Kill&Repel Coatings: The Marriage of Antifouling and Bactericidal Properties to Mitigate and Treat Wound Infections
Source abstract
Abstract
Abstract Wound infections originate when exogenous or endogenous bacterial pathogens can circumvent the barrier of the wound dressing and invade the wound bed. Bacterial colonization causes inflammation, stalls the healing process, and carries the risk of dissemination to other tissues. In addition, current antimicrobial dressings fail to resolve an infection once it has been established because debris of the killed bacteria rapidly accumulates on their surface and hampers the antimicrobial action. Faced with this challenge, hybrid synthetic‐natural water‐soluble macromolecules are designed that self‐assemble onto the surface of dressings to generate an antifouling brush functionalized with endolysin, a bactericidal enzyme that poses no harm for eukaryotic cells. The simultaneous action of the brush and the enzyme not only prevents the colonization of the dressing, but also enables the coating to kill planktonic bacteria with even higher efficiency than the free enzyme. Remarkably, the Kill&Repel coating could completely eradicate bacteria in a simulated infection without allowing the adhesion of residues on the surface. Thus, this strategy opens a revolutionary approach for protecting and treating an infected wound in a safer and more efficient manner.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Antimicrobial agents and applications · Antimicrobial Peptides and Activities · Bacterial biofilms and quorum sensing
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
DWI ‐ Leibniz Institute for Interactive Materials Forckenbeckstraße 50 D‐52074 Aachen Germany
Lehrstuhl für Biotechnologie RWTH Aachen University D‐52074 Aachen Germany
Institute of Technical and Macromolecular Chemistry RWTH Aachen University D‐52074 Aachen Germany
Department of Chemistry and Physics of Surfaces and Biointerfaces Institute of Macromolecular Chemistry Czech Academy of Sciences Heyrovsky Square 2 Prague 162 06 Czech Republic
References (51)
Show source-provided references
1. Iqbal A. · World. J. Plast. Surg. · 2017 · 6 · 9
2. 10.1016/j.jval.2017.07.00710.1016/j.jval.2017.07.007 ↗
3. Greulich C. · RSC Adv. · 2012 · 2, 6981
4. 10.1097/PSN.000000000000009610.1097/PSN.0000000000000096 ↗
5. 10.1111/j.1742-481X.2012.00977.x10.1111/j.1742-481X.2012.00977.x ↗
6. 10.1007/s10096-018-3393-510.1007/s10096-018-3393-5 ↗
7. 10.1093/jac/48.1.710.1093/jac/48.1.7 ↗
8. 10.1099/mic.0.27526-010.1099/mic.0.27526-0 ↗
9. 10.1002/anie.20070228710.1002/anie.200702287 ↗
10. 10.1186/s13065-017-0246-810.1186/s13065-017-0246-8 ↗
11. 10.1039/C9MH00291J10.1039/C9MH00291J ↗
12. 10.12968/jowc.2012.21.2.5310.12968/jowc.2012.21.2.53 ↗
13. 10.12968/jowc.1999.8.8.2591010.12968/jowc.1999.8.8.25910 ↗
14. 10.1021/la981356f10.1021/la981356f ↗
15. 10.1163/156856299X0072010.1163/156856299X00720 ↗
16. 10.1016/S0378-4371(97)00293-810.1016/S0378-4371(97)00293-8 ↗
17. 10.1016/S0006-3495(97)78698-310.1016/S0006-3495(97)78698-3 ↗
18. 10.1021/la970678110.1021/la9706781 ↗
19. 10.1002/marc.20110018910.1002/marc.201100189 ↗
20. 10.1002/mabi.20120017110.1002/mabi.201200171 ↗
21. Rodriguez‐Emmenegger C. · WO2016177354 · 2016
22. 10.1039/C3RA43093F10.1039/C3RA43093F ↗
23. 10.1016/j.biomaterials.2007.05.04110.1016/j.biomaterials.2007.05.041 ↗
24. 10.1039/C5PY00197H10.1039/C5PY00197H ↗
25. 10.1039/C4RA12663G10.1039/C4RA12663G ↗
26. 10.1021/bm701293g10.1021/bm701293g ↗
27. 10.1002/anie.20190443610.1002/anie.201904436 ↗
28. 10.1021/acs.macromol.6b0144510.1021/acs.macromol.6b01445 ↗
29. 10.1080/1040869999127924010.1080/10408699991279240 ↗
30. 10.1002/admi.20190084710.1002/admi.201900847 ↗
31. 10.3390/polym1004042310.3390/polym10040423 ↗
32. 10.1002/bit.2718110.1002/bit.27181 ↗
33. 10.1016/j.polymer.2017.03.07010.1016/j.polymer.2017.03.070 ↗
34. Söder D. · Macromol. Biosci. · 2100158
35. 10.2217/fmb.15.810.2217/fmb.15.8 ↗
36. 10.3390/antibiotics1001000910.3390/antibiotics10010009 ↗
37. 10.1007/s00253-006-0771-110.1007/s00253-006-0771-1 ↗
38. 10.1016/S0001-7310(06)73485-810.1016/S0001-7310(06)73485-8 ↗
39. 10.1186/s13104-015-1328-010.1186/s13104-015-1328-0 ↗
40. 10.1016/j.ijmm.2005.11.00110.1016/j.ijmm.2005.11.001 ↗
41. 10.1128/AAC.01933-1510.1128/AAC.01933-15 ↗
42. 10.1007/s15010-007-7251-010.1007/s15010-007-7251-0 ↗
43. 10.1002/marc.20110018910.1002/marc.201100189 ↗
44. 10.1021/acs.biomac.6b0001910.1021/acs.biomac.6b00019 ↗
45. 10.1002/mabi.20170035910.1002/mabi.201700359 ↗
46. 10.1128/JCM.01421-0810.1128/JCM.01421-08 ↗
47. 10.1128/AEM.00829-0610.1128/AEM.00829-06 ↗
48. 10.1021/acscatal.8b0293510.1021/acscatal.8b02935 ↗
49. 10.7717/peerj.2710.7717/peerj.27 ↗
50. 10.1016/j.nantod.2016.05.00610.1016/j.nantod.2016.05.006 ↗
51. 10.1038/nchem.121310.1038/nchem.1213 ↗