Viscoelastic Silk Fibroin Hydrogels with Tunable Strength

丝素 自愈水凝胶 粘弹性 材料科学 丝绸 生物相容性 应力松弛 复合材料 动态力学分析 组织工程 化学工程 高分子化学 聚合物 生物医学工程 蠕动 冶金 工程类 医学
作者
Danyu Yao,Meiqi Li,Ting Wang,Fangfang Sun,Chang Su,Tingchun Shi
出处
期刊:ACS Biomaterials Science & Engineering [American Chemical Society]
卷期号:7 (2): 636-647 被引量:48
标识
DOI:10.1021/acsbiomaterials.0c01348
摘要

Hydrogels are often used as synthetic extracellular matrices (ECMs) for biomedical applications. Natural ECMs are viscoelastic and exhibit partial stress relaxation. However, commonly used hydrogels are typically elastic. Hydrogels developed from ECM-based proteins are viscoelastic, but they often have weak mechanical properties. Here, biocompatible viscoelastic hydrogels with excellent mechanical performance are fabricated by an all aqueous process at body or room temperature. These hydrogels offer obvious stress relaxation and tunable mechanical properties and gelation kinetics. Their compressive modulus can be controlled between 2 kPa and 1.2 MPa, covering a significant portion of the properties of native tissues. Investigation of the gelation mechanism revealed that silk fibroin gelation is caused by the synergistic effects of hydrophobic interaction and hydrogen bonding between silk fibroin molecules. Newly formed crystals serve as the cross-link sites and form a network endowing the hydrogel with stable structure, and the flexible noncrystalline silk nanofibers connect disparate silk fibroin crystals, endowing hydrogels with viscoelastic properties. The all aqueous gelation process avoids complex chemical and physical treatments and is beneficial for encapsulating cells or biomolecules. Encapsulation of chondrocytes results in high initial survival rate (95% ± 1%). These silk fibroin-based viscoelastic hydrogels, combined with superior biocompatible and tunable mechanical properties, represent an exciting option for tissue engineering and regenerative medicine.
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