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Uniform antibacterial cylindrical nanoparticles for enhancing the strength of nanocomposite hydrogels |
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| Authors: | Zehua Li Amanda K Pearce Jianzhong Du Andrew P Dove Rachel K O'Reilly |
| Institution: | 1. Department of Chemistry, University of Warwick, Coventry, UK
School of Chemistry, University of Birmingham, Birmingham, UK Department of Polymeric Materials, School of Materials Science and Engineering, Tongji University, Shanghai, China Contribution: Data curation (lead), Methodology (lead), Writing - original draft (lead);2. School of Chemistry, University of Birmingham, Birmingham, UK Contribution: Data curation (supporting), Supervision (supporting), Writing - original draft (supporting), Writing - review & editing (lead);3. Department of Polymeric Materials, School of Materials Science and Engineering, Tongji University, Shanghai, China;4. School of Chemistry, University of Birmingham, Birmingham, UK |
| Abstract: | Crystallization-driven self-assembly (CDSA) was employed for the preparation of monodisperse cationic cylindrical nanoparticles with controllable sizes, which were subsequently explored for their effect on antibacterial activity and the mechanical properties of nanocomposite hydrogels. Poly(ɛ-caprolactone)-block-poly(methyl methacrylate)-block-poly2-(tert-butylamino) ethyl methacrylate] (PCL-b-PMMA-b-PTA) triblock copolymers were synthesized using combined ring-opening and RAFT polymerizations, and then self-assembled into polycationic cylindrical micelles with controllable lengths by epitaxial growth. The polycationic cylinders exhibited intrinsic cell-type-dependent antibacterial capabilities against gram-positive and gram-negative bacteria under physiological conditions, without quaternization or loading of any additional antibiotics. Furthermore, when the cylinders were combined into anionic alginate hydrogel networks, the mechanical response of the hydrogel composite was tunable and enhanced up to 51%, suggesting that cationic polymer fibers with controlled lengths are promising mimics of the fibrous structures in natural extracellular matrix to support scaffolds. Overall, this polymer fiber/hydrogel nanocomposite shows potential as an injectable antibacterial biomaterial, with possible application in implant materials as bacteriostatic agents or bactericides against various infections. |
| Keywords: | alginate hydrogels antibacterial micelles crystallization-driven self-assembly nanocomposites |