Soft Matter Sciences and Engineering, ESPCI Paris, PSL University, Sorbonne University, CNRS, F-75005, Paris, France.
Macromol Rapid Commun. 2020 Apr;41(7):e1900653. doi: 10.1002/marc.201900653. Epub 2020 Feb 18.
A novel bioinspired underwater adhesive based on the injectable aqueous solution of a graft copolymer with a thermoresponsive backbone is reported, which turns into a sticky hydrogel just below body temperature. With this topology, the collapse of the backbones upon the thermal transition leads to the formation of a percolating network of strong hydrophobic domains. Similar to pressure-sensitive adhesives (PSAs), the hydrogel goes through fibrillation and extensive energy dissipation in large deformations, giving it an edge over conventional chemical hydrogels, which are typically elastic and inherently nonsticky. This capability comes from the hydrophobic nanoscaffold, which resists large deformations to minimize its contact with water. Since hydrophobic interactions are not weakened in water, the behavior of the hydrogel is maintained in aqueous medium. Chemistry-insensitive adhesion of this hydrogel offers a major advantage over current injectable adhesives, which rely on in situ chemical crosslinking reactions with tissues.
一种基于具有温敏主链的可注射接枝共聚物的新型仿生水下胶粘剂被报道,其在体温以下会变成粘性水凝胶。通过这种拓扑结构,热转变导致的主链坍塌会形成强疏水域的渗透网络。类似于压敏胶粘剂(PSA),水凝胶在大变形下经历纤维化和广泛的能量耗散,使其优于传统的化学水凝胶,后者通常具有弹性且固有粘性。这种特性来自于疏水纳米支架,它抵抗大变形以最小化与水的接触。由于疏水相互作用在水中不会减弱,因此水凝胶的行为在水介质中得以保持。与当前依赖于与组织的原位化学交联反应的可注射胶粘剂相比,这种水凝胶的化学不敏感粘附具有很大的优势。