Polymerized ionic liquids-based hydrogels with intrinsic antibacterial activity: Modern weapons against antibiotic-resistant infections

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Authors

  • Johanna Claus
  • Ann Jastram
  • Ewelina Piktel
  • Robert Bucki
  • Paul A. Janmey
  • Udo Kragl

Research Organisations

External Research Organisations

  • Medical University of Bialystok
  • University of Pennsylvania
  • University of Rostock
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Details

Original languageEnglish
Article number50222
JournalJournal of applied polymer science
Volume138
Issue number16
Publication statusPublished - 16 Jan 2021

Abstract

In this study, the inherent antibacterial activity of 11 different polymerized ionic liquids (PILs)-based hydrogels as well as their corresponding monomers was examined in an extensive screening. The methicillin-resistant Staphylococcus aureus Xen 30 (MRSA Xen 30) and Pseudomonas aeruginosa Xen 5 (P. aeruginosa Xen 5) were chosen as test microorganisms. Both are typical representatives of gram-positive and gram-negative bacteria, respectively. Six of the 11 tested monomers were able to eradicate more than 80% of P. aeruginosa Xen 5 cells in suspension. Unfortunately, the anionic, neutral and zwitterionic representatives lost their function after polymerization. However, the cationic gels retained their antibacterial activity with nearly 100% eradication of selected microorganisms - even at the smallest amount tested. Bactericidal activity against gram-positive MRSA Xen 30 was high when the bacteria were treated with the imidazolium-based monomers. Five of the tested compounds showed rather limited bactericidal activity <50% killed bacteria. The weak antibacterial activities could be significantly increased by crosslinking them to three-dimensional networks. As a result, all the hydrogels possessed strong killing efficiencies of at least 68% and were able to maintain this activity even at low hydrogel volume fractions. These findings are very promising for the development of new antibacterial materials for medical applications, for example, stent coatings.

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Polymerized ionic liquids-based hydrogels with intrinsic antibacterial activity: Modern weapons against antibiotic-resistant infections. / Claus, Johanna; Jastram, Ann; Piktel, Ewelina et al.
In: Journal of applied polymer science, Vol. 138, No. 16, 50222, 16.01.2021.

Research output: Contribution to journalArticleResearchpeer review

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abstract = "In this study, the inherent antibacterial activity of 11 different polymerized ionic liquids (PILs)-based hydrogels as well as their corresponding monomers was examined in an extensive screening. The methicillin-resistant Staphylococcus aureus Xen 30 (MRSA Xen 30) and Pseudomonas aeruginosa Xen 5 (P. aeruginosa Xen 5) were chosen as test microorganisms. Both are typical representatives of gram-positive and gram-negative bacteria, respectively. Six of the 11 tested monomers were able to eradicate more than 80% of P. aeruginosa Xen 5 cells in suspension. Unfortunately, the anionic, neutral and zwitterionic representatives lost their function after polymerization. However, the cationic gels retained their antibacterial activity with nearly 100% eradication of selected microorganisms - even at the smallest amount tested. Bactericidal activity against gram-positive MRSA Xen 30 was high when the bacteria were treated with the imidazolium-based monomers. Five of the tested compounds showed rather limited bactericidal activity <50% killed bacteria. The weak antibacterial activities could be significantly increased by crosslinking them to three-dimensional networks. As a result, all the hydrogels possessed strong killing efficiencies of at least 68% and were able to maintain this activity even at low hydrogel volume fractions. These findings are very promising for the development of new antibacterial materials for medical applications, for example, stent coatings.",
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note = "Funding Information: We acknowledge the financial support by the Deutsche Forschungsgemeinschaft and the University of Rostock within the funding programme Open Access Publishing. Funding by the Federal Ministry of Education and Research within RESPONSE “Partnership for Innovation in Implant Technology” (FKZ 03ZZ0910B) and the Deutsche Forschungsgemeinschaft (DFG; grant KR 2491/12‐2) as well as the HERMES research funding of the University of Rostock is gratefully acknowledged. We also thank Katrin Feest for proof reading and Fitzroy Byfield for the technical support.",
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N1 - Funding Information: We acknowledge the financial support by the Deutsche Forschungsgemeinschaft and the University of Rostock within the funding programme Open Access Publishing. Funding by the Federal Ministry of Education and Research within RESPONSE “Partnership for Innovation in Implant Technology” (FKZ 03ZZ0910B) and the Deutsche Forschungsgemeinschaft (DFG; grant KR 2491/12‐2) as well as the HERMES research funding of the University of Rostock is gratefully acknowledged. We also thank Katrin Feest for proof reading and Fitzroy Byfield for the technical support.

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