Sacco Pasquale, Piazza Francesco, Marsich Eleonora, Abrami Michela, Grassi Mario, Donati Ivan
Department of Life Sciences, University of Trieste, Via Licio Giorgieri 5, I-34127 Trieste, Italy.
Department of Medicine, Surgery and Health Sciences, University of Trieste, Piazza dell'Ospitale 1, I-34129 Trieste, Italy.
Gels. 2024 Jan 25;10(2):0. doi: 10.3390/gels10020094.
Agarose is a natural polysaccharide known for its ability to form thermoreversible hydrogels. While the effects of curing temperature and polysaccharide concentration on mechanical properties have been discussed in the literature, the role of ionic strength has been less studied. In the present manuscript, we investigate the effects of supporting salt concentration and the role of cation (i.e. Na or Li, neighbors in the Hofmeister series), on the setting and performance of agarose hydrogels. Compressive and rheological measurements show that the supporting salts reduce the immediate elastic response of agarose hydrogels, with Li showing a stronger effect than Na at high ionic strength, while they significantly increase the extent of linear stress-strain response (i.e., linear elasticity). The presence of increasing amounts of added supporting salt also leads to a reduction in hysteresis during mechanical deformation due to loading and unloading cycles, which is more pronounced with Li than with Na. The combination of rheological measurements and NMR relaxometry shows a mesh size in agarose hydrogels in the order of 6-17 nm, with a thickness of the water layer bound to the biopolymer of about 3 nm. Of note, the different structuring of the water within the hydrogel network due to the different alkali seems to play a role for the final performance of the hydrogels.
琼脂糖是一种天然多糖,以其形成热可逆水凝胶的能力而闻名。虽然文献中已经讨论了固化温度和多糖浓度对机械性能的影响,但离子强度的作用研究较少。在本论文中,我们研究了支持盐浓度的影响以及阳离子(即霍夫迈斯特序列中的相邻离子Na或Li)对琼脂糖水凝胶凝固和性能的作用。压缩和流变学测量表明,支持盐会降低琼脂糖水凝胶的即时弹性响应,在高离子强度下,Li的影响比Na更强,同时它们会显著增加线性应力-应变响应的程度(即线性弹性)。添加的支持盐量增加还会导致由于加载和卸载循环而在机械变形过程中的滞后现象减少,Li比Na更明显。流变学测量和核磁共振弛豫测量相结合表明,琼脂糖水凝胶中的网孔尺寸约为6-17纳米,与生物聚合物结合的水层厚度约为3纳米。值得注意的是,由于不同的碱导致水凝胶网络内水的不同结构似乎对水凝胶的最终性能起作用。