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

机译:用于伤口敷料应用的氧化多糖和聚(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,即纤维素和水溶性鳞蛋白已被选择性地氧化采用速度介导的方案,以允许引入C6-OOH基团。此后,通过冷冻/解冻方法制备聚(乙烯醇)(PVA)(PVA)(PVA)和氧化多糖的不同含量的复合水凝胶。傅里叶变换红外光谱(FTIR)已被用于讨论水凝胶成分之间的相互作用程度进入物理网络。由SEM揭示的制备水凝胶的均匀性显示出PVA基质内部氧化多糖的优异分布。样品表现出自愈合特征,因为它们在经受大变形后快速恢复初始结构。对选定的水凝胶进行细胞活力,所有这些都显示出有前途的结果。当可能形成亚胺型键时,样品能够通过物理现象(例如扩散),例如扩散,也可以通过化学现象来装载L-精氨酸。两种成分,PVA和氧化多糖之间的协同作用,进入物理网络,提出了许多其他生物医学应用的这些水凝胶。

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