past few years, new approaches for mimicking cell surfaces, for generating biocompatible and bioactive drug delivery systems, and for directed targeting have been developed. One recent development is polymeric systems with an enhanced biofunctionality, such as amphiphilic block copolymers that can act as mimetics for biological membranes. Because there are virtually no limits to combinations of monomers, biological and synthetic building blocks, ligands, receptors, and other proteins, polymer hybrid materials show a great promise for applications in biomedicine and biotechnology.
引用
收藏
页码:598 / 603
页数:6
相关论文
共 32 条
[1]   Self-porating polymersomes of PEG-PLA and PEG-PCL: hydrolysis-triggered controlled release vesicles [J].
Ahmed, F ;
Discher, DE .
JOURNAL OF CONTROLLED RELEASE, 2004, 96 (01) :37-53
[2]   Block copolymer assemblies with cross-link stabilization: From single-component monolayers to bilayer blends with PEO-PLA [J].
Ahmed, F ;
Hategan, A ;
Discher, DE ;
Discher, BM .
LANGMUIR, 2003, 19 (16) :6505-6511
[3]   Stimuli-responsive polypeptide vesicles by conformation-specific assembly [J].
Bellomo, EG ;
Wyrsta, MD ;
Pakstis, L ;
Pochan, DJ ;
Deming, TJ .
NATURE MATERIALS, 2004, 3 (04) :244-248
[4]  
Boerakker MJ, 2002, ANGEW CHEM INT EDIT, V41, P4239, DOI 10.1002/1521-3773(20021115)41:22<4239::AID-ANIE4239>3.0.CO
[5]  
2-E
[6]  
Chécot F, 2002, ANGEW CHEM INT EDIT, V41, P1339, DOI 10.1002/1521-3773(20020415)41:8<1339::AID-ANIE1339>3.0.CO
[7]  
2-N
[8]   From supramolecular polymersomes to stimuli-responsive nano-capsules based on poly(diene-b-peptide) diblock copolymers [J].
Chécot, F ;
Lecommandoux, S ;
Klok, HA ;
Gnanou, Y .
EUROPEAN PHYSICAL JOURNAL E, 2003, 10 (01) :25-35
[9]   Cross-linked polymersome membranes: Vesicles with broadly adjustable properties [J].
Discher, BM ;
Bermudez, H ;
Hammer, DA ;
Discher, DE ;
Won, YY ;
Bates, FS .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (11) :2848-2854
[10]   Polymer vesicles [J].
Discher, DE ;
Eisenberg, A .
SCIENCE, 2002, 297 (5583) :967-973