Bioapplications of RAFT Polymerization

被引:886
作者
Boyer, Cyrille [1 ]
Bulmus, Volga [2 ]
Davis, Thomas P. [1 ]
Ladmiral, Vincent [3 ]
Liu, Jingquan [1 ]
Perrier, Sebastien [3 ]
机构
[1] UNSW, Sch Chem Sci & Engn, CAMD, Sydney, NSW 2052, Australia
[2] UNSW, Sch Biotechnol & Biomol Sci, CAMD, Sydney, NSW 2052, Australia
[3] Univ Sydney, Sch Chem, Key Ctr Polymers & Colloids, Sydney, NSW 2006, Australia
关键词
FRAGMENTATION-CHAIN-TRANSFER; LIVING RADICAL POLYMERIZATION; AMPHIPHILIC BLOCK-COPOLYMERS; CROSS-LINKED MICELLES; STRUCTURED POROUS FILMS; WATER-SOLUBLE (CO)POLYMERS; POLYION COMPLEX MICELLES; WELL-DEFINED POLYMERS; IRON-OXIDE NANOPARTICLES; END-GROUP MODIFICATION;
D O I
10.1021/cr9001403
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The bioapplications of reversible addition-fragmentation chain transfer (RAFT) polymerization in biomaterials, drug delivery, gene therapy, glycopolymers, and bioconjugates, are reviewed. RAFT agents are organic compounds possessing a thiocarbonylthio moiety. The structures of the R and Z groups are of critical importance to a successful RAFT polymerization. The R group of a RAFT agent is important in the pre-equilibrium stage of the polymerization. For certain monomers, such as MMA, the ability of a RAFT agent to effectively mediate the polymerization is highly dependent on the nature of the R group, whereas other polymerization systems are more resilient with respect to the R group. Functionalities in RAFT polymers are not limited to the choice of monomers, they can also be introduced by polymeric chain end groups. As RAFT becomes established as a commonplace synthetic technique, it is likely to become a vector that favors interdisciplinary collaborations between polymer groups and research teams focused on bioapplications and within hospitals and medical research institutes.
引用
收藏
页码:5402 / 5436
页数:35
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