High porosity, responsive hydrogel copolymers from emulsion templating

被引:59
作者
Ovadia, Maya [1 ]
Silverstein, Michael S. [1 ]
机构
[1] Technion Israel Inst Technol, Dept Mat Sci & Engn, IL-32000 Haifa, Israel
基金
以色列科学基金会;
关键词
polyHIPE; hydrogel; responsive; swelling; emulsion-templating; ionic polymer; SEMIINTERPENETRATING POLYMER NETWORKS; EQUILIBRIUM SWELLING BEHAVIOR; INTERNAL PHASE EMULSIONS; POROUS POLYMERS; CONTROLLED-RELEASE; POLYHIPE; SCAFFOLDS; SYSTEMS; HIPES; FOAMS;
D O I
10.1002/pi.5052
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Hydrogels, three-dimensional hydrophilic polymer network structures, can absorb many times their dry weight in water. PolyHIPEs are highly porous polymers synthesized within high internal phase emulsions (HIPEs). Here, the water uptakes in novel hydrogel polyHIPE copolymers of hydroxyethyl methacrylate (HEMA, a non-ionic monomer) and methacrylic acid (MAA, an ionic monomer) were investigated. The PHEMA-based polyHIPE had a density of 0.14 g cm(-3), void diameters of 50-100 mu m and a void-dominated Fickian water uptake of around 10.4 g g(-1). The polyHIPE density increased, and the porous structure became less polyHIPE-like, with increasing MAA content, reflecting a reduction in the stability of the HIPE. The water uptake increased with increasing pH for all the copolymers and the water absorption mechanism changed from Fickian at pH 2 to anomalous, dominantly case II, at pH 10. The maximum uptake of 18.2 g g(-1) at pH 10, for a HEMA to MAA mass ratio of 1/1, was ascribed to hydrogel-swelling-driven void expansion. The hydrogel's absorptive and responsive properties were amplified by the polyHIPE's porous structure. These results demonstrate that the compositions of hydrogel polyHIPE copolymers can be designed to enhance their water uptake. (c) 2015 Society of Chemical Industry
引用
收藏
页码:280 / 289
页数:10
相关论文
共 60 条
[1]  
Andrews R.J., 1999, Polymer Handbook, V4th, P193
[2]   Surface-initiated RAFT polymerization of NIPAM from monolithic macroporous polyHIPE [J].
Audouin, Fabrice ;
Heise, Andreas .
EUROPEAN POLYMER JOURNAL, 2013, 49 (05) :1073-1079
[3]   Protein Immobilization onto Poly(acrylic acid) Functional Macroporous PolyHIPE Obtained by Surface-Initiated ARGET ATRP [J].
Audouin, Fabrice ;
Larragy, Ruth ;
Fox, Mary ;
O'Connor, Brendan ;
Heise, Andreas .
BIOMACROMOLECULES, 2012, 13 (11) :3787-3794
[4]   Preparation, Solid-State NMR, and Physicochemical Characterization of Surprisingly Tough Open Cell PolyHIPEs Derived from 1-Vinyl-1,2,4-triazole Oil-in-Water Emulsions [J].
Audouin, Fabrice ;
Birot, Marc ;
Pasquinet, Eric ;
Besnard, Olivier ;
Palmas, Pascal ;
Poullain, Didier ;
Deleuze, Herve .
MACROMOLECULES, 2011, 44 (12) :4879-4886
[5]   Responsive polymers in controlled drug delivery [J].
Bajpai, A. K. ;
Shukla, Sandeep K. ;
Bhanu, Smitha ;
Kankane, Sanjana .
PROGRESS IN POLYMER SCIENCE, 2008, 33 (11) :1088-1118
[6]   Tailoring the porosity and morphology of gelatin-methacrylate polyHIPE scaffolds for tissue engineering applications [J].
Barbetta, A ;
Dentini, M ;
Zannoni, EM ;
De Stefano, ME .
LANGMUIR, 2005, 21 (26) :12333-12341
[7]   Scaffolds based on biopolymeric foams [J].
Barbetta, A ;
Dentini, M ;
De Vecchis, MS ;
Filippini, P ;
Formisano, G ;
Caiazza, S .
ADVANCED FUNCTIONAL MATERIALS, 2005, 15 (01) :118-124
[8]   Enzymatic cross-linking versus radical polymerization in the preparation of gelatin polyHIPEs and their performance as scaffolds in the culture of hepatocytes [J].
Barbetta, Andrea ;
Massimi, Mara ;
Devirgiliis, Laura Conti ;
Dentini, Mariella .
BIOMACROMOLECULES, 2006, 7 (11) :3059-3068
[9]   Surface modification of monolithic PolyHIPE Polymers for anionic functionality and their ion exchange behavior [J].
Barlik, Necla ;
Keskinler, Bulent ;
Kocakerim, M. Muhtar ;
Akay, Galip .
JOURNAL OF APPLIED POLYMER SCIENCE, 2015, 132 (29)
[10]   DYNAMIC AND EQUILIBRIUM SWELLING BEHAVIOR OF PH-SENSITIVE HYDROGELS CONTAINING 2-HYDROXYETHYL METHACRYLATE [J].
BRANNONPEPPAS, L ;
PEPPAS, NA .
BIOMATERIALS, 1990, 11 (09) :635-644