Please use this identifier to cite or link to this item: doi:10.22028/D291-47949
Title: Design of Poly-Catechol Biodynamers for Potentiation of Antibiotic Efficacy against Drug-Resistant Bacteria
Author(s): Zeroug-Metz, Lena
Shehu, Kristela
Bassil, Justine
Podlecki, Justin
Sonntag, Philipp
Koch, Marcus
Christoulaki, Anastasia
Buhler, Eric
Hirsch, Anna K. H.
Kraegeloh, Annette
Schneider, Marc
Lee, Sangeun
Language: English
Title: Biomacromolecules
Volume: 27
Issue: 3
Pages: 1949-1968
Publisher/Platform: ACS
Year of Publication: 2026
Free key words: Aromatic Compounds
Bacteria
Hydrocarbons
Polymers
Toxicological Synergy
DDC notations: 500 Science
Publikation type: Journal Article
Abstract: Catechol-modified polymers, such as DOPA-functionalized systems, have recently gained significant interest for a variety of biomedical applications, particularly in their role as antibacterial adjuvants due to their oxidative activity and ability to generate reactive oxygen species (ROS). Current catechol-functionalized polymers, however, often suffer from a restricted number of catechol groups, limited biocompatibility and solubility, and low stability due to the rapid oxidation under physiological conditions. In this study, we developed a water-soluble, biocompatible DOPA-modified biodynamer (DOPA-BD), leveraging the principles of constitutional dynamic chemistry (CDC). DOPA-BD was synthesized via polycondensation of DOPA-hydrazide and the hexaethylene glycol-conjugated carbazole dialdehyde (CA-HG), forming dynamic imine and acylhydrazone linkages between the monomers. As a result of its dynamic covalent backbone, DOPA-BD exhibits biodegradability and undergoes pH-responsive degradation under mildly acidic conditions typically found at infection sites, leading to a more than 3-fold increase in DOPA-hydrazide release compared to physiological pH. Interestingly, driven by CDC, DOPA-BD folds into a nanorod structure with a hydrodynamic diameter of ∼7.8 nm, surrounded by HG chains that offer water solubility and biocompatibility. Moreover, the incorporation of the DOPA-derivative in each repeating unit yields a polymer with exceptionally high catechol content, which remains stable and resistant to oxidation for 72 h in physiological buffer conditions. Regarding its antibacterial applicability, DOPA-BD demonstrated synergistic antibacterial activity with Azithromycin (AZM) against AZM-resistant E. coli, enhancing the antibiotic’s efficacy by 4-fold. Our study indicates that DOPA-BD induces ROS production in the respective bacterial strain, suggesting ROS generation as one of the possible mechanisms contributing to the observed synergy. Overall, DOPA-BD represents a promising alternative strategy to potentiate antibacterial activity against resistant strains, holding strong potential for future antibacterial applications.
DOI of the first publication: 10.1021/acs.biomac.5c02130
URL of the first publication: https://pubs.acs.org/doi/10.1021/acs.biomac.5c02130
Link to this record: urn:nbn:de:bsz:291--ds-479491
hdl:20.500.11880/41933
http://dx.doi.org/10.22028/D291-47949
ISSN: 1526-4602
1525-7797
Date of registration: 29-May-2026
Description of the related object: Supporting Information
Related object: https://pubs.acs.org/doi/suppl/10.1021/acs.biomac.5c02130/suppl_file/bm5c02130_si_001.pdf
Faculty: NT - Naturwissenschaftlich- Technische Fakultät
Department: NT - Pharmazie
Professorship: NT - Prof. Dr. Anna Hirsch
NT - Prof. Dr. Claus-Michael Lehr
NT - Jun.-Prof. PhD. Sangeun Lee
NT - Prof. Dr. Marc Schneider
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes



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