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Preparation of a Strong Gelatin-Short Linear Glucan Nanocomposite Hydrogel by an in Situ Self-Assembly Process

机译:一种通过原位自组装工艺制备强明胶短直线葡聚糖纳米复合水凝胶

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摘要

Gelatin hydrogels exhibit excellent biocompatibility, nonimmunogenicity, and biodegradability, but they have limited applications in the food and medical industries because of their poor mechanical properties. Herein, we first developed an in situ self-assembly process for the preparation of gelatin-short linear glucan (SLG) nanocomposite hydrogels with enhanced mechanical strength. The microstructure, dynamic viscoelasticity, compression behavior, and thermal characteristics of the gelatin-SLG nanocomposite hydrogels were determined using scanning electron microscopy (SEM), dynamic rheological experiments, compression tests, and texture profile analysis tests. The SEM images revealed that nanoparticles were formed by the in situ self-assembly of SLG in the gelatin matrix and that the size of these nanoparticles ranged between 200 and 600 nm. The pores of the nanocomposite hydrogels were smaller than those of the pure gelatin hydrogels. Transmission electron microscopy images and X-ray diffraction further confirmed the presence of SLG nanoparticles with spherical shapes and B-type structures. Compared with pure gelatin hydrogels, the nanocomposite hydrogels exhibited improved mechanical behavior. Notably, the hardness and maximum values of the compressive stress of gelatin-SLG nanocomposites containing 5% SLG increased by about 2-fold and 3-fold, respectively, compared to the corresponding values of pure gelatin hydrogels.
机译:明胶水凝胶具有出色的生物相容性,非致力性和生物降解性,但由于其机械性能差,它们在食品和医疗行业中具有有限的应用。在此,我们首先开发出原位自组装方法,用于制备具有增强的机械强度的明胶 - 短直链葡聚糖(SLG)纳米复合水凝胶。使用扫描电子显微镜(SEM),动态流变实验,压缩试验和纹理分布分析测试测定明胶-SLG纳米复合水凝胶的微观结构,动态粘弹性,压缩性能和热特性。 SEM图像显示,通过在明胶基质中的SLG的原位自组装形成纳米颗粒,并且这些纳米颗粒的尺寸范围为200至600nm。纳米复合水凝胶的孔小于纯明胶水凝胶的孔。透射电子显微镜图像和X射线衍射进一步证实了具有球形和B型结构的SLG纳米颗粒的存在。与纯明胶水凝胶相比,纳米复合水凝胶表现出改善的机械行为。值得注意的是,与纯明胶水凝胶的相应值相比,含有5%SLG的明胶-SLG纳米复合材料的硬度和最大值分别增加了约2倍和3倍。

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