儿茶酚
自愈水凝胶
胶粘剂
表面改性
粘附
生物分子
明胶
化学
高分子化学
纳米技术
材料科学
有机化学
物理化学
图层(电子)
作者
Hossein Montazerian,Subir K. Mitra,Alireza Hassani Najafabadi,Rasoul Seyedmahmoud,Yuting Zheng,Mehmet R. Dokmeci,Nasim Annabi,Ali Khademhosseini,Paul S. Weiss
标识
DOI:10.1021/acsmaterialslett.3c00193
摘要
Inspired by mussel adhesion, catechol functionalization of different biomacromolecules has become a popular technique to impart adhesion to biomaterials. However, the bioadhesion capacity of catechol motifs in hydrogels that cross-link through free-radical-based systems is debated. Here, we revisit the bioadhesion efficacy of catechol functionalization in methacryloyl-modified photo-cross-linkable biomaterials. For this purpose, gelatin biomolecules functionalized with caffeic acid (CA) and methacryloyl groups are cross-linked using UV light to assess their cross-linking and bioadhesion. Despite the typical emphasis on wet adhesion of catecholic biomaterials, samples with larger catechol content showed lower adhesion strength, particularly when bioadhesives are cross-linked in situ as injectable sealants. Cross-linking was found to decay toward the interface with the substrates as more catechol groups are introduced to the hydrogels, which further undermines hydrogel integrity and adhesive bonds. Finally, cytotoxic and immunostimulatory effects associated with the catechol groups are evaluated for their translational potential in clinical applications.
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