Department of Materials Chemistry, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Japan.
Department of Energy Engineering, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Japan.
Int J Mol Sci. 2021 Apr 15;22(8):4104. doi: 10.3390/ijms22084104.
Physically crosslinked hydrogels with thixotropic properties attract considerable attention in the biomedical research field because their self-healing nature is useful in cell encapsulation, as injectable gels, and as bioinks for three-dimensional (3D) bioprinting. Here, we report the formation of thixotropic hydrogels containing nanofibers of double-hydrophobic elastin-like polypeptides (ELPs). The hydrogels are obtained with the double-hydrophobic ELPs at 0.5 wt%, the concentration of which is an order of magnitude lower than those for previously reported ELP hydrogels. Although the kinetics of hydrogel formation is slower for the double-hydrophobic ELP with a cell-binding sequence, the storage moduli G' of mature hydrogels are similar regardless of the presence of a cell-binding sequence. Reversible gel-sol transitions are demonstrated in step-strain rheological measurements. The degree of recovery of the storage modulus G' after the removal of high shear stress is improved by chemical crosslinking of nanofibers when intermolecular crosslinking is successful. This work would provide deeper insight into the structure-property relationships of the self-assembling polypeptides and a better design strategy for hydrogels with desired viscoelastic properties.
具有触变性的物理交联水凝胶在生物医学研究领域引起了相当大的关注,因为其自修复特性在细胞包封、可注射凝胶和用于三维(3D)生物打印的生物墨水方面非常有用。在这里,我们报告了含有双疏弹性蛋白样多肽(ELP)纳米纤维的触变水凝胶的形成。水凝胶是通过浓度为 0.5wt%的双疏 ELPs 获得的,其浓度比以前报道的 ELP 水凝胶低一个数量级。尽管具有细胞结合序列的双疏 ELP 的水凝胶形成动力学较慢,但无论是否存在细胞结合序列,成熟水凝胶的储能模量 G'都相似。在分步应变流变学测量中证明了可逆的凝胶-溶胶转变。当分子间交联成功时,通过纳米纤维的化学交联可以提高在高剪切应力去除后储能模量 G'的恢复程度。这项工作将深入了解自组装多肽的结构-性能关系,并为具有所需粘弹性的水凝胶提供更好的设计策略。