两亲性
自愈水凝胶
胶束
化学
超分子化学
肽
药物输送
自组装
生物物理学
组合化学
化学工程
高分子化学
水溶液
有机化学
分子
共聚物
生物化学
聚合物
生物
工程类
作者
Xiangyi Liu,Lulu Du,Jia Liu,Yueting Shi,Qipeng Liu,Ying Xu,Yingying Xia,X. Wang,Dan Ding,Xingyi Li,Deqing Lin
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2024-12-02
卷期号:26 (1): 258-265
被引量:1
标识
DOI:10.1021/acs.biomac.4c01050
摘要
With the advantages of less invasiveness and better shape adaptability, in situ-forming hydrogels are desired biomaterials as scaffolds, drug carriers, and so on. Herein, a negatively charged NaCl-responsive ultrashort peptide sequence (EEH) is reported whose electrostatic repulsion can be reduced through the charge-shielding effect. Under physiological conditions, its AIEgen-capped amphiphile TPE-GEEH of low concentration (1 mg/mL) presents NaCl-triggered morphological transformation from micelle to closely packed fiber with enhanced emission, which can be applied to biosense sodium ion (Na+) with high sensitivity and quick response. At a slightly acidic pH, 10 mg/mL TPE-GEEH undergoes sol–gel transition upon addition of NaCl (100 mM) with improved mechanical properties, which should be useful to develop an in situ-forming hydrogel. Overall, our report provides a simple strategy to construct NaCl-responsive assemblies for potential application in biosensors and drug delivery system.
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