4.7 Article

Structure-property relationship of quinuclidinium surfactants-Towards multifunctional biologically active molecules

Journal

COLLOIDS AND SURFACES B-BIOINTERFACES
Volume 140, Issue -, Pages 548-559

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.colsurfb.2015.11.023

Keywords

Cationic surfactants; Quinuclidinium oximes; Biologically active compounds; Structure-property relationship; Crystal structure; Antimicrobial efficacy

Funding

  1. Croatian Ministry of Science [098-0982915-2949]
  2. Croatian Science Foundation [HRZZ-5055]
  3. University of Zagreb

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Motivated by diverse biological and pharmacological activity of quinuclidine and oxime compounds we have synthesized and characterized novel class of surfactants, 3-hydroxyimino quinuclidinium bromides with different alkyl chains lengths (C(n)QNOH; n= 12, 14 and 16). The incorporation of non conventional hydroxyimino quinuclidinium headgroup and variation in alkyl chain length affects hydrophilic-hydrophobic balance of surfactant molecule and thereby physicochemical properties important for its application. Therefore, newly synthesized surfactants were characterized by the combination of different experimental techniques: X-ray analysis, potentiometry, electrical conductivity, surface tension and dynamic light scattering measurements, as well as antimicrobial susceptibility tests. Comprehensive investigation of C(n)QNOH surfactants enabled insight into structure-property relationship i.e., way in which the arrangement of surfactant molecules in the crystal phase correlates with their solution behavior and biologically activity. The synthesized C(n)QNOH surfactants exhibited high adsorption efficiency and relatively low critical micelle concentrations. In addition, all investigated compounds showed very potent and promising activity against Gram-positive and clinically relevant Gram-negative bacterial strains compared to conventional antimicrobial agents: tetracycline and gentamicin. The overall results indicate that bicyclic headgroup with oxime moiety, which affects both hydrophilicity and hydrophobicity of C(n)QNOH molecule in addition to enabling hydrogen bonding, has dominant effect on crystal packing and physicochemical properties. The unique structural features of cationic surfactants with hydroxyimino quinuclidine headgroup along with diverse biological activity have made them promising structures in novel drug discovery. Obtained fundamental understanding how combination of different functionalities in a single surfactant molecule affects its physicochemical properties represents a good starting point for further biological research. (C) 2015 Elsevier B.V. All rights reserved.

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