2013
DOI: 10.2478/s11658-012-0041-4
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Gemini ester quat surfactants and their biological activity

Abstract: Cationic gemini surfactants are an important class of surface-active compounds that exhibit much higher surface activity than their monomeric counterparts. This type of compound architecture lends itself to the compound being easily adsorbed at interfaces and interacting with the cellular membranes of microorganisms. Conventional cationic surfactants have high chemical stability but poor chemical and biological degradability. One of the main approaches to the design of readily biodegradable and environmentally… Show more

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Cited by 32 publications
(25 citation statements)
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“…The structure of the alanine-derived gemini quaternary ammonium salts (QAS), synthesized at the Department of Chemistry, Technical University of Wroclaw, Poland, as described previously [16] is shown in Fig. 1.
Fig.
…”
Section: Experimental Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…The structure of the alanine-derived gemini quaternary ammonium salts (QAS), synthesized at the Department of Chemistry, Technical University of Wroclaw, Poland, as described previously [16] is shown in Fig. 1.
Fig.
…”
Section: Experimental Methodsmentioning
confidence: 99%
“…To investigate whether the antimicrobial activity depends on the head group structure, a series of gemini QAS (with different alkyl chain and spacer lengths) that mimic alanine was synthesized [16]. In the present study we investigate their biological activity against Gram-positive and Gram-negative bacteria as well as anti-adhesive and biofilm dislodging capacities.…”
Section: Introductionmentioning
confidence: 99%
“…One approach is to introduce an easily cleavable bond into the surfactant structure. Seemingly, for most surfactants containing easily cleavable bonds, the values for ultimate decomposition are higher than those for the corresponding surfactants lacking the weak bond [9] [10]. An important example of such cleavable surfactants is the esterquats, which are surfactants with an ester bond inserted between the polar quaternary ammonium head group and the hydrophobic tail of the surfactant [11].…”
Section: Introductionmentioning
confidence: 99%
“…Estas moléculas desorganizan la disposición normal de la membrana celular o la envoltura de los distintos agentes infecciosos, uniéndose en forma irreversible a los fosfolípidos y las proteínas de esta estructura 86 . De esta manera provocan alteración de su permeabilidad, salida del material vital citoplasmático y la liberación de diversos metabolitos a la célula microbiana que interfieren directamente en su cadena respiratoria o metabolismo energético.…”
Section: Mecanismo De Acciónunclassified