Tuneable Transient Thermogels Mediated by a pH- and Redox-Regulated Supramolecular Polymerization

被引:98
|
作者
Spitzer, Daniel [1 ]
Rodrigues, Leona Lucas [1 ]
Strassburger, David [1 ]
Mezger, Markus [2 ]
Besenius, Pol [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Inst Organ Chem, Duesbergweg 10-14, D-55128 Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Max Planck Inst Polymer Res, Inst Phys, Ackermannweg 10, D-55128 Mainz, Germany
关键词
dynamic materials; kinetic control; redox regulation; self-assembly; supramolecular chemistry; METHIONINE SULFOXIDE; SYSTEMS CHEMISTRY; TEMPORAL CONTROL; HYDROGELS; POLYMERS; VESICLES; DRIVEN; GEL; RESPONSIVENESS; ASSEMBLIES;
D O I
10.1002/anie.201708857
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A multistimuli-responsive transient supramolecular polymerization of beta-sheet-encoded dendritic peptide monomers in water is presented. The amphiphiles, which contain glutamic acid and methionine, undergo a glucose oxidase catalyzed, glucose-fueled transient hydrogelation in response to an interplay of pH and oxidation stimuli, promoted by the production of reactive oxygen species (ROS). Adjusting the enzyme and glucose concentration allows tuning of the assembly and the disassembly rates of the supramolecular polymers, which dictate the stiffness and transient stability of the hydrogels. The incorporation of triethylene glycol chains introduces thermoresponsive properties to the materials. We further show that repair enzymes are able to reverse the oxidative damage in the methionine-based thioether side chains. Since ROS play an important role in signal transduction cascades, our strategy offers great potential for applications of these dynamic biomaterials in redox micro-environments.
引用
收藏
页码:15461 / 15465
页数:5
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