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Merck

Nitric oxide-releasing S-nitrosothiol-modified xerogels.

Biomaterials (2009-06-09)
Daniel A Riccio, Kevin P Dobmeier, Evan M Hetrick, Benjamin J Privett, Heather S Paul, Mark H Schoenfisch
RESUMO

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 approximately 1.31 micromol 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.

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Sigma-Aldrich
Trimethoxymethylsilane, 98%
Sigma-Aldrich
Trimethoxymethylsilane, 95%
Sigma-Aldrich
Trimethoxymethylsilane, purum, ≥98.0% (GC)