Structurally Adjustable Eugenyl-Based Quaternary Phosphonium Cation Degradable Antibacterial Nanomaterials via RAFT
In this study, using bio-based eugenol as the basic polymerization unit, the directional coupling of quaternary phosphonium cations and eugenol was achieved through covalent bonding, and a new type of degradable antibacterial monomer (Eu-PH) was successfully synthesized. Notably, cubic nanoparticles were obtained via the self-assembly of Eu-PH during its homopolymerization, whereas spherical nanoparticles were generated when Eu-PH was copolymerized with <i>N</i>-vinylpyrrolidone (NVP). This structural transformation not only induced significant changes in the material's physicochemical properties but also markedly enhanced its antibacterial efficacy. Experimental results demonstrated that PH<sub><i>x</i></sub>-PVP<sub><i>y</i></sub> achieved inhibition rates of 100% against <i>Escherichia coli</i> and <i>Staphylococcus aureus</i>, with a relative biocompatibility of 99% toward L-929 cells. In addition, PH<sub><i>x</i></sub>-PVP<sub><i>y</i></sub> exhibited excellent degradability and fruit preservation performance. In brief, by virtue of structural regulation of bio-based eugenol and NVP, a promising new approach is proposed for the development of antibacterial materials that simultaneously possess high antibacterial activity, good biocompatibility, and satisfactory degradability.
Authors
- Ruixue Wang (ORCID: https://orcid.org/0000-0002-8772-4954)
- Xingcan Sun
- Xiaobing Ma
- Pengfei Song
- Hailin Cong (ORCID: https://orcid.org/0000-0001-9044-1376)
- Yufeng He
Institutions
- Shandong University of Technology (CN)
- Ministry of Education of the People's Republic of China (CN)
- Ministry of Education (IR)
- Ministry of Education (BD)
- Zaozhuang University (CN)
- Northwest Normal University (CN)
Publication Details
- Journal
- ACS Macro Letters
- Published
- 2026-01-29
- DOI
- https://doi.org/10.1021/acsmacrolett.5c00756
- Primary Topic
- Antimicrobial agents and applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00