Issue 10, 2016

Bacteriophilic tetra-p-guanidinoethyl-calix[4]arene derived polymers. Syntheses and E. coli sequestration studies

Abstract

The antibacterial tetracationic tetra-p-guanidinoethylcalix[4]arene developed by our team has been anchored through bottom-up or top-down pathways to the surface of Merrifield and Wang benzaldehyde resins; the attachment involved either a pyridinium linker or an imine/amine one. The grafting yields were evaluated by elemental analysis through the nitrogen content. Their sequestering properties towards bacteria were evaluated, using E. coli as a model, by capillary electrophoresis (CE) which showed their efficiencies and their bacteriophilic behaviors. All the new materials were compared to two pyridinium-derived Merrifield resins in terms of effective capture, efficiency, and removal coefficients, showing that some of these calixarene-derived resins are good bacteriophilic materials. Confirmation of such behavior has been provided by microscopy.

Graphical abstract: Bacteriophilic tetra-p-guanidinoethyl-calix[4]arene derived polymers. Syntheses and E. coli sequestration studies

Article information

Article type
Paper
Submitted
17 May 2016
Accepted
28 Jun 2016
First published
14 Jul 2016

New J. Chem., 2016,40, 8239-8250

Bacteriophilic tetra-p-guanidinoethyl-calix[4]arene derived polymers. Syntheses and E. coli sequestration studies

F. Lemée, M. Mourer, L. Aranda, I. Clarot and J. Regnouf-de-Vains, New J. Chem., 2016, 40, 8239 DOI: 10.1039/C6NJ01563H

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