Antimicrobial properties and toxicity of imidazolium ionic liquids and their complexes with β-cyclodextrin

TitleAntimicrobial properties and toxicity of imidazolium ionic liquids and their complexes with β-cyclodextrin
Publication TypeJournal Article
Year of Publication2015
AuthorsHodyna, DM, Kobrina, LV, Kalashnikova, LE, Metelytsia, LO, Rogalsky, SP, Tarasyuk, OP, Riabov, SV, Laptiy, SV
Abbreviated Key TitleDopov. Nac. akad. nauk Ukr.
DOI10.15407/dopovidi2015.03.107
Issue3
SectionChemistry
Pagination107-113
Date Published3/2015
LanguageUkrainian
Abstract

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.

Keywordsantimicrobial properties, ionic liquids, toxicity, β-cyclodextrin
References: 

1. Welton T. Chem. Rev., 1999, 99, No 8: 2071–2084. https://doi.org/10.1021/cr980032t
2. Hong K., Zhang H., Mays J. et al. Chem. Commun., 2002, 13: 1368–1369. https://doi.org/10.1039/b204319j
3. 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
4. Shamshina J., Barber P., Rogers R. Expert Opin. Drug Deliv., 2013, 10, No 10: 1367–1381. https://doi.org/10.1517/17425247.2013.808185
5. Quinn B., Ding Z., Moulton R., Bard A. Langmuir, 2002, 18, No 5: 1734–1742. https://doi.org/10.1021/la011458x
6. Singh V., Nigam A., Batra A. et al. Int. J. Elechtrochem., 2012, Article ID 165683: 1–17.
7. 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
8. Dias A., Marceneiro S., Braga M. et al. Acta Biomater., 2012, 3: 1366–1379. https://doi.org/10.1016/j.actbio.2011.10.034
9. Docherty K., Kulpa C. Green Chem., 2005, 7: 185–189. https://doi.org/10.1039/b419172b
10. Carson L., Chau P., Earle M. et al. Green Chem., 2009, 11: 492–497. https://doi.org/10.1039/b821842k
11. Coleman D., Spulak M., Garcia M. T., Gathergood N. Green Chem., 2012, 14: 1350–1356. https://doi.org/10.1039/c2gc16090k
12. Rogalski M., Modaressi A., Magri P. et al. Int. J. Mol. Sci., 2013, 14: 16638–16655. https://doi.org/10.3390/ijms140816638
13. Brewster M., Loftsson T. Adv. Drug Del. Rev., 2007, 59: 645–666. https://doi.org/10.1016/j.addr.2007.05.012
14. Bauer A., Kirby W., Sherris J., Turck M. Am. J. Clin. Pathol., 1966, 45, No 4: 493–496.
15. Shaliapin H. Rubokhoziaistv. toksikologiia, 2010, 11, No 1(41): 199–206 (in Russian).