Amphiphilic Thermoset Elastomers from Metal-Free, Click Crosslinking of PEG-Grafted Silicone Surfactants

被引:15
作者
Rambarran, Talena [1 ]
Gonzaga, Ferdinand [1 ]
Brook, Michael A. [1 ]
Lasowski, Frances [2 ]
Sheardown, Heather [2 ]
机构
[1] McMaster Univ, Dept Chem & Chem Biol, Hamilton, ON L8S 4M1, Canada
[2] McMaster Univ, Dept Chem Engn, Hamilton, ON L8S 4M1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
amphiphilic; click chemistry; poly(ethylene glycol); polymers; silicone; surface chemistry; thermoset elastomers; POLYMER NETWORKS; POLYDIMETHYLSILOXANE; RECOVERY; EXPOSURE; PDMS;
D O I
10.1002/pola.27539
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The hydrophobicity of silicone elastomers can compromise their utility in some biomaterials applications. Few effective processes exist to introduce hydrophilic groups onto a polysiloxane backbone and subsequently crosslink the material into elastomers. This problem can be overcome through the utilization of metal-free click reactions between azidoalkylsilicones and alkynyl-modified silicones and/or PEGs to both functionalize and crosslink silicone elastomers. Alkynyl-functional PEG was clicked onto a fraction of the available azido groups of a functional polysiloxane, yielding azido reactive PDMS-g-PEG rake surfactants. The reactive polymers were then used to crosslink alkynyl-terminated PDMS of different molecular weights. Using simple starting materials, this generic yet versatile method permits the preparation and characterization of a library of amphiphilic thermoset elastomers that vary in their composition, crosslink density, elasticity, hydrogel formation, and wettability. An appropriate balance of PEG length and crosslink density leads to a permanently highly wettable silicone elastomer that demonstrated very low levels of protein adsorption. (c) 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015, 53, 1082-1093
引用
收藏
页码:1082 / 1093
页数:12
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