Department of Chemistry, Johannes Gutenberg University Mainz, Duesbergweg 10-14, 55128, Mainz, Germany.
Institute for Physiological Chemistry, University Medical Center Mainz, Duesbergweg 6, 55128, Mainz, Germany.
Adv Mater. 2024 Jun;36(26):e2313270. doi: 10.1002/adma.202313270. Epub 2024 Apr 5.
Printing of biologically functional constructs is significant for applications in tissue engineering and regenerative medicine. Designing bioinks remains remarkably challenging due to the multifaceted requirements in terms of the physical, chemical, and biochemical properties of the three-dimensional matrix, such as cytocompatibility, printability, and shape fidelity. In order to promote matrix and materials stiffness, while not sacrificing stress relaxation mechanisms which support cell spreading, migration, and differentiation, this work reports an interpenetrating network (IPN) bioink design. The approach makes use of a chemically defined network, combining physical and chemical crosslinking units with a tunable composition and network density, as well as spatiotemporal control over post-assembly material stiffening. To this end, star-shaped poly(ethylene glycol)s functionalized with Phe-Gly-Gly tripeptide or photoactive stilbazolium are synthesized, and used to prepare three-dimensional networks with cucurbit[8]uril (CB[8]) through supramolecular host-guest complexation. The hydrogel obtained shows fast relaxation and thus supports the proliferation and differentiation of cells. Upon irradiation, the mechanical properties of the hydrogel can be rapidly adapted via selective photochemical dimerization of stilbazolium within CB[8], leading to IPNs with increased form stability while retaining the dynamic nature of the hydrogels. This modular approach opens new design opportunities for extrudable and cell-friendly dynamic biomaterials for applications in 3D-bioprinting.
生物功能结构的打印对于组织工程和再生医学的应用非常重要。由于三维基质在物理、化学和生物化学性质方面的多方面要求,如细胞相容性、可打印性和形状保真度,设计生物墨水仍然极具挑战性。为了促进基质和材料的硬度,同时不牺牲支持细胞扩散、迁移和分化的应力松弛机制,本工作报告了一种互穿网络(IPN)生物墨水设计。该方法利用化学定义的网络,结合物理和化学交联单元,具有可调组成和网络密度,以及对组装后材料增硬的时空控制。为此,合成了星形聚乙二醇(PEG),其功能化有苯丙氨酸-甘氨酸-甘氨酸三肽或光活性芐基芐基,通过超分子主客体络合作用与葫芦[8]脲(CB[8])制备三维网络。所得水凝胶表现出快速松弛,从而支持细胞的增殖和分化。光照后,通过 CB[8]内芐基芐基的选择性光化学二聚化,可以快速适应水凝胶的机械性能,从而得到具有增加的形态稳定性的 IPN,同时保持水凝胶的动态性质。这种模块化方法为可挤出和细胞友好的动态生物材料在 3D 生物打印中的应用开辟了新的设计机会。