Photocross-Linked Antimicrobial Amino-Siloxane Elastomers
Source abstract
Abstract
Mechanically robust bulk antimicrobial polymers are one way to address disease transmission via contaminated surfaces. Here, we demonstrate the visible light photo-oxidative cross-linking of amine-containing PDMS using a single-component, solvent-free system where amines have a dual role as antimicrobial functionalities and cross-linking sites. Rose Bengal, a xanthene dye used as a fluorescent stain, is thermally reacted with the polymer to give a solvent-free liquid siloxane that can generate reactive singlet oxygen upon aerobic green light irradiation, coupling the amine functionalities into imine cross-links. Photorheological experiments demonstrate that light intensity is the largest kinetic factor in the photo-oxidative curing of these polymers. Room temperature irradiation under an ambient atmosphere results in free-standing elastic materials with mechanical properties that depend on the amount of Rose Bengal present. An ultimate elongation strain of 117% and Young’s modulus of 2.15 MPa were observed for the highest dye loading, with both mechanical properties found to be higher than those for the same solution-based dye amounts. We demonstrate that the solvent-free nature of the material can be exploited to generate 3D structures using low-temperature deposition as well as direct-write patterning and photolithography on glass substrates. The antimicrobial activity was investigated, with the cross-linked material demonstrating greater efficacy against E. coli (Gram negative) compared with MRSA (Gram positive) bacterial strains and inducing complete cell lysis of incubated CHO-K1 mammalian cells, demonstrating applicability as a mechanically robust single-component antimicrobial elastomer.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Antimicrobial agents and applications · Nanoplatforms for cancer theranostics · Photodynamic Therapy Research Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, 2036 Main Mall, University of British Columbia, Vancouver, British Columbia V6T 1Z1, Canada
Department of Chemistry, 109 Bagley Hall, University of Washington, Seattle, Washington 98195-1700, United States
Department of Chemical and Biological Engineering, 2360 East Mall, University of British Columbia, Vancouver, British Columbia V6T 1Z3, Canada
Funding
Natural Sciences and Engineering Research Council of Canada · National Science Foundation
References (53)
Show source-provided references
1. 10.1128/IAI.01310-1310.1128/IAI.01310-13 ↗
2. 10.1126/science.aaf815610.1126/science.aaf8156 ↗
3. 10.1016/j.ajic.2010.04.19610.1016/j.ajic.2010.04.196 ↗
4. 10.1177/00333549071220020510.1177/003335490712200205 ↗
5. 10.1021/acs.bioconjchem.0c0029710.1021/acs.bioconjchem.0c00297 ↗
6. 10.1021/acsbiomaterials.9b0084910.1021/acsbiomaterials.9b00849 ↗
7. 10.1002/adhm.20140041810.1002/adhm.201400418 ↗
8. 10.1021/acs.chemrev.6b0048610.1021/acs.chemrev.6b00486 ↗
9. 10.1021/acs.biomac.7b0105810.1021/acs.biomac.7b01058 ↗
10. 10.1038/nbt130910.1038/nbt1309 ↗
11. 10.1002/adfm.20130168610.1002/adfm.201301686 ↗
12. 10.1021/bm401440h10.1021/bm401440h ↗
13. 10.1002/adfm.20070079310.1002/adfm.200700793 ↗
14. 10.1021/acsami.7b1623510.1021/acsami.7b16235 ↗
15. 10.1002/adfm.20150238410.1002/adfm.201502384 ↗
16. 10.1016/j.carres.2009.01.02210.1016/j.carres.2009.01.022 ↗
17. 10.1021/acs.chemrev.6b0068710.1021/acs.chemrev.6b00687 ↗
18. 10.1021/bm401128r10.1021/bm401128r ↗
19. 10.1021/acsapm.0c0077810.1021/acsapm.0c00778 ↗
20. 10.1039/C6PY01134A10.1039/C6PY01134A ↗
21. 10.1021/ja00349a00710.1021/ja00349a007 ↗
22. 10.1038/nrc107110.1038/nrc1071 ↗
23. 10.1016/j.jphotochem.2012.07.00910.1016/j.jphotochem.2012.07.009 ↗
24. 10.1016/j.bmc.2009.06.04610.1016/j.bmc.2009.06.046 ↗
25. 10.1007/s10593-014-1481-810.1007/s10593-014-1481-8 ↗
26. 10.1016/j.molliq.2008.11.00710.1016/j.molliq.2008.11.007 ↗
27. 10.1039/c2ob25428j10.1039/c2ob25428j ↗
28. 10.1016/j.dyepig.2006.01.03410.1016/j.dyepig.2006.01.034 ↗
29. 10.1002/app.4501710.1002/app.45017 ↗
30. 10.1016/S0032-3861(97)00283-810.1016/S0032-3861(97)00283-8 ↗
31. 10.1016/S0960-894X(00)00279-110.1016/S0960-894X(00)00279-1 ↗
32. 10.1021/ma402361z10.1021/ma402361z ↗
33. 10.3762/bjoc.12.5310.3762/bjoc.12.53 ↗
34. DeRosa M. C. · Coord. Chem. Rev. · 2002 · 233 · 35110.1016/S0010-8545(02)00034-6 ↗
35. 10.1016/j.polymer.2006.06.01310.1016/j.polymer.2006.06.013 ↗
36. 10.1016/0021-9797(88)90357-810.1016/0021-9797(88)90357-8 ↗
37. 10.1021/cm101157w10.1021/cm101157w ↗
38. 10.1039/C7PY01488K10.1039/C7PY01488K ↗
39. 10.1021/acsbiomaterials.6b0022110.1021/acsbiomaterials.6b00221 ↗
40. 10.1002/(SICI)1097-4628(19970711)65:2<373::AID-APP18>3.0.CO;2-010.1002/(SICI)1097-4628(19970711)65:2<373::AID-APP18>3.0.CO;2-0 ↗
41. 10.1016/j.ijbiomac.2021.03.09210.1016/j.ijbiomac.2021.03.092 ↗
42. 10.1002/adma.20180000110.1002/adma.201800001 ↗
43. Nair B. · Int. J. Toxicol. · 2003 · 22 · 1110.1177/1091581803022S204 ↗
44. 10.1167/iovs.05-073510.1167/iovs.05-0735 ↗
45. Theodossiou T. · Cancer Res. · 2003 · 63 · 1818
46. 10.1002/lsm.1013810.1002/lsm.10138 ↗
47. 10.3390/polym712153210.3390/polym7121532 ↗
48. 10.1007/s00253-010-2920-910.1007/s00253-010-2920-9 ↗
49. 10.1128/CMR.12.1.14710.1128/CMR.12.1.147 ↗
50. 10.1002/cbic.20150022610.1002/cbic.201500226 ↗
51. 10.1021/jacs.7b1269810.1021/jacs.7b12698 ↗
52. 10.1016/0005-2736(73)90143-010.1016/0005-2736(73)90143-0 ↗
53. 10.1039/C7PY00831G10.1039/C7PY00831G ↗