Thermoresponsive Polymer-Antibiotic Conjugates Based on Gradient Copolymers of 2-Oxazoline and 2-Oxazine
Park, Jong Ryul, Verderosa, Anthony D., Totsika, Makrina, Hoogenboom, Richard, & Dargaville, Tim R. (2021) Thermoresponsive Polymer-Antibiotic Conjugates Based on Gradient Copolymers of 2-Oxazoline and 2-Oxazine. Biomacromolecules, 22(12), pp. 5185-5194.
Description
A polymer–antibiotic conjugate with thermoresponsive properties near body temperature is presented. The backbone polymer is a copolymer of 2-n-propyl-2-oxazine (PropOzi) and methoxycarbonylethyl-2-oxazoline (C2MestOx) which is conjugated with the broad-spectrum antibiotic, cefazolin, via modification of the methyl ester group of C2MestOx. The resulting polymer–antibiotic conjugate has a cloud point temperature near body temperature, meaning that it can form a homogenous solution if cooled, but when injected into a skin-mimic at 37 °C, it forms a drug depot precipitate. Cleavage of the ester linker leads to quantitative release of the pristine cefazolin (with some antibiotic degradation observed) and redissolution of the polymer. When Escherichia coli were treated with polymer–antibiotic conjugate total clearance is observed within 12 h. The power of this approach is the potential for localized antibiotic delivery, for example, at a specific tissue site or into infected phagocytic cells.
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| ID Code: | 226708 | ||||
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| Item Type: | Contribution to Journal (Journal Article) | ||||
| Refereed: | Yes | ||||
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| Additional Information: | Funding Information: T.R.D. is supported by the ARC Future Fellowship Scheme (no. FT150100408). This work was enabled by the use of the Central Analytical Research Facility hosted by the Institute for Future Environments at QUT and was supported in part by a National Health and Medical Research Council (NHMRC) Project grant (GNT1144046) to M.T. R.H. gratefully acknowledges FWO Flanders and Ghent University for financial support. | ||||
| Measurements or Duration: | 10 pages | ||||
| DOI: | 10.1021/acs.biomac.1c01133 | ||||
| ISSN: | 1525-7797 | ||||
| Pure ID: | 102082601 | ||||
| Divisions: | Current > Research Centres > Centre for Materials Science Current > Research Centres > Centre for Immunology and Infection Control Current > QUT Faculties and Divisions > Faculty of Science Current > Schools > School of Chemistry & Physics Current > QUT Faculties and Divisions > Faculty of Health Current > Schools > School of Biomedical Sciences |
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| Funding Information: | T.R.D. is supported by the ARC Future Fellowship Scheme (no. FT150100408). This work was enabled by the use of the Central Analytical Research Facility hosted by the Institute for Future Environments at QUT and was supported in part by a National Health and Medical Research Council (NHMRC) Project grant (GNT1144046) to M.T. R.H. gratefully acknowledges FWO Flanders and Ghent University for financial support. | ||||
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| Copyright Owner: | 2021 American Chemical Society | ||||
| Copyright Statement: | This work is covered by copyright. Unless the document is being made available under a Creative Commons Licence, you must assume that re-use is limited to personal use and that permission from the copyright owner must be obtained for all other uses. If the document is available under a Creative Commons License (or other specified license) then refer to the Licence for details of permitted re-use. It is a condition of access that users recognise and abide by the legal requirements associated with these rights. If you believe that this work infringes copyright please provide details by email to qut.copyright@qut.edu.au | ||||
| Deposited On: | 01 Dec 2021 14:35 | ||||
| Last Modified: | 04 Jun 2026 14:17 |
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