EventsThe 3rd International Electronic Conference on Biomolecules
Published
This submission belongs to the session 4. Biomaterials Design and Characterization of the event The 3rd International Electronic Conference on Biomolecules
Published date
12 Apr, 2024
Academic Editor
author-avatarMartin Muschol
Citation
Patryk Drejka, Marta Chrószcz-Porębska, Alicja Kazek-Kęsik, Izabela Barszczewska-Rybarek, Antibacterial properties of dental copolymers modified with monomers possessing quaternary ammonium groups, in Proceedings of The 3rd International Electronic Conference on Biomolecules, 23 April–25 April 2024, MDPI: Basel, Switzerland
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Antibacterial properties of dental copolymers modified with monomers possessing quaternary ammonium groups

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1. Department of Physical Chemistry and Technology of Polymers, Faculty of Chemistry, Silesian University of Technology, 44-100, Gliwice, Poland, Poland
2. Department of Inorganic Chemistry, Analytical Chemistry and Electrochemistry, Faculty of Chemistry, Silesian University of Technology, 44-100 Gliwice, Poland, Poland
3. Biotechnology Centre, Silesian University of Technology, 44-100 Gliwice, Poland
4. Department of Physical Chemistry and Technology of Polymers, Faculty of Chemistry,Silesian University of Technology, 44-100, Gliwice, Poland, Poland
Abstract

Introduction: Bacteria such as Streptococcus mutans metabolize sugar consumed by humans to organic acids. These acids demineralize teeth, causing caries. In dental practice, caries is treated by the removal of infected tissue and filling the cavity with dental composite restorative material (DCRM). Modification of DCRM to achieve microbiocidal materials is widely researched in the literature, due to the neglecting antibacterial activity of commercial materials.
This research aimed to characterize antibacterial activity against Staphylococcus aureus and Escherichia coli of common dental copolymers modified with previously synthesized monomers possessing quaternary ammonium groups (QAn+TMXDI, where n is the number of carbon atoms in the N-alkyl substituent: 8, 10, or 12) responsible for their antibacterial activity.

Methods: Two series of copolymers were prepared: 20 wt. % of QAn+TMXDI, 20 wt. % TEGDMA, 20 wt. % UDMA, and 40 wt. % Bis-GMA and 40 wt.% QAn+TMXDI, 20 wt. % TEGDMA, and 40 wt. % Bis-GMA. The bacterial adhesion was tested with disc-like samples, which were immersed in bacteria solution, washed with sterile water, and then, suspensions of bacteria remaining on the surface were prepared and spread on agar plates. Next, bacteria colonies were counted.

Results: Copolymers modified with 20 wt. % of QAn+TMXDI showed antibacterial activity comparable to a reference sample, except for a copolymer with QA8+TMXDI, which showed higher activity than other copolymers. In the case of copolymers with 40 wt. %, a significant increase in antibacterial activity was observed.

Conclusions: Microbiocidal properties of modified copolymers depended on the weight content of QAn+TMXDI and the length of the N-alkyl chain. The higher the QAn+TMXDI content, the higher the antibacterial activity. The N-alkyl substituent had the opposite effect, i.e. the higher the number of carbon atoms in the chain, the lower the antibacterial activity.

Keywords
dental resin
quaternary ammonium
urethane-dimethacrylate
antibacterial properties
copolymerization
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