journal article·2014-10

Air-ozonolysis to generate contact active antimicrobial surfaces: Activation of polyethylene and polystyrene followed by covalent graft of quaternary ammonium salts

Tania Fadida, Yulia Kroupitski, Uri M. Peiper, Tatyana Bendikov, Shlomo Sela (Saldinger), Elena Poverenov

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Abstract

Air-ozonolysis was revealed as an accessible and effective approach for surface activation and further functionalization of hydrocarbon polymers. Antimicrobial contact active polyethylene (PE) and polystyrene (PS) were designed by generation on their surfaces OH-functional groups and covalent graft of dimethyloctadecyl [3-(trimethoxysilyl) propyl] ammonium chloride (C18-TSA) quaternary ammonium salt. The shortened analog, trimethyl [3-(trimethoxysilyl) propyl] ammonium chloride (C1-TSA), was also covalently attached to the activated PE and PS surfaces. X-ray photoelectron spectroscopy (XPS) and FTIR confirmed the surface modifications. Scanning electron (SEM) and confocal microscopy were utilized to monitor surface morphology and bacteria interactions. The antimicrobial effect of the C18-TSA grafted polymer surfaces was demonstrated on Gram-negative and Gram-positive bacteria species including human pathogen, Salmonella enterica. The shorter C1-TSA grafted polymers did not demonstrate bactericidal activity, suggesting the critical role of the alkyl chain length. The described strategy may establish a new general and safe platform for future development and application of contact active antimicrobial polymers.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Antimicrobial agents and applications · Polymer Surface Interaction Studies · Pharmaceutical and Antibiotic Environmental Impacts

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (37)

Show source-provided references
1. Costerton · Science · 1999 · 284 · 131810.1126/science.284.5418.1318 ↗
2. Campoccia · Biomaterials · 2013 · 34 · 853310.1016/j.biomaterials.2013.07.089 ↗
3. Tiller · Proc. Natl. Acad. Sci. U.S.A. · 2001 · 98 · 598110.1073/pnas.111143098 ↗
4. Larson · Annu. Rev. Chem. Biomol. Eng. · 2013 · 4 · 17110.1146/annurev-chembioeng-061312-103253 ↗
5. Wischerhoff · Adv. Polym. Sci. · 2011 · 240 · 1
6. Fuchs · Angew. Chem. Int. Ed. · 2006 · 45 · 675910.1002/anie.200602738 ↗
7. Madkour · Langmuir · 2009 · 25 · 106010.1021/la802953v ↗
8. Lee · Biomacromolecules · 2004 · 5 · 87710.1021/bm034352k ↗
9. Siedenbiedel · Polymers · 2012 · 4 · 4610.3390/polym4010046 ↗
10. Bower · Colloids Surf. B: Biointerfaces · 2002 · 25 · 8110.1016/S0927-7765(01)00318-6 ↗
11. Ivanov · ACS Appl. Mater. Interfaces · 2012 · 4 · 589110.1021/am301530a ↗
12. Campoccia · Biomaterials · 2013 · 34 · 853310.1016/j.biomaterials.2013.07.089 ↗
13. Ahluwalia · 2012
14. Deng · Prog. Polym. Sci · 2009 · 34 · 15610.1016/j.progpolymsci.2008.06.002 ↗
15. Bilek · Biophys. Rev. · 2010 · 2 · 5510.1007/s12551-010-0028-1 ↗
16. Shard · Macromolecules · 1992 · 25 · 205310.1021/ma00033a034 ↗
17. Davidson · Surf. Sci. · 2005 · 581 · 16910.1016/j.susc.2005.02.049 ↗
18. Popov · J. Polym. Sci., Polym. Phys. Ed. · 1983 · 21 · 101710.1002/pol.1983.180210703 ↗
19. Ton-That · Langmuir · 2000 · 16 · 505410.1021/la9908586 ↗
20. Choi · Nat. Protoc. · 2006 · 1 · 15310.1038/nprot.2006.24 ↗
21. The device which is patented in many countries, including Israel, USA and Europe, is based on an invention by Uri M. Peiper et al. at the Institute for Agricultural Engineering (ARO) and further developed by Sterilion Ltd., a start-up company owned mainly by the inventors.
22. Gilbert · J. Appl. Microbiol. · 2005 · 99 · 70310.1111/j.1365-2672.2005.02664.x ↗
23. Gottenbos · Biomaterials · 2002 · 23 · 141710.1016/S0142-9612(01)00263-0 ↗
24. Li · Langmuir · 2006 · 22 · 982010.1021/la0622166 ↗
25. Oosterhof · Appl. Environ. Microbiol. · 2006 · 72 · 367310.1128/AEM.72.5.3673-3677.2006 ↗
26. Saif · Langmuir · 2008 · 25 · 37710.1021/la802878p ↗
27. Song · Text. Res. J. · 2011 · 81 · 50410.1177/0040517510380776 ↗
28. Yudovin-Farber · Biomacromolecules · 2008 · 9 · 304410.1021/bm8004897 ↗
29. Okahata · Langmuir · 1986 · 2 · 53810.1021/la00070a028 ↗
30. Poverenov · Colloids Surf. B: Biointerfaces · 2013 · 112 · 35610.1016/j.colsurfb.2013.07.032 ↗
31. Gulino · Anal. Bioanal. Chem. · 2013 · 405 · 147910.1007/s00216-012-6394-8 ↗
32. Lupo · J. Phys. Chem. C · 2009 · 113 · 1553310.1021/jp902857g ↗
33. Practical surface analysis
34. Beamson · 1992
35. Brena · Phys. Rev. B · 2004 · 70 · 195214(6)10.1103/PhysRevB.70.195214 ↗
36. Popelka · Molecules · 2012 · 17 · 76210.3390/molecules17010762 ↗
37. Hossain · J. Appl. Polym. Sci. · 2006 · 102 · 145210.1002/app.24308 ↗