Molecularly Engineered Supramolecular Thermoresponsive Hydrogels with Tunable Mechanical and Dynamic Properties

被引:3
|
作者
Rijns, Laura [1 ]
Duijs, Heleen [2 ]
Lafleur, Rene P. M. [3 ]
Cardinaels, Ruth [4 ,5 ]
Palmans, Anja R. A. [3 ]
Dankers, Patricia Y. W. [1 ]
Su, Lu [2 ]
机构
[1] Eindhoven Univ Technol, Inst Complex Mol Syst ICMS, Dept Biomed Engn, NL-5600 MB Eindhoven, Netherlands
[2] Leiden Univ, Leiden Acad Ctr Drug Res LACDR, NL-2333 AL Leiden, Netherlands
[3] Eindhoven Univ Technol, Inst Complex Mol Syst ICMS, Dept Chem Engn & Chem, Lab Macromol & Organ Chem, NL-5600 MB Eindhoven, Netherlands
[4] Eindhoven Univ Technol, Inst Complex Mol Syst ICMS, Dept Mech Engn, Proc & Performance Mat, NL-5600 MB Eindhoven, Netherlands
[5] Katholieke Univ Leuven, Dept Chem Engn, Soft Matter Rheol & Technol, B-3001 Leuven, Belgium
基金
欧洲研究理事会; 荷兰研究理事会;
关键词
EXTRACELLULAR-MATRIX; PNIPAM; VISCOELASTICITY; SCAFFOLDS; STIFFNESS; POLYMERS; RECOVERY;
D O I
10.1021/acs.biomac.3c01357
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 similar to mu M), BTA-PNIPAM acted as a chain capper below the cloud point temperature (T-cp = 24 degrees C) but served as a cross-linker above T-cp. At higher concentrations (c similar to 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 similar to 100 times stiffer and similar to 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.
引用
收藏
页码:4686 / 4696
页数:11
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