pH-Sensitive hydrogels formed by self-assembled amphiphilic triblock copolyelectrolytes

被引:8
|
作者
Charbonneau, Celine [1 ]
Nicolai, Taco [1 ]
Chassenieux, Christophe [1 ]
Colombani, Olivier [1 ]
de Souza Lima, Marli Miriam [1 ,2 ]
机构
[1] Univ Maine, LUNAM Univ, CNRS, IMMM,Dept Polymeres,UMR 6283, F-72085 Le Mans 9, France
[2] Univ Estadual Maringa, Dept Pharm, Lab Phytochem & Technol, BR-5790 Maringa, Parana, Brazil
来源
REACTIVE & FUNCTIONAL POLYMERS | 2013年 / 73卷 / 07期
关键词
Hydrogel; Block copolymer; Self-assembly; Scattering; Rheology; Dynamics; AQUEOUS-SOLUTIONS; BLOCK-COPOLYMERS; GEL; TRANSITION; NETWORKS; MICELLES;
D O I
10.1016/j.reactfunctpolym.2012.12.004
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Results are reviewed of a recent extensive investigation of the behavior of self-assembled pH-sensitive triblock copolymers in aqueous solution. The hydrophilic central block was polyacrylic acid and the two hydrophobic end-blocks were statistical copolymers of n-butyl acrylate and acrylic acid containing 50 mol% acrylic acid units. The hydrophobicity of the end blocks could be modified by changing the degree of ionization of the acrylic acid units (a). The relationship between the pH and a was determined. Scattering techniques showed that flower-like micelles are formed that upon increasing concentration connect via bridging into larger aggregates and above a critical concentration into a percolating network. The rheology of the system is controlled by the exchange rate of the end-blocks between micelles and can be fine-tuned by varying the pH. The exchange rate increases exponentially with increasing a. As a consequence the system changes from a quasi-permanent hydrogel at pH <4.5 to a free flowing liquid at pH > 5.5. The effect of the ionic strength on the structure and the rheology was found to be important only above 0.5 M. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:965 / 968
页数:4
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