Abstract
A series of quaternary ammonium compounds that are esters of betaine and fatty alcohols with hydrocarbon chain lengths of 10 to 18 carbon atoms were tested with respect to antimicrobial activities and rates of hydrolysis. When the tetradecyl derivative was tested against some selected microorganisms, the killing effect was comparable to that of the stable quaternary ammonium compound cetyltrimethylammonium bromide. At higher pH values, both the antimicrobial effect and the rate of hydrolysis of the esters increased. However, whereas at pH 6 greater than 99.99% killing of Salmonella typhimurium was achieved with 5 micrograms/ml in 3 min, the rate of hydrolysis was less than 20% in 18 h. At pH 7, a similar killing effect was achieved in 2 min and 50% hydrolysis occurred in ca. 5 h. Thus, it is possible to exploit the rapid microbicidal effect of the compounds before they hydrolyze. The rate of hydrolysis was reduced by the presence of salt. The bactericidal effect of the betaine esters increased with the length of the hydrocarbon chain of the fatty alcohol moiety up to 18 carbon atoms. Since the hydrolysis products are normal human metabolites, the hydrolysis property may extend the use of these quaternary ammonium compounds as disinfectants and antiseptics for food and body surfaces.
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Selected References
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- Ancelin M. L., Vial H. J. Quaternary ammonium compounds efficiently inhibit Plasmodium falciparum growth in vitro by impairment of choline transport. Antimicrob Agents Chemother. 1986 May;29(5):814–820. doi: 10.1128/aac.29.5.814. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ariëns E. J., Simonis A. M. Design of bioactive compounds. Top Curr Chem. 1974;52:1–61. doi: 10.1007/3-540-06873-2_13. [DOI] [PubMed] [Google Scholar]
- Bodor N., Kaminski J. J., Selk S. Soft drugs. 1. Labile quaternary ammonium salts as soft antimicrobials. J Med Chem. 1980 May;23(5):469–474. doi: 10.1021/jm00179a001. [DOI] [PubMed] [Google Scholar]
- Bodor N. Soft drugs: principles and methods for the design of safe drugs. Med Res Rev. 1984 Oct-Dec;4(4):449–469. doi: 10.1002/med.2610040402. [DOI] [PubMed] [Google Scholar]
- Hancock R. E. Alterations in outer membrane permeability. Annu Rev Microbiol. 1984;38:237–264. doi: 10.1146/annurev.mi.38.100184.001321. [DOI] [PubMed] [Google Scholar]
- Isomaa B., Hägerstrand H., Paatero G., Engblom A. C. Permeability alterations and antihaemolysis induced by amphiphiles in human erythrocytes. Biochim Biophys Acta. 1986 Sep 11;860(3):510–524. doi: 10.1016/0005-2736(86)90548-1. [DOI] [PubMed] [Google Scholar]
- METAYER M., JACOB J. Préparation et propriétés pharmacodynamiques de quelques esters de la bétaïne. Ann Pharm Fr. 1952 Jun;10(6):435–440. [PubMed] [Google Scholar]
- Paatero G. I., Brown D. L., Waterhouse P. D. Inhibition of surface immunoglobulin capping on mouse splenic lymphocytes by cetyltrimethylammonium bromide. Cell Mol Biol. 1986;32(1):79–85. [PubMed] [Google Scholar]
- Pinnaduwage P., Schmitt L., Huang L. Use of a quaternary ammonium detergent in liposome mediated DNA transfection of mouse L-cells. Biochim Biophys Acta. 1989 Oct 2;985(1):33–37. doi: 10.1016/0005-2736(89)90099-0. [DOI] [PubMed] [Google Scholar]
- Tachibana H., Yoshihara E., Kaneda Y., Nakae T. In vitro lysis of the bloodstream forms of Trypanosoma brucei gambiense by stearylamine-bearing liposomes. Antimicrob Agents Chemother. 1988 Jul;32(7):966–970. doi: 10.1128/aac.32.7.966. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wollenweber H. W., Broady K. W., Lüderitz O., Rietschel E. T. The chemical structure of lipid A. Demonstration of amide-linked 3-acyloxyacyl residues in Salmonella minnesota Re lipopolysaccharide. Eur J Biochem. 1982 May;124(1):191–198. doi: 10.1111/j.1432-1033.1982.tb05924.x. [DOI] [PubMed] [Google Scholar]
