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Fabrication of a self-healing hydrogel with antibacterial activity using host-guest interactions between dopamine-modified alginate and β-cyclodextrin dimer

生物相容性 自愈水凝胶 化学 伤口愈合 抗菌活性 细胞包封 聚合物 控制释放 纳米技术 生物物理学 化学工程 生物医学工程 材料科学 高分子化学 有机化学 细菌 外科 遗传学 工程类 医学 生物
作者
Moslem Sadeghi,Younes Habibi,Tohid Bohlool,Zahra Mohamadnia,Nasser Nikfarjam,Mastaneh Norouzi
出处
期刊:International Journal of Biological Macromolecules [Elsevier]
卷期号:273: 132827-132827 被引量:2
标识
DOI:10.1016/j.ijbiomac.2024.132827
摘要

Self-healing hydrogels possess an ability to recover their functionality after experiencing damage by regenerating cross-links. The main challenge in making self-healing hydrogels based on host-guest (HG) interactions is their limited mechanical strength, which can be solved using beta-cyclodextrin dimers (β-CDsD). Here, β-CDsD as a host cross-linker was used to increase the mechanical property of the HG interactions. Alginate with acceptable biocompatibility was modified by dopamine (ALG-DOP) and employed as a guest polymer. Self-healing hydrogel was developed between them, and Ag nanoparticles were added to create an antibacterial activity. Dopamine with appropriate size and suitable adhesiveness established HG interactions with β-CDsD, and cells were able to grow well on hydrogel. This hydrogel showed an impressive self-healing capability <5 min. These hydrogels revealed a respectable porosity from 15 to 55 μm essential for exchanging the substances required for cell growth and cell waste elimination. Biocompatibility was investigated against NIH 3 T3 fibroblasts cells, and the results showed that the cells grew well. The in vitro release of curcumin from the hydrogel was examined in PBS at pH of 7.4. The hydrogel can be a perfect candidate for controlled drug release, and wound-dressing due to self-healing property, antibacterial activity, adhesion, and biocompatibility.
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