聚电解质
傅里叶变换红外光谱
明胶
水溶液
无规线圈
高分子
氢键
多糖
高分子化学
化学
化学工程
结晶学
聚合物
有机化学
分子
圆二色性
工程类
生物化学
作者
Svetlana R. Derkach,Nikolay G. Voron’ko,Nina I. Sokolan,Daria S. Kolotova,Yuliya A. Kuchina
标识
DOI:10.1080/01932691.2019.1611437
摘要
The interaction between macromolecular chains of gelatin and anionic polysaccharide sodium alginate during the formation of polyelectrolyte complexes was examined using UV and FTIR spectroscopy. It has been shown that in an aqueous phase, where the pH is slightly higher than the pI of gelatin, complexes are formed through hydrogen bonds as well as electrostatic interactions between two biopolymers. The complex formation is accompanied by a change in the secondary structure of gelatin. At a low weight (w/w) ratio of polysaccharide to gelatin (up to 0.2) a decrease in the share of collagen-like helices and an increase in the share of the random coil conformation of gelatin chains were reported. SEM was used to identify a fundamental distinction between the morphologies of the gelatin hydrogel and the mixed alginate–gelatin hydrogel with a low mass ratio of biopolymers. Spherical formations were found in the structure of the latter that were interpreted as aggregations of complexes.
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