Biocompatible, hyaluronic acid modified silicone elastomers

被引:60
作者
Alauzun, Johan G. [1 ,2 ]
Young, Stuart [2 ]
D'Souza, Renita [1 ,2 ]
Liu, Lina [2 ]
Brook, Michael A. [1 ]
Sheardown, Heather D. [2 ]
机构
[1] McMaster Univ, Dept Chem, Hamilton, ON L8S 4M1, Canada
[2] McMaster Univ, Dept Chem Engn, Hamilton, ON L8S 4L7, Canada
关键词
Hyaluronic acid; Poly(dimethylsiloxane) elastomer; Protein adsorption; Cell interactions; Tosyl-modified poly-(ethylene glycol); CROSS-LINKED HYDROGELS; PROTEIN ADSORPTION; DRY EYE; BIOMEDICAL APPLICATIONS; CHONDROITIN SULFATE; ARTIFICIAL TEARS; SURFACE; IMMOBILIZATION; ADHESION; CHAIN;
D O I
10.1016/j.biomaterials.2010.01.069
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Although silicones possess many useful properties as biomaterials, their hydrophobicity can be problematic. To a degree, this issue can be addressed by surface modification with hydrophilic polymers such as poly(ethylene glycol), but the resulting structures are usually not conducive to cell growth. In the present work, we describe the synthesis and characterization of covalently linked hyaluronic acid (HA) (35 kDa) to poly(dimethylsiloxane) (PDMS) elastomer surfaces. HA is of interest because of its known biological properties; its presence on a surface was expected to improve the biocompatibility of silicone materials for a wide range of bioapplications. HA was introduced with a coupling agent in two steps from high-density, tosyl-modified, poly(ethylene glycol) tethered silicone surfaces. All materials synthesized were characterized by water contact angle, ATR-FTIR, XPS and C-13 solid state NMR spectroscopy. Biological interactions with these modified silicone surfaces were assessed by examining interactions with fibrinogen as a model protein as well as determining the in vitro response of fibroblast (3T3) and human corneal epithelial cells relative to unmodified poly(dimethylsiloxane) controls. The results suggest that HA modification significantly enhances cell interactions while decreasing protein adsorption and may therefore be effective for improving biocompatibility of PDMS and other materials. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3471 / 3478
页数:8
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