Zhang Qun, Yan Yonggan, Li Zhao, Du Jing, Zhang Kai, Zhang Liguo, Wang Ting, Bianco Alberto, Ge Shaohua, Ma Baojin
Department of Periodontology & Tissue Engineering and Regeneration, School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong University & Shandong Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Laboratory for Dental Materials and Oral Tissue Regeneration & Shandong Provincial Clinical Research Center for Oral Diseases, Jinan, Shandong 250012, China.
CNRS, Immunology, Immunopathology and Therapeutic Chemistry, UPR3572, University of Strasbourg, ISIS, Strasbourg 67000, France.
Int J Biol Macromol. 2023 Oct 27:127726. doi: 10.1016/j.ijbiomac.2023.127726.
The controllable crosslinking between the constituting building blocks plays a key role in endowing the hydrogel with injectability through the formation of a uniform 3D interconnected network. Herein, a uniform-unsaturated crosslinking strategy has been devised to quickly construct injectable sodium alginate (SA) hydrogels. Under vigorous stirring, a moderate amount of metal ions can uniformly coordinate with the guluronate moieties of SA molecules, avoiding the locally excessive crosslinking and the loss of injectability caused by traditional dropping and soaking methods. The injectability of SA hydrogels can be regulated by easily adjusting the concentration of metal ions, and 0.2% (w/v) is the optimal concentration of CaCl for the preparation of injectable SA-Ca hydrogel. Meanwhile, multiple metal ions mediated crosslinking also has been achieved conveniently, expanding the functions. Importantly, SA hydrogels can function as the general platform of composites made of various molecules and materials, for targeting drug delivery, tissue repair, wound infection treatment, and so on. Further, injectable SA-0.2%Cu hydrogel as a model to treat wound infections can promote the healing of full-thickness skin. This study provides a super facile and universal strategy to prepare various SA injectable hydrogels with low cost, which hold great potential in biomedical applications and clinical transformation.
构成结构单元之间的可控交联通过形成均匀的三维互连网络,在赋予水凝胶可注射性方面起着关键作用。在此,设计了一种均匀不饱和交联策略,以快速构建可注射的海藻酸钠(SA)水凝胶。在剧烈搅拌下,适量的金属离子可与SA分子的古洛糖醛酸部分均匀配位,避免局部过度交联以及传统滴加和浸泡方法导致的可注射性丧失。SA水凝胶的可注射性可通过轻松调节金属离子浓度来调控,0.2%(w/v)是制备可注射SA-Ca水凝胶时CaCl的最佳浓度。同时,还方便地实现了多种金属离子介导的交联,拓展了功能。重要的是,SA水凝胶可作为由各种分子和材料制成的复合材料的通用平台,用于靶向给药、组织修复、伤口感染治疗等。此外,作为治疗伤口感染模型的可注射SA-0.2%Cu水凝胶可促进全层皮肤愈合。本研究提供了一种超简便且通用的策略,以低成本制备各种SA可注射水凝胶,在生物医学应用和临床转化中具有巨大潜力。