Recent developments in iodophor disinfectants.
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Biomedical subjects
Publications and source records attributed to D Mlynarcík.
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The effect of 1-dodecylpiperidine 1-oxide and N,N'-bis(dodecyldimethyl)-1,2-ethane diammonium dibromide on the spores of Bacillus cereus. particularly their binding to intact spores and spores with reduced cystine bonds, was investigated. The Langmuir type of binding is involved in both cases. Both compounds decreased the thermoresistance of spores. DPNO decreased the fraction of non-germinating spores, the effect of the drug increasing with increasing concentration. This phenomenon was associated with a faster release of dipicolinic acid to the medium. Only microgermination proceeded in the presence of BDED and dipicolinic acid was released only in substantially lower amounts. Both compounds also influenced respiration.
Antimicrobial activity of bis-quaternary ammonium salts derived from 1,3-propanediamine and 1,3-diamino-2-propanol is described. Effect of the length of alkyl chain and the substitution in the connecting chain on this activity was studied.
A total of 17 N,N'-dialkyl-N,N'-dimethyl-1,6-hexanediamine dioxides were tested for activity against three microorganisms. A relationship was found between the length of the alkyl substituent and antimicrobial activity.
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A quaternary ammonium salt (1-methyldodecyl)-trimethylammonium iodide, a structurally analogous amine oxide (1-methyldodecyl)-dimethylamine-N-oxide and the amine oxide lacking long alkyl chain trimethylamine-N-oxide were tested for their immunomodulatory activity. Inbred mice strain C57/BL6 were pretreated for 7 days by the compounds under study. The activity of elicited peritoneal macrophages was also tested. Both compounds have a long alkyl chain. In concentrations of 10(-6) M there was a significant increase of the phagocytic, candidacidal and lysozyme activities of the cells. We also observed a suppressed peroxidase activity. The colicidal activity of both the peritoneal and spleen cells were not affected. The amine oxide lacking the long alkyl chain has the same effect at high concentration. A similarity between the effects of the amphiphilic compounds on the macrophages and their antimicrobial efficacy elicits the conclusion that both activities are caused by their ability to interact with the cell membranes.
Antimicrobial activity of N-alkyl-N-dodecylpiperidinium bromides and N-ethyl-N-dodecylheterocycloalkyl ammonium bromides (pyrrolidine, morpholine, perhydroazepine) determined on grampositive and gramnegative bacteria, yeasts and moulds, presented as minimum inhibition concentration (MIC). Comparison of the effect of change of structure: lengthening of alkyl chain, change of heterocyclic ring. Change in the length of alkyl chain markedly affects the antimicrobial activity, change of heterocyclic ring has no substantial effect. The most active compounds were N-heptyl-and N-hexyl-N-dodecylpiperidinium bromides.
Antimicrobial activity of N,N'-bis(decylmethyl)-alpha,omega-alkanediamine dioxides determined on Staphylococcus aureus, Escherichia coli, and Candida albicans is presented as minimal inhibitory concentration (MIC). The effect of the length of linking alkylene chain on this activity has been followed.