Nitric oxide-releasing S -nitrosothiol-modified xerogels

Abstract 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)...

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Veröffentlicht in:Biomaterials 2009-09, Vol.30 (27), p.4494-4502
Hauptverfasser: Riccio, Daniel A, Dobmeier, Kevin P, Hetrick, Evan M, Privett, Benjamin J, Paul, Heather S, Schoenfisch, Mark H
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Sprache:eng
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Zusammenfassung:Abstract 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 ∼1.31 μmol 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.
ISSN:0142-9612
1878-5905
DOI:10.1016/j.biomaterials.2009.05.006