Nitric oxide-releasing S-nitrosothiol-modified xerogels

被引:84
作者
Riccio, Daniel A. [1 ]
Dobmeier, Kevin P. [1 ]
Hetrick, Evan M. [1 ]
Privett, Benjamin J. [1 ]
Paul, Heather S. [1 ]
Schoenfisch, Mark H. [1 ]
机构
[1] Univ N Carolina, Dept Chem, Caudill Labs, Chapel Hill, NC 27599 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Nitric oxide; Nitrosothiol; Xerogel; Antithrombotic; Antimicrobial; Cytotoxicity; ANTIBACTERIAL PROPERTIES; PLATELET-ADHESION; IN-VITRO; SOL-GELS; INFECTIONS; NITROSOGLUTATHIONE; MECHANISMS; BLOOD; FLOW; GENERATION;
D O I
10.1016/j.biomaterials.2009.05.006
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The synthesis, material characterization, and in vitro biocompatibility of S-nitrosothiol (RSNO)-modified xerogels are described. Thiol-functionalized xerogel films were formed by hydrolysis and co-condensation of 3-mercaptopropyltrimethoxysilane (MPTMS) and methyltrimethoxysilane (MTMOS) sol-gel precursors at varying concentrations. Subsequent thiol nitrosation via acidified nitrite produced RSNO-modified xerogels capable of generating nitric oxide (NO) for up to 2 weeks under physiological conditions. Xerogels also exhibited NO generation upon irradiation with broad-spectrum light or exposure to copper, with NO fluxes proportional to wattage and concentration, respectively. Xerogels were capable of storing up to similar to 1.31 mu mol NO mg(-1), and displayed negligible fragmentation over a 2-week period. Platelet and bacterial adhesion to nitrosated films was reduced compared to non-nitrosated controls, confirming the antithrombotic and antibacterial properties of the NO-releasing materials. Fibroblast cell viability was maintained on the xerogel surfaces illustrating the promise of RSNO-modified xerogels as biomedical device coatings. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4494 / 4502
页数:9
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