Injectable Cucurbit[8]uril-Based Supramolecular Gelatin Hydrogels for Cell Encapsulation

被引:38
作者
Madl, Amy C. [1 ]
Madl, Christopher M. [4 ]
Myung, David [1 ,2 ,3 ]
机构
[1] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Byers Eye Inst, Palo Alto, CA 94303 USA
[3] VA Palo Alto Hlth Care Sys, Palo Alto, CA 94304 USA
[4] Stanford Univ, Dept Microbiol & Immunol, Baxter Lab Stem Cell Biol, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
DOUBLE-NETWORK HYDROGELS; HOST-GUEST INTERACTIONS; AMINO-ACID-COMPOSITION; BETA-CYCLODEXTRIN; RECOGNITION; COMPLEXES; CULTURE;
D O I
10.1021/acsmacrolett.0c00184
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
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 cellencapsulating 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]center dot 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.
引用
收藏
页码:619 / 626
页数:8
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