自愈水凝胶
明胶
细胞包封
材料科学
超分子化学
纳米技术
动力学
真皮成纤维细胞
生物物理学
药物输送
细胞外基质
化学工程
成纤维细胞
化学
高分子化学
有机化学
分子
体外
生物化学
生物
物理
量子力学
工程类
作者
Amy C. Madl,Christopher M. Madl,David Myung
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2020-04-08
卷期号:9 (4): 619-626
被引量:43
标识
DOI:10.1021/acsmacrolett.0c00184
摘要
Recent efforts to develop hydrogel biomaterials have focused on better recapitulating the dynamic properties of the native extracellular matrix. In hydrogel biomaterials, binding thermodynamics and cross-link kinetics directly affect numerous bulk dynamic properties such as strength, stress relaxation, and material clearance. However, despite the broad range of bulk dynamic properties observed in biological tissues, present strategies to incorporate dynamic linkages in cell-encapsulating hydrogels rely on a relatively small number of dynamic covalent chemical reactions and host-guest interactions. To expand this toolkit, we report the preparation of supramolecular gelatin hydrogels with cucurbit[8]uril (CB[8])-based cross-links that form on demand via thiol-ene reactions between preassembled CB[8]·FGGC peptide ternary complexes and grafted norbornenes. Human fibroblast cells encapsulated within these optically transparent, shear thinning, injectable hydrogels remained highly viable and exhibited a well-spread morphology in culture. These CB[8]-based gelatin hydrogels are anticipated to be useful in applications ranging from bioprinting to cell and drug delivery.
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