Micelle-Forming and Antimicrobial Properties of a Series of Bis-Quaternized Ammonium Compounds Based on DABCO Derivatives

A set of methods (tensiometry, conductometry, dynamic light scattering, spectroscopy, and fluorimetry) has been employed to study the self-assembly of long-chain bis-quaternized hydroxyethyl group-containing derivatives of 1,4-diazabicyclo[2.2.2]octane. The critical micelle concentrations, adsorption characteristics of the air–water interface, solubilization capacities with respect to poorly water-soluble OrangeOT dye, aggregation numbers, and sizes of aggregates have been determined. The influence of the structure (alkyl chain length and head group charge) of the studied compounds on their micelle-forming and antimicrobial properties, as well as hemolytic activity, has been determined.

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Publication Details

Journal
Colloid Journal
Published
2025-04-01
DOI
https://doi.org/10.1134/s1061933x25600010
Primary Topic
Antimicrobial agents and applications
Type
article
Field-Weighted Citation Impact
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article

Micelle-Forming and Antimicrobial Properties of a Series of Bis-Quaternized Ammonium Compounds Based on DABCO Derivatives

Diana V. Salakhieva, Zukhra Shaihutdinova, A. D. Voloshina, Аnastasiia S. Sapunova et al.
Colloid Journal
Antimicrobial agents and applications
article

Micelle-Forming and Antimicrobial Properties of a Series of Bis-Quaternized Ammonium Compounds Based on DABCO Derivatives

Diana V. Salakhieva, Zukhra Shaihutdinova, A. D. Voloshina, Аnastasiia S. Sapunova, Andrei V. Bogdanov, Tatiana N. Pashirova
article en

Abstract

A set of methods (tensiometry, conductometry, dynamic light scattering, spectroscopy, and fluorimetry) has been employed to study the self-assembly of long-chain bis-quaternized hydroxyethyl group-containing derivatives of 1,4-diazabicyclo[2.2.2]octane. The critical micelle concentrations, adsorption characteristics of the air–water interface, solubilization capacities with respect to poorly water-soluble OrangeOT dye, aggregation numbers, and sizes of aggregates have been determined. The influence of the structure (alkyl chain length and head group charge) of the studied compounds on their micelle-forming and antimicrobial properties, as well as hemolytic activity, has been determined.

Colloid JournalVol. 87(2)
Kazan Federal University (RU), A.E. Arbuzov Institute of Organic and Physical Chemistry (RU)
Openalex Percentile: Top 92%
Antimicrobial agents and applications
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