Antimicrobial properties and toxicity of imidazolium ionic liquids and their complexes with β-cyclodextrin
DOI:
https://doi.org/10.15407/dopovidi2015.03.107Keywords:
antimicrobial properties, ionic liquids, toxicity, β-cyclodextrinAbstract
Water soluble ionic liquid 1-dodecyl-3-methylimidazolium chloride and water resistant ionic liquid 1-dodecyl-3-methylimidazolium tetrafluoroborate have been synthesized. The inclusion complexes of ionic liquids with β-cyclodextrin in a molar ratio of 1 : 1 have been obtained. The structure of the complexes was confirmed by IR-spectroscopy and differential scanning calorimetry. Antimicrobial activity of both ionic liquids and their complexes with β-cyclodextrin has been established against Staphylococcus aureus (ATCC-25923), Escherichia coli (ATCC-25922), Pseudomonas aeruginosa (ATCC-27853), Candida albicans (M 885 ATCC 10231), and Candida albicans (clinical isolate) test-cultures. It is found that the complex formation of ionic liquids with β-cyclodextrin considerably reduces their toxicity.
Downloads
References
Welton T. Chem. Rev., 1999, 99, No 8: 2071–2084. https://doi.org/10.1021/cr980032t
Hong K., Zhang H., Mays J. et al. Chem. Commun., 2002, 13: 1368–1369. https://doi.org/10.1039/b204319j
Naushad M., Alothman Z., Khan A., Ali M. Int. J. Biol. Macromol., 2012, 51, No 4: 555–560. https://doi.org/10.1016/j.ijbiomac.2012.06.020
Shamshina J., Barber P., Rogers R. Expert Opin. Drug Deliv., 2013, 10, No 10: 1367–1381. https://doi.org/10.1517/17425247.2013.808185
Quinn B., Ding Z., Moulton R., Bard A. Langmuir, 2002, 18, No 5: 1734–1742. https://doi.org/10.1021/la011458x
Singh V., Nigam A., Batra A. et al. Int. J. Elechtrochem., 2012, Article ID 165683: 1–17.
Scott M., Rahman M., Brazel C. Eur. Polym. J., 2003, 39, No 10: 1947–1953. https://doi.org/10.1016/S0014-3057(03)00129-0
Dias A., Marceneiro S., Braga M. et al. Acta Biomater., 2012, 3: 1366–1379. https://doi.org/10.1016/j.actbio.2011.10.034
Docherty K., Kulpa C. Green Chem., 2005, 7: 185–189. https://doi.org/10.1039/b419172b
Carson L., Chau P., Earle M. et al. Green Chem., 2009, 11: 492–497. https://doi.org/10.1039/b821842k
Coleman D., Spulak M., Garcia M. T., Gathergood N. Green Chem., 2012, 14: 1350–1356. https://doi.org/10.1039/c2gc16090k
Rogalski M., Modaressi A., Magri P. et al. Int. J. Mol. Sci., 2013, 14: 16638–16655. https://doi.org/10.3390/ijms140816638
Brewster M., Loftsson T. Adv. Drug Del. Rev., 2007, 59: 645–666. https://doi.org/10.1016/j.addr.2007.05.012
Bauer A., Kirby W., Sherris J., Turck M. Am. J. Clin. Pathol., 1966, 45, No 4: 493–496.
Shaliapin H. Rubokhoziaistv. toksikologiia, 2010, 11, No 1(41): 199–206 (in Russian).
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2025 Reports of the National Academy of Sciences of Ukraine

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.