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Anti-protein and anti-bacterial behavior of amphiphilic silicones
Silicones with improved water-driven surface hydrophilicity and anti-biofouling behavior were achieved when bulk-modified with poly(ethylene oxide) (PEO) -silane amphiphiles of varying siloxane tether length: α-(EtO) Si-(CH ) -oligodimethylsiloxane - -poly(ethylene oxide) -OCH ( = 0, 4, 13, 17, 24,...
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Published in: | Polymer chemistry 2017-09, Vol.8 (34), p.5239-5251 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Silicones with improved water-driven surface hydrophilicity and anti-biofouling behavior were achieved when bulk-modified with poly(ethylene oxide) (PEO) -silane amphiphiles of varying siloxane tether length: α-(EtO)
Si-(CH
)
-oligodimethylsiloxane
-
-poly(ethylene oxide)
-OCH
(
= 0, 4, 13, 17, 24, and 30). A PEO
-silane [α-(EtO)
Si-(CH
)
-PEO
-OCH
] served as a conventional PEO-silane control. To examine anti-biofouling behavior in the absence versus presence of water-driven surface restructuring, the amphiphiles and control were surface-grafted onto silicon wafers and used to bulk-modify a medical-grade silicone, respectively. While the surface-grafted PEO-control exhibited superior protein resistance, it failed to appreciably restructure to the surface-water interface of bulk-modified silicone and thus led to poor protein resistance. In contrast, the PEO-silane amphiphiles, while less protein-resistant when surface-grafted onto silicon wafers, rapidly and substantially restructured in bulk-modified silicone, exhibiting superior hydrophilicity and protein resistance. A reduction of biofilm for several strains of bacteria and a fungus was observed for silicones modified with PEO-silane amphiphiles. Longer siloxane tethers maintained surface restructuring and protein resistance while displaying the added benefit of increased transparency. |
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ISSN: | 1759-9954 1759-9962 |
DOI: | 10.1039/c7py00944e |