Suppr超能文献

利用霍夫迈斯特效应实现超分子水凝胶的动态自组装

Harnessing the Hofmeister Effect for Dynamic Self-Assembly of Supramolecular Hydrogels.

作者信息

Tang Hongwang, Gao Yuliang, Zhang Jiahao, Li Zhongqi, Gao Qi, Cai Peiwen, Chen Xinyu, Guo Xuhong, van Esch Jan H, Wang Yiming, Xuan Fu-Zhen

机构信息

State Key Laboratory of Chemical Engineering, East China University of Science and Technology, Meilong Road 130, Xuhui, District, Shanghai, 200237, P.R. China.

Department of Chemical Engineering, Delft University of Technology, Van der Maasweg 9, 2629 HZ, Delft, The Netherlands.

出版信息

Angew Chem Int Ed Engl. 2025 Apr 23:e202505417. doi: 10.1002/anie.202505417.

Abstract

Dynamic regulation of intermolecular interactions is essential for the creation of dynamic supramolecular materials with lifelike self-regulating functions. Yet specific ion effect, which is known to possess potent effect on intermolecular interactions, has remained unexplored for such a purpose. Here, we demonstrate our access to dynamic self-assembly of supramolecular hydrogels by orchestrating the Hofmeister effect through a simple enzymatic reaction. The involved gelators containing carboxylate moieties self-assemble into hydrogel (Gel1) at acidic pH and dissolve at basic pH. We surprisingly find that the dissolved gelators at basic pH can be driven to self-assemble into hydrogel (Gel2) by kosmotropic ions through the disruption of gelator-water interactions. By coupling to the enzymatic hydrolysis of urea, Gel1 gradually disintegrates over time because of the production of basic NH. However, interestingly, with the accumulation of kosmotropic ions, NH and CO , the dissolved gelators are driven to self-assemble into Gel2, realizing a self-regulating gel-sol-gel transition process. The transition rate and stiffness of Gel2 are tunable by adjusting the concentrations of urea or urease. This work may shed light on the creation of lifelike self-regulating supramolecular materials using Hofmeister effect for many enticing applications such as ion-programmed biosensing and drug delivery.

摘要

分子间相互作用的动态调节对于创建具有逼真的自我调节功能的动态超分子材料至关重要。然而,已知对分子间相互作用具有强大影响的特定离子效应,尚未针对此目的进行探索。在这里,我们展示了通过简单的酶促反应来调控霍夫迈斯特效应,从而实现超分子水凝胶的动态自组装。所涉及的含有羧酸盐部分的凝胶剂在酸性pH值下自组装成水凝胶(Gel1),在碱性pH值下溶解。我们惊奇地发现,在碱性pH值下溶解的凝胶剂可以通过趋向性离子破坏凝胶剂与水的相互作用,从而被驱动自组装成水凝胶(Gel2)。通过与尿素的酶促水解偶联,由于碱性NH的产生,Gel1会随着时间逐渐分解。然而,有趣的是,随着趋向性离子、NH和CO的积累,溶解的凝胶剂被驱动自组装成Gel2,实现了一个自我调节的凝胶-溶胶-凝胶转变过程。通过调节尿素或脲酶的浓度,可以调节Gel2的转变速率和硬度。这项工作可能为利用霍夫迈斯特效应创建逼真的自我调节超分子材料提供启示,以用于许多诱人的应用,如离子编程生物传感和药物递送。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验