Synthesis and Self-Assembly of Double-Hydrophilic and Amphiphilic Block Glycopolymers

被引:28
|
作者
Adharis, Azis [1 ]
Ketelaar, Thomas [1 ]
Komarudin, Amalina G. [2 ]
Loos, Katja [1 ]
机构
[1] Univ Groningen, Macromol Chem & New Polymer Mat, Zernike Inst Adv Mat, Nijenborgh 4, NL-9747 AG Groningen, Netherlands
[2] Univ Groningen, Mol Microbiol, Groningen Biomol Sci & Biotechnol Inst, Nijenborgh 7, NL-9747 AG Groningen, Netherlands
关键词
CRITICAL MICELLE CONCENTRATION; RADICAL POLYMERIZATION; RAFT POLYMERIZATION; COPOLYMERS; AGGREGATION; POLYSTYRENE; SCAFFOLDS; POLYMERS; WATER;
D O I
10.1021/acs.biomac.8b01713
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
In this report, we present double-hydrophilic block glycopolymers of poly(-hydroxyethyl methacrylate)-b-poly(2(beta-glucosyloxy)ethyl methacrylate) (PHEMA-b-PGEMA) and amphiphilic block glycopolymers of poly(ethyl methacrylate)-b-PGEMA (PEMA-b-PGEMA) synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization. The block glycopolymers were prepared in two compositions of P(H)EMA macro-chain transfer agents (CTAs) and similar molecular weights of PGEMA. Structural analysis of the resulting polymers as well as the conversion of (H)EMA and GEMA monomers were determined by H-1 NMR spectroscopy. Size exclusion chromatography measurements confirmed both P(H)EMA macro-CTAs and block glycopolymers had a low dispersity (D <= 1.5). The synthesized block glycopolymers had a degree of polymerization and a molecular weight up to 222 and 45.3 kg mol(-1), respectively. Both block glycopolymers self-assembled into micellar structures in aqueous solutions as characterized by fluorescence spectroscopy, ultraviolet-visible spectroscopy, and dynamic light scattering experiments.
引用
收藏
页码:1325 / 1333
页数:9
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