Self-Stratified Antimicrobial Acrylic Coatings via One-Step UV Curing
Source abstract
Abstract
We designed and synthesized a novel quaternary ammonium methacrylate compound (QAC-2) bearing a perfluoroalkyl tail on one end and an acrylic moiety on the other. Via one-step UV curing of QAC-2 and methyl methacrylate (MMA) with ethylene glycol dimethacrylate (EGDMA) as the cross-linker, we obtained cross-linked coatings with excellent antimicrobial property, as demonstrated by the total kill against both Gram-negative Escherichia coli (E. coli) and Gram-positive Staphylococcus epidermidis (S. epidermidis) at a QAC-2 concentration as low as ∼0.06 mol % (∼0.4 wt %) relative to MMA, which was substantially lower than the QAC amount needed in the coatings containing QACs with a hydrocarbon tail. A zone of inhibition test confirmed that the antimicrobial effect was on the basis of contact killing and there was no leaching of antimicrobial species from the cross-linked coating. The high antimicrobial potency in QAC-2-containing films was the consequence of strong surface enrichment of the fluorinated QAC, as confirmed by X-ray photoelectron spectroscopy (XPS).
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Antimicrobial agents and applications · Marine Biology and Environmental Chemistry · Antimicrobial Peptides and Activities
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Georgia Southern University, P.O. Box 8064, Statesboro, Georgia 30460, United States
Department of Biology, Georgia Southern University, P.O. Box 8042, Statesboro, Georgia 30460, United States
Department of Macromolecular Science and Engineering, Case Western Reserve University, Cleveland, Ohio 44106, United States
Funding
National Institute of Food and Agriculture
References (41)
Show source-provided references
1. 10.1002/adfm.20070079310.1002/adfm.200700793 ↗
2. 10.1002/adma.20070109510.1002/adma.200701095 ↗
3. 10.1002/adfm.20110298010.1002/adfm.201102980 ↗
4. 10.1002/adfm.20130168610.1002/adfm.201301686 ↗
5. 10.1021/am401098u10.1021/am401098u ↗
6. 10.1021/cr200350v10.1021/cr200350v ↗
7. 10.1021/la062216610.1021/la0622166 ↗
8. 10.1016/j.progpolymsci.2011.08.00510.1016/j.progpolymsci.2011.08.005 ↗
9. 10.1039/b208575e10.1039/b208575e ↗
10. 10.1021/ja061442z10.1021/ja061442z ↗
11. 10.1038/nmat209910.1038/nmat2099 ↗
12. 10.1002/adma.20030625310.1002/adma.200306253 ↗
13. 10.1039/c0jm00817f10.1039/c0jm00817f ↗
14. 10.1002/app.3192210.1002/app.31922 ↗
15. 10.1016/S0223-5234(03)00059-X10.1016/S0223-5234(03)00059-X ↗
16. 10.1021/am800046r10.1021/am800046r ↗
17. 10.1002/pola.131710.1002/pola.1317 ↗
18. 10.1016/S0032-3861(98)00383-810.1016/S0032-3861(98)00383-8 ↗
19. 10.1002/app.135310.1002/app.1353 ↗
20. 10.1039/b702079a10.1039/b702079a ↗
21. 10.1016/j.porgcoat.2011.05.00610.1016/j.porgcoat.2011.05.006 ↗
22. 10.1016/j.porgcoat.2011.07.00410.1016/j.porgcoat.2011.07.004 ↗
23. 10.1021/bm061236j10.1021/bm061236j ↗
24. 10.1021/bm005549510.1021/bm0055495 ↗
25. 10.1021/ma060762010.1021/ma0607620 ↗
26. 10.1021/la063718m10.1021/la063718m ↗
27. 10.1016/j.memsci.2008.04.01210.1016/j.memsci.2008.04.012 ↗
28. 10.1021/jm030829z10.1021/jm030829z ↗
29. 10.1021/bp050338310.1021/bp0503383 ↗
30. 10.1021/la100153910.1021/la1001539 ↗
31. 10.1021/la063718m10.1021/la063718m ↗
32. 10.1073/pnas.11114309810.1073/pnas.111143098 ↗
33. 10.1021/bm061150q10.1021/bm061150q ↗
34. 10.1016/j.biomaterials.2007.06.01210.1016/j.biomaterials.2007.06.012 ↗
35. 10.1016/j.porgcoat.2011.04.02110.1016/j.porgcoat.2011.04.021 ↗
36. 10.1021/la035307110.1021/la0353071 ↗
37. 10.1021/la049519p10.1021/la049519p ↗
38. Briggs D. · 199810.1017/CBO9780511525261 ↗
39. Kissa, E.Fluorinated Surfactants: Synthesis, Properties, Applications;Marcel Dekker:New York, 1993; p386.
40. 10.1002/pola.2237410.1002/pola.22374 ↗
41. 10.1021/am100018k10.1021/am100018k ↗