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Physical Hydrogels of Oxidized Polysaccharides and Poly(Vinyl Alcohol) for Wound Dressing Applications

机译:用于伤口敷料的氧化多糖和聚乙烯醇的物理水凝胶

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摘要

Two natural polymers, i.e., cellulose and water soluble pullulan, have been selectively oxidized employing the TEMPO-mediated protocol, to allow the introduction of C6-OOH groups. Thereafter, the composite hydrogels of poly(vinyl alcohol) (PVA) and different content of the oxidized polysaccharides were prepared by the freezing/thawing method. The Fourier transform infrared spectroscopy (FTIR) has been used to discuss the degree of interaction between the hydrogels constituents into the physical network. The homogeneity of the prepared hydrogels as revealed by the SEM show an excellent distribution of the oxidized polysaccharides inside the PVA matrix. The samples exhibit self-healing features, since they quickly recover the initial structure after being subjected to a large deformation. The cell viability was performed for the selected hydrogels, all of them showing promising results. The samples are able to load L-arginine both by physical phenomena, such as diffusion, and also by chemical phenomena, when imine-type bonds are likely to be formed. The synergism between the two constituents, PVA and oxidized polysaccharides, into the physical network, propose these hydrogels for many other biomedical applications.
机译:两种天然聚合物,即纤维素和水溶性支链淀粉,已采用TEMPO介导的方案进行了选择性氧化,以引入C6-OOH基团。之后,通过冷冻/解冻方法制备了聚乙烯醇(PVA)和不同含量的氧化多糖的复合水凝胶。傅里叶变换红外光谱(FTIR)已用于讨论水凝胶成分与物理网络之间的相互作用程度。通过SEM显示所制备的水凝胶的均质性表明,氧化的多糖在PVA基质内的分布极好。样品具有自我修复的特性,因为它们在经受大的变形后可以快速恢复初始结构。对选定的水凝胶进行细胞活力分析,所有结果均显示出良好的前景。当可能形成亚胺型键时,样品既可以通过物理现象(例如扩散)加载,也可以通过化学现象加载L-精氨酸。 PVA和氧化多糖这两种成分之间的协同作用,形成了物理网络,为许多其他生物医学应用提供了这些水凝胶。

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