Si-C linked oligo(ethylene glycol) layers in silicon-based photonic crystals:: Optimization for implantable optical materials

被引:66
作者
Kilian, Kristopher A.
Boecking, Till
Gaus, Katharina
Gal, Michael
Gooding, J. Justin [1 ]
机构
[1] Univ New S Wales, Sch Chem, Sydney, NSW 2052, Australia
[2] Univ New S Wales, Sch Phys, Sydney, NSW 2052, Australia
[3] Univ New S Wales, Sch Med Sci, Ctr Vasc Res, Sydney, NSW 2052, Australia
基金
澳大利亚研究理事会;
关键词
porous silicon; photonic crystals; self-assembled monolayers; protein resistance; oligo(ethylene glycol);
D O I
10.1016/j.biomaterials.2007.03.014
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Porous silicon has shown potential for various applications in biology and medicine, which require that the material (1) remain stable for the length of the intended application and (2) resist non-specific adsorption of proteins. Here we explore the efficacy of short oligo(ethylene glycol) moieties incorporated into organic layers via two separate strategies in achieving these aims. In the first strategy the porous silicon structure was modified in a single step via hydrosilylation of alpha-oligo (ethylene glycol)-omega-alkenes containing three or six ethylene glycol units. The second strategy employs two steps: (1) hydrosilylation of succinimidyl-10-undecenoate and (2) coupling of an amino hexa(ethylene glycol) species. The porous silicon photonic crystals modified by the two-step strategy displayed greater stability relative to the single step procedure when exposed to conditions of physiological temperature and pH. Both strategies produced layers that resist non-specific adsorption of proteins as determined with fluorescently labelled bovine serum albumin. The antifouling behaviour and greater stability to physiological conditions provided by this chemistry enhances the suitability of porous silicon for biomaterials applications. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3055 / 3062
页数:8
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