John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, 02138, USA.
Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, 02115, USA.
Adv Mater. 2022 Sep;34(35):e2205567. doi: 10.1002/adma.202205567. Epub 2022 Jul 28.
Tissue adhesives capable of achieving strong and tough adhesion in permeable wet environments are useful in many biomedical applications. However, adhesion generated through covalent bond formation directly with the functional groups of tissues (i.e., COOH and NH groups in collagen), or using non-covalent interactions can both be limited by weak, unstable, or slow adhesion. Here, it is shown that by combining pH-responsive bridging chitosan polymer chains and a tough hydrogel dissipative matrix one can achieve unprecedented ultratough adhesion to tissues (>2000 J m ) in 5-10 min without covalent bond formation. The strong non-covalent adhesion is shown to be stable under physiologically relevant conditions and strongly influenced by chitosan molecular weight, molecular weight of polymers in the matrix, and pH. The adhesion mechanism relies primarily on the topological entanglement between the chitosan chains and the permeable adherends. To further expand the applicability of the adhesives, adhesion time can be decreased by dehydrating the hydrogel matrix to facilitate rapid chitosan interpenetration and entanglement (>1000 J m in ≤1 min). The unprecedented adhesive properties presented in this study open opportunities for new strategies in the development of non-covalent tissue adhesives and numerous bioapplications.
能够在可渗透的湿环境中实现强韧黏附的组织胶粘剂在许多生物医学应用中非常有用。然而,通过与组织的官能团(即胶原蛋白中的COOH 和 NH 基团)直接形成共价键,或利用非共价相互作用产生的黏附,都可能受到弱、不稳定或缓慢的黏附的限制。在这里,通过结合 pH 响应性桥接壳聚糖聚合物链和坚韧的水凝胶耗散基质,可以实现在 5-10 分钟内无需形成共价键即可实现对组织的前所未有的超强黏附(>2000 J m )。研究表明,这种强非共价黏附在生理相关条件下稳定,并强烈受壳聚糖分子量、基质中聚合物的分子量和 pH 值的影响。黏附机制主要依赖于壳聚糖链与可渗透的黏附物之间的拓扑缠结。为了进一步扩大胶粘剂的适用性,可以通过使水凝胶基质脱水来缩短黏附时间,以促进壳聚糖的快速渗透和缠结(>1000 J m ,在≤1 分钟内)。本研究中呈现的前所未有的黏附性能为非共价组织胶粘剂的开发和许多生物应用提供了新的策略机会。