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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 |
Files for this record:
| File | Description | Size | Format | |
|---|---|---|---|---|
| design-of-poly-catechol-biodynamers-for-potentiation-of-antibiotic-efficacy-against-drug-resistant-bacteria.pdf | 9,02 MB | Adobe PDF | View/Open |
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