Su Yingyu, Li Chunyan, Hou Yanwei, Zhao Jingya, Zhao Bingqian, Lu Yanan, Wang Yuxin, Lv Chenxu, Ren Tong, Lv Saifei, Yang Xue, Xue Jintao
College of pharmacy, Xinxiang Medical University, 453003 Xinxiang, PR China.
Experimental Teaching Center of Biology and Basic Medicine, North Henan Medical University, Xinxiang 453003, Henan Province, PR China.
Int J Biol Macromol. 2025 Sep;321(Pt 1):146280. doi: 10.1016/j.ijbiomac.2025.146280. Epub 2025 Jul 23.
In this study, a novel injectable hydrogel, termed as FUA-CS, was developed based on furoic acid-modified chitosan (FUA-CS) and applied to accelerate wound healing. Initially, the gelation precursor, FUA-CS polymer, was synthesized by conjugating furoic acid (FUA) molecules to chitosan (CS) chains through amidation. At a physiological temperature (37 °C), the FUA-CS polymers undergo crosslinking with four-armed polyethylene glycol-maleimide (4-arm PEG-Mal) via Diels-Alder reactions, resulting in the formation of viscoelastic hydrogels. The resulting FUA-CS exhibited several desirable properties, including low cytotoxicity, high swelling ratios, and excellent rheological characteristics. Furthermore, in vitro cell assays provided compelling evidence that the FUA-CS significantly enhanced cell proliferation and migration, playing a crucial role in promoting wound healing. Notably, in vivo studies demonstrated that the FUA-CS exhibited excellent biocompatibility and biodegradability, highlighting its potential as a promising candidate for wound healing applications. Wound repair studies revealed that the FUA-CS effectively stimulated angiogenesis and collagen deposition, thereby significantly accelerating the wound-healing process. Compared to the traditional wound dressings, the FUA-CS improved the gas permeability, enhanced moisture retention, increased biocompatibility, and boosted patient comfort and compliance. Therefore, the FUA-CS as a novel and promising solution in the field of wound care, opening new avenues for the development of more effective wound-healing therapies.
在本研究中,基于糠酸修饰的壳聚糖(FUA-CS)开发了一种新型可注射水凝胶,并将其应用于加速伤口愈合。最初,通过酰胺化将糠酸(FUA)分子与壳聚糖(CS)链共轭合成凝胶化前体FUA-CS聚合物。在生理温度(37°C)下,FUA-CS聚合物通过狄尔斯-阿尔德反应与四臂聚乙二醇-马来酰亚胺(4-arm PEG-Mal)发生交联,形成粘弹性水凝胶。所得的FUA-CS具有多种理想特性,包括低细胞毒性、高溶胀率和优异的流变学特性。此外,体外细胞试验提供了有力证据,表明FUA-CS显著增强细胞增殖和迁移,在促进伤口愈合中起关键作用。值得注意的是,体内研究表明FUA-CS具有优异的生物相容性和生物降解性,突出了其作为伤口愈合应用有前景候选物的潜力。伤口修复研究表明,FUA-CS有效刺激血管生成和胶原蛋白沉积,从而显著加速伤口愈合过程。与传统伤口敷料相比,FUA-CS改善了透气性,增强了保湿性,提高了生物相容性,并提升了患者的舒适度和依从性。因此,FUA-CS作为伤口护理领域一种新型且有前景的解决方案,为开发更有效的伤口愈合疗法开辟了新途径。