自愈水凝胶
聚合
材料科学
聚合物
明胶
生物相容性
肿胀 的
乙二醇
药物输送
丙烯酰胺
生物物理学
高分子化学
纳米技术
化学
共聚物
有机化学
复合材料
冶金
生物
作者
Ruohong Shi,Joshua Fern,Weinan Xu,Sisi Jia,Qi Huang,Gayatri Pahapale,Rebecca Schulman,David H. Gracias
出处
期刊:Small
[Wiley]
日期:2020-08-09
卷期号:16 (37): 2002946-2002946
被引量:8
标识
DOI:10.1002/smll.202002946
摘要
Hydrogels with the ability to change shape in response to biochemical stimuli are important for biosensing, smart medicine, drug delivery, and soft robotics. Here, a family of multicomponent DNA polymerization motor gels with different polymer backbones is created, including acrylamide-co-bis-acrylamide (Am-BIS), poly(ethylene glycol) diacrylate (PEGDA), and gelatin-methacryloyl (GelMA) that swell extensively in response to specific DNA sequences. A common mechanism, a polymerization motor that induces swelling is driven by a cascade of DNA hairpin insertions into hydrogel crosslinks. These multicomponent hydrogels can be photopatterned into distinct shapes, have a broad range of mechanical properties, including tunable shear moduli between 297 and 3888 Pa and enhanced biocompatibility. Human cells adhere to the GelMA-DNA gels and remain viable during ≈70% volumetric swelling of the gel scaffold induced by DNA sequences. The results demonstrate the generality of sequential DNA hairpin insertion as a mechanism for inducing shape change in multicomponent hydrogels, suggesting widespread applicability of polymerization motor gels in biomaterials science and engineering.
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