Rapid Evaluation of the Antibacterial Activity of Arylene–Ethynylene Compounds
Source abstract
Abstract
A series of oligo(arylene-ethynylene) (1-3 repeat units) compounds functionalized with quaternary ammonium groups was screened for their antibacterial activity in the dark and with activation by long-wavelength (365 nm) UV irradiation. Several of these compounds have effective bactericidal activity (>99.9% killing) at concentrations between 0.01 and 10 μg/mL. Our approach uses flow cytometry to rapidly screen and evaluate the susceptibility of bacterial populations. The rapidity, high information content, and accuracy of this approach make it an extremely valuable method for the study of antibacterial compounds.
Source: openalex_inverted_index · 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
Center for Biomedical Engineering, Department of Chemical & Nuclear Engineering, University of New Mexico, Albuquerque, New Mexico 87131, United States
References (40)
Show source-provided references
1. Arnt L. · Langmuir · 2003 · 19 · 240410.1021/la0268597 ↗
2. Ishitsuka Y. · Biophys. J. · 2005 · 88 · 421A
3. Codling C. E. · J. Antimicrob. Chemother. · 2003 · 51 · 115310.1093/jac/dkg228 ↗
4. Kenawy E. R. · J. Appl. Polym. Sci. · 2006 · 102 · 478010.1002/app.24126 ↗
5. Lin J. · Biotechnol. Prog. · 2002 · 18 · 108210.1021/bp025597w ↗
6. Siddiqui, A.; Schultz, A. K.Antimicrobial polymer latexes derived from unsaturated quaternary ammonium compounds and antimicrobial coatings, sealants, adhesives and elastomers produced from such latexes. U.S. Patent 6,492,445, Dec 10, 2002.
7. Thorsteinsson T. · J. Med. Chem. · 2003 · 46 · 417310.1021/jm030829z ↗
8. Lu L. D. · Langmuir · 2005 · 21 · 1015410.1021/la046987q ↗
9. Chemburu S. · Langmuir · 2008 · 24 · 1105310.1021/la8016547 ↗
10. Corbitt T. S. · Photochem. Photobiol. Sci. · 2009 · 8 · 99810.1039/b902646k ↗
11. Corbitt T. S. · ACS Appl. Mater. Interfaces · 2009 · 1 · 4810.1021/am800096q ↗
12. Wang Y. · Langmuir · 2010 · 26 · 1250910.1021/la102269y ↗
13. Ogawa K. · Langmuir · 2007 · 23 · 454110.1021/la0630108 ↗
14. Ding L. P. · Langmuir · 2009 · 25 · 1374210.1021/la901457t ↗
15. Wang Y. · Langmuir · 2010 · 26 · 1250910.1021/la102269y ↗
16. Tang Y. L. · Langmuir · 2009 · 25 · 2110.1021/la803111b ↗
17. Tang Y. L. · J. Photochem. Photobiol., A · 2009 · 207 · 410.1016/j.jphotochem.2009.03.006 ↗
18. Zhou Z. J. · J. Phys. Chem. Lett. · 2010 · 1 · 320710.1021/jz101088k ↗
19. Tang Y. · Langmuir · 2011 · 27 · 495610.1021/la105018g ↗
20. Steen H. B. · Cytometry · 1981 · 2 · 128
21. Steen H. B. · Cytometry · 1982 · 2 · 24910.1002/cyto.990020409 ↗
22. Boye E. · J. Gen. Microbiol. · 1983 · 129 · 973
23. Vandilla M. A. · Science · 1983 · 220 · 62010.1126/science.6188215 ↗
24. Berney M. · Appl. Environ. Microbiol. · 2007 · 73 · 328310.1128/AEM.02750-06 ↗
25. Chen P. S. · J. Environ. Monit. · 2005 · 7 · 95010.1039/b505224f ↗
26. Berney M. · Water Res. · 2008 · 42 · 401010.1016/j.watres.2008.07.017 ↗
27. Lloyd D. · FEMS Microbiol. Lett. · 1995 · 133 · 110.1111/j.1574-6968.1995.tb07852.x ↗
28. Shapiro H. M. · 200310.1002/0471722731 ↗
29. Accuri_Cytometers, version 1.32, revision A, 2008.
30. Alvarez-Barrientos A. · Clin. Microbiol. Rev. · 2000 · 13 · 16710.1128/CMR.13.2.167 ↗
31. Baena-Ruano S. · Process Biochem. · 2006 · 41 · 116010.1016/j.procbio.2005.12.016 ↗
32. Bar W. · J. Microbiol. Methods · 2009 · 77 · 8510.1016/j.mimet.2009.01.010 ↗
33. Saegeman V. S. M. · Microsc. Microanal. · 2007 · 13 · 1810.1017/S1431927607070079 ↗
34. Shapiro H. M. · Cytometry · 2001 · 43 · 22310.1002/1097-0320(20010301)43:3<223::AID-CYTO1054>3.0.CO;2-R ↗
35. Alekshun M. N. · Cell · 2007 · 128 · 103710.1016/j.cell.2007.03.004 ↗
36. Allegra S. · Appl. Environ. Microbiol. · 2008 · 74 · 781310.1128/AEM.01364-08 ↗
37. Nikaido H. · Microbiol. Mol. Biol. Rev. · 2003 · 67 · 59310.1128/MMBR.67.4.593-656.2003 ↗
38. Mason D. J. · J. Antimicrob. Chemother. · 1995 · 36 · 44110.1093/jac/36.2.441 ↗
39. Mortimer F. C. · Antimicrob. Agents Chemother. · 2000 · 44 · 67610.1128/AAC.44.3.676-681.2000 ↗
40. Wickens H. J. · Antimicrob. Agents Chemother. · 2000 · 44 · 68210.1128/AAC.44.3.682-687.2000 ↗