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双重交联多糖磁响应水凝胶的制备:合成、流变性能的调整与评价。

Formulation of Magneto-Responsive Hydrogels from Dually Cross-Linked Polysaccharides: Synthesis, Tuning and Evaluation of Rheological Properties.

机构信息

Department of Physics and Materials Engineering, Faculty of Technology, Tomas Bata University in Zlin, Vavrečkova 275, 760 01 Zlin, Czech Republic.

Centre of Polymer Systems, Tomas Bata University in Zlin, tř. Tomáše Bati 5678, 760 01 Zlin, Czech Republic.

出版信息

Int J Mol Sci. 2022 Aug 25;23(17):9633. doi: 10.3390/ijms23179633.

DOI:10.3390/ijms23179633
PMID:36077030
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9455683/
Abstract

Smart hydrogels based on natural polymers present an opportunity to fabricate responsive scaffolds that provide an immediate and reversible reaction to a given stimulus. Modulation of mechanical characteristics is especially interesting in myocyte cultivation, and can be achieved by magnetically controlled stiffening. Here, hyaluronan hydrogels with carbonyl iron particles as a magnetic filler are prepared in a low-toxicity process. Desired mechanical behaviour is achieved using a combination of two cross-linking routes-dynamic Schiff base linkages and ionic cross-linking. We found that gelation time is greatly affected by polymer chain conformation. This factor can surpass the influence of the number of reactive sites, shortening gelation from 5 h to 20 min. Ionic cross-linking efficiency increased with the number of carboxyl groups and led to the storage modulus reaching 103 Pa compared to 101 Pa-102 Pa for gels cross-linked with only Schiff bases. Furthermore, the ability of magnetic particles to induce significant stiffening of the hydrogel through the magnetorheological effect is confirmed, as a 103-times higher storage modulus is achieved in an external magnetic field of 842 kA·m-1. Finally, cytotoxicity testing confirms the ability to produce hydrogels that provide over 75% relative cell viability. Therefore, dual cross-linked hyaluronan-based magneto-responsive hydrogels present a potential material for on-demand mechanically tunable scaffolds usable in myocyte cultivation.

摘要

基于天然聚合物的智能水凝胶为制造对给定刺激做出即时和可逆反应的响应性支架提供了机会。在心肌细胞培养中,机械特性的调节尤其有趣,可以通过磁控变硬来实现。在这里,通过低毒性工艺制备了具有羰基铁颗粒作为磁性填料的透明质酸水凝胶。使用两种交联途径——动态席夫碱键和离子交联的组合来实现所需的机械性能。我们发现凝胶时间受聚合物链构象的极大影响。这一因素可以超过反应性位点数量的影响,将凝胶时间从 5 小时缩短到 20 分钟。离子交联效率随羧基数量的增加而增加,导致储能模量达到 103 Pa,而仅用席夫碱交联的凝胶储能模量为 101 Pa-102 Pa。此外,通过磁流变效应证实了磁性颗粒对水凝胶产生显著变硬的能力,在 842 kA·m-1 的外部磁场中,储能模量提高了 103 倍。最后,细胞毒性测试证实了能够生产提供超过 75%相对细胞活力的水凝胶的能力。因此,双交联透明质酸基磁响应水凝胶为按需机械可调支架提供了一种有潜力的心肌细胞培养材料。

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