生物粘附
凝聚
粘附
甲基丙烯酸酯
普鲁兰
单宁酸
胶粘剂
聚合物
氰基丙烯酸酯
材料科学
高分子科学
组织粘连
高分子化学
光致聚合物
化学工程
甲基丙烯酸
化学
聚丙烯酸
生物污染
伤口愈合
湿强度
离子强度
伤口闭合
纳米技术
表面改性
羧甲基纤维素钠
复合材料
作者
Margarida M. A. Sacramento,Mariana B. Oliveira,José R. B. Gomes,João Borges,Benjamin R. Freedman,David Mooney,João M. M. Rodrigues,João F. Mano
标识
DOI:10.1002/adhm.202304587
摘要
Abstract Medical adhesives are emerging as an important clinical tool as adjuvants for sutures and staples in wound closure and healing and in the achievement of hemostasis. However, clinical adhesives combining cytocompatibility, as well as strong and stable adhesion in physiological conditions, are still in demand. Herein, a mussel‐inspired strategy is explored to produce adhesive coacervates using tannic acid (TA) and methacrylate pullulan (PUL‐MA). TA | PUL‐MA coacervates mainly comprise van der Waals forces and hydrophobic interactions. The methacrylic groups in the PUL backbone increase the number of interactions in the adhesives matrix, resulting in enhanced cohesion and adhesion strength (72.7 Jm −2 ), compared to the non‐methacrylated coacervate. The adhesive properties are kept in physiologic‐mimetic solutions (72.8 Jm −2 ) for 72 h. The photopolymerization of TA | PUL‐MA enables the on‐demand detachment of the adhesive. The poor cytocompatibility associated with the use of phenolic groups is here circumvented by mixing reactive oxygen species‐degrading enzyme in the adhesive coacervate. This addition does not hamper the adhesive character of the materials, nor their anti‐microbial or hemostatic properties. This affordable and straightforward methodology, together with the tailorable adhesivity even in wet environments, high cytocompatibility, and anti‐bacterial activity, enables foresee TA | PUL‐MA as a promising ready‐to‐use bioadhesive for biomedical applications.
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