Covalently grafting polycation to bacterial cellulose for antibacterial and anti-cell adhesive wound dressings

生物相容性 嫁接 细菌纤维素 纤维素 原子转移自由基聚合 胶粘剂 伤口愈合 化学 抗菌活性 甲基丙烯酸酯 聚合 粘附 表面改性 高分子化学 细菌 有机化学 生物 聚合物 免疫学 图层(电子) 物理化学 遗传学
作者
Kangkang Ou,Yang Liu,Lili Deng,Shiyan Chen,Song Gu,Baoxiu Wang
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:269: 132157-132157 被引量:39
标识
DOI:10.1016/j.ijbiomac.2024.132157
摘要

Hydrogel-based wound dressings are becoming increasingly important for wound healing. Bacterial cellulose (BC) has been commonly used as wound dressings due to its good in vitro and in vivo biocompatibility. However, pure BC does not possess antibacterial properties. In this regard, polycation gel was grafted onto the BC using a surface-initiated activator regenerated by electron transfer atom transfer radical polymerization (SI-ARGET ATRP) with subsequent quaternization for antibacterial wound dressing. Dimethylethyl methacrylate (DMAEMA) was successfully polymerized on the BC surface which was confirmed by Fourier transform infrared spectroscopy and elemental analysis. The morphology structure, specific surface area, pore size, and mechanical properties were also characterized. The quaternized PDMAEMA grafted on the BC endowed it with excellent antibacterial activity against E. coli (Gram-negative) and S. aureus (Gram-positive) with a killing rate of 89.2 % and 93.4 %, respectively. The number of cells was significantly reduced on QPD/BC hydrogel, demonstrating its good anti-adhesion ability. In vitro cellular evaluation revealed that the antibacterial wound dressing exhibited good biocompatibility. Overall, this study provides a feasible method to develop antibacterial and anti-cell adhesive hydrogel, which has a promising potential for wound healing.
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