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霍夫迈斯特序列中阴离子变化时琼脂水凝胶的动力学冻结流变学

Kinetically Frozen Rheology of Agar-agar Hydrogels Upon a Change of Anions in the Hofmeister Series.

作者信息

Hirtzel Jordana, Ball Vincent

机构信息

INSERM UMR_S 1121, CNRS EMR 7003, « Biomaterials and Bioengineering », Centre de Recherche en Biomédecine de Strasbourg, Université de Strasbourg, 1 rue Eugène Boeckel, Strasbourg, F-67000, France.

出版信息

Macromol Rapid Commun. 2025 Jul;46(14):e2500067. doi: 10.1002/marc.202500067. Epub 2025 Apr 14.

Abstract

Hydrogels are materials in which water is present as the major component in a network of macromolecules, inorganic colloids or low molecular weight organogelators. To tune their viscoelastic properties, they can be crosslinked, making use of their chemical moieties, but most often with cytotoxicity issues. Another approach consists in modifying the intermolecular interactions of the gelator or its interactions with water. In this framework, playing with the nature of the used electrolyte becomes a popular approach. Even if many reports describe the influence of anions or cations in the Hofmeister series on the mechanical properties of hydrogels, very few investigate the possibility of modifying those properties in a reversible manner between two states characteristic of each electrolyte. Herein, it is shown that agar-agar hydrogels prepared in the presence of high ionic strength NaCl or NaSCN display strongly different mechanical properties and that a change in the nature of the electrolyte in the presence of the gel does not significantly change its storage and loss moduli. This lack of reversibility in the time scale of one day or more is shown to be related to the high inaccessibility of the water and ions present in the porous volume after the gel formation.

摘要

水凝胶是一类材料,其中水作为主要成分存在于大分子、无机胶体或低分子量有机凝胶剂构成的网络中。为了调节其粘弹性,可利用其化学基团使其交联,但这往往会带来细胞毒性问题。另一种方法是改变凝胶剂的分子间相互作用或其与水的相互作用。在此框架下,改变所用电解质的性质成为一种常用方法。尽管许多报告描述了霍夫迈斯特序列中的阴离子或阳离子对水凝胶力学性能的影响,但很少有人研究在每种电解质特有的两种状态之间以可逆方式改变这些性能的可能性。本文表明,在高离子强度的氯化钠或硫氰化钠存在下制备的琼脂水凝胶具有截然不同的力学性能,并且在凝胶存在时改变电解质的性质不会显著改变其储能模量和损耗模量。在一天或更长时间尺度上缺乏这种可逆性被证明与凝胶形成后多孔体积中存在的水和离子难以接近有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9113/12272534/af0166467c69/MARC-46-2500067-g004.jpg

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