Improved mechanical properties of antimicrobial poly(N-[3-(dimethylaminopropyl)] methacrylamide) hydrogels prepared by free radical polymerization in the presence of cetyltrimethylammonium bromide as a lyotropic liquid crystal template

Cansu Kozbekci Sabah, Bestenur Yalçın, Ceyda Şimşek, Yeşim H. Gürsel, Candan Erbil*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

The poor mechanical strength of the poly(N-[3-(dimethylamino)propyl] methacrylamide) (PDMAPMAAm) hydrogel limits its application as a drug delivery system and antimicrobial agent. In this study, both its morphology and antibacterial effectiveness were controlled through free radical solution polymerization in the presence of cetyltrimethylammonium bromide (CTAB; cationic nonreactive surfactant), forming lyotropic liquid crystal (LLC) mesophases. All the templated reactions proceeded in four different CTAB concentrations with three different concentrations of DMAPMAAm (2.0, 3.0 and 4.0 mol L−1), which were carried out in distilled-deionized water (DDW) using potassium persulfate (KPS) and N,N′-methylenebisacrylamide (BIS) as the initiator and crosslinker, respectively. The pH-dependent phase transition temperature (34 °C at pH 14), compression moduli, antibacterial and diffusion properties, and the effect of the LLC mesophases of CTAB on the hydrogel properties were investigated by mechanical measurements, image analysis, inhibition zone tests, X-ray diffractograms and polarized optical microscopy (POM). It was found that the compression moduli of the templated (T)-PDMAPMAAm hydrogels increased by nearly ten times (from ∼3.0 to 30.0 kPa) compared to that of the isotropic (I) ones. The POM and XRD results before the removal of CTAB exhibited the formation of lamellar and hexagonal mesophases. Further, the inhibition zones showed the ability of the I-PDMAPMAAm hydrogels to reduce the activity of E. coli even in the absence of CTAB, gentamicin (GS) and ciprofloxacin (CF). This was because the quaternary ammonium (QA) groups on the DMAPMAAm units could interact with the bacterial membrane.

Original languageEnglish
Pages (from-to)4156-4166
Number of pages11
JournalSoft Matter
Volume18
Issue number21
DOIs
Publication statusPublished - 5 May 2022

Bibliographical note

Publisher Copyright:
© 2022 The Royal Society of Chemistry.

Funding

We would like to inform that this work was supported by Istanbul Technical University Scientific Research Project Council (38858) and the Scientific and Technological Research Council of Turkey under Project number 115Z876.

FundersFunder number
Istanbul Technical University Scientific Research Project Council38858
Türkiye Bilimsel ve Teknolojik Araştırma Kurumu115Z876

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