Molecularly Engineered Supramolecular Thermoresponsive Hydrogels with Tunable Mechanical and Dynamic Properties
Laura Rijns, Heleen Duijs, René P. M. Lafleur, Ruth Cardinaels, Anja R. A. Palmans, Patricia Y. W. Dankers, Lu Su
Abstract
High Resolution Image Download MS PowerPoint Slide Synthetic supramolecular polymers and hydrogels in water are emerging as promising biomaterials due to their modularity and intrinsic dynamics. Here, we introduce temperature sensitivity into the nonfunctionalized benzene-1,3,5-tricarboxamide ( BTA-EG 4 ) supramolecular system by incorporating a poly( N -isopropylacrylamide)-functionalized ( BTA-PNIPAM) moiety, enabling 3D cell encapsulation applications. The viscous and structural properties in the solution state as well as the mechanical and dynamic features in the gel state of BTA-PNIPAM/BTA-EG 4 mixtures were investigated and modulated. In the dilute state ( c ∼μM), BTA-PNIPAM acted as a chain capper below the cloud point temperature ( T cp = 24 °C) but served as a cross-linker above T cp . At higher concentrations ( c ∼mM), weak or stiff hydrogels were obtained, depending on the BTA-PNIPAM/BTA-EG 4 ratio. The mixture with the highest BTA-PNIPAM ratio was ∼100 times stiffer and ∼10 times less dynamic than BTA-EG 4 hydrogel. Facile cell encapsulation in 3D was realized by leveraging the temperature-sensitive sol–gel transition, opening opportunities for utilizing this hydrogel as an extracellular matrix mimic.