Mechanically strong double network photocrosslinked hydrogels from N,N-dimethylacrylamide and glycidyl methacrylated hyaluronan

被引:157
作者
Weng, Lihui [1 ]
Gouldstone, Andrew [2 ]
Wu, Yuhong [3 ]
Chen, Weiliam [1 ]
机构
[1] SUNY Stony Brook, Dept Biomed Engn, Stony Brook, NY 11794 USA
[2] Northeastern Univ, Dept Mech & Ind Engn, Boston, MA 02115 USA
[3] SUNY Stony Brook, Dept Mat Sci & Engn, Stony Brook, NY 11794 USA
关键词
hyaluronan; N; N-dimethylacrylamide; hydrogels; photocrosslinkable; double network;
D O I
10.1016/j.biomaterials.2008.01.012
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Hyaluronan (HA) is a natural polysaccharide abundant in biological tissues and it can be modified to prepare biomaterials. In this work, HA modified with glycidyl methacrylate was photocrosslinked to form the first network (PHA), and then a series of highly porous PHA/N, N-dimethylacrylamide (DAAm) hydrogels (PHA/DAAm) with high mechanical strength were obtained by incorporating a second network of photocrosslinked DAAm into PHA network. Due to the synergistic effect produced by double network (DN) structure, despite containing, 90% of water, the resulting PHA/DAAm hydrogel showed a compressive modulus and a fracture stress over 0.5 MPa and 5.2 MPa, respectively. Compared to the photocrosslinked hyaluronan single network hydrogel, which is generally very brittle and fractures easily, the PHA/DAAm hydrogels are ductile. Mouse dermal fibroblast was used as a model cell line to validate in vitro non-cytotoxicity of the PHA/DAAm hydrogels. Cells deposited extracellular matrix on the surface of these hydrogels and this was confirmed by positive staining of Type I collagen by Sirius Red. The PHA/DAAm hydrogels were also resistant to biodegradation and largely retained their excellent mechanical properties even after 2 months of co-culturing with fibroblasts. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2153 / 2163
页数:11
相关论文
共 41 条
[1]   Hydrophilic hybrid IPNs of segmented polyurethanes and copolymers of vinylpyrrolidone for applications in medicine [J].
Abraham, GA ;
de Queiroz, AAA ;
San Román, JS .
BIOMATERIALS, 2001, 22 (14) :1971-1985
[2]   EFFECT OF INITIAL TOTAL MONOMER CONCENTRATION ON THE SWELLING BEHAVIOR OF CATIONIC ACRYLAMIDE-BASED HYDROGELS [J].
BAKER, JP ;
HONG, LH ;
BLANCH, HW ;
PRAUSNITZ, JM .
MACROMOLECULES, 1994, 27 (06) :1446-1454
[3]  
Bono Christopher M, 2004, Spine J, V4, p145S, DOI 10.1016/j.spinee.2004.07.005
[4]   The use of physical hydrogels of chitosan for skin regeneration following third-degree burns [J].
Boucard, Nadge ;
Viton, Christophe ;
Agay, Diane ;
Mari, Eliane ;
Roger, Thierry ;
Chancerelle, Yves ;
Domard, Alain .
BIOMATERIALS, 2007, 28 (24) :3478-3488
[5]   Dependency of swelling on the length of subchain in poly(N,N-dimethylacrylamide)-based gels [J].
Bromberg, L ;
Grosberg, AY ;
Matsuo, ES ;
Suzuki, Y ;
Tanaka, T .
JOURNAL OF CHEMICAL PHYSICS, 1997, 106 (07) :2906-2910
[6]  
Bulpitt P, 1999, J BIOMED MATER RES, V47, P152
[7]   Controlled degradation and mechanical behavior of photopolymerized hyaluronic acid networks [J].
Burdick, JA ;
Chung, C ;
Jia, XQ ;
Randolph, MA ;
Langer, R .
BIOMACROMOLECULES, 2005, 6 (01) :386-391
[8]   Tissue engineering-based cartilage repair with allogenous chondrocytes and gelatin-chondroitin-hyaluronan tri-copolymer scaffold: A porcine model assessed at 18, 24, and 36 weeks [J].
Chang, CH ;
Kuo, TF ;
Lin, CC ;
Chou, CH ;
Chen, KH ;
Lin, FH ;
Liu, HC .
BIOMATERIALS, 2006, 27 (09) :1876-1888
[9]   Atom transfer radical polymerization of N,N-dimethylacrylamide [J].
Ding, SJ ;
Radosz, M ;
Shen, YQ .
MACROMOLECULAR RAPID COMMUNICATIONS, 2004, 25 (05) :632-636
[10]   Hydrogels for tissue engineering: scaffold design variables and applications [J].
Drury, JL ;
Mooney, DJ .
BIOMATERIALS, 2003, 24 (24) :4337-4351