Self-assemblies of amphiphilic homopolymers: synthesis, morphology studies and biomedical applications

被引:73
|
作者
Zhang, Jin [1 ]
Liu, Kelan [1 ]
Muellen, Klaus [2 ]
Yin, Meizhen [1 ]
机构
[1] Beijing Univ Chem Technol, Beijing Lab Biomed Mat, State Key Lab Chem Resource Engn, Key Lab Carbon Fiber & Funct Polymers,Minist Educ, Beijing 100029, Peoples R China
[2] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
DERIVATIZED HYPERBRANCHED POLYGLYCEROLS; FRAGMENTATION CHAIN TRANSFER; ACID) DIBLOCK COPOLYMERS; DENDRITIC STAR POLYMERS; PH-SENSITIVE VESICLES; MULTIPLE MORPHOLOGIES; BLOCK-COPOLYMERS; POLY(AMIDOAMINE) DENDRIMERS; SUPRAMOLECULAR ASSEMBLIES; RAFT POLYMERIZATION;
D O I
10.1039/c5cc03016a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The need for a simplified access to supramolecular assemblies with enhanced tenability has led to the development of amphiphilic homopolymers (APHPs). This feature article highlights recent advances and future trends in APHP design, self-assembly, and biomedical applications. APHP self-assemblies are prepared by two different routes: the "monomer-induced'' method, which polymerizes functional amphiphilic monomers into micelles and inverse micelles, and the "hydrophobic-group-induced'' method, which uses the non-covalent interaction provided by large hydrophobic endgroups. Special emphasis is paid to unimolecular polymeric micelles (UPMs) which are formed from core-shell APHPs and which consist of a hydrophobic/hydrophilic core coated with a polymer shell. The self-assembled supramolecular structures hold promise for various biomedical fields, including living cell transport, fluorescence labelling, protein sensing and extraction, DNA detection, and drug loading and release.
引用
收藏
页码:11541 / 11555
页数:15
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