Levin Michal, Tang Yongkui, Eisenbach Claus D, Valentine Megan T, Cohen Noy
Department of Materials Science and Engineering, Technion - Israel Institute of Technology, Haifa 3200003, Israel.
Department of Mechanical Engineering, University of California, Santa Barbara, California 93106, United States.
Macromolecules. 2024 Jul 17;57(15):7074-7086. doi: 10.1021/acs.macromol.3c02635. eCollection 2024 Aug 13.
Thanks to many promising properties, including biocompatibility and the ability to experience large deformations, poly(ethylene glycol) diacrylate (PEGDA) hydrogels are excellent candidate materials for a wide range of applications. Interestingly, the polymerization of PEGDA leads to a network microstructure that is fundamentally different from that of the "classic" polymeric gels. Specifically, PEGDA hydrogels comprise PEG chains that are interconnected by multifunctional densely grafted rod-like polyacrylates (PAs), which serve as cross-linkers. In this work, we derive a microstructurally motivated model that captures the essential features which enable deformation in PEGDA hydrogels: (1) entropic elasticity of PEG chains, (2) deformation of PA rods, and (3) PA-PA interactions. Expressions for the energy-density functions and the stress associated with each of the three contributions are derived. The model demonstrates the microstructural evolution of the network during loading and reveals the role of key microscopic quantities. To validate the model, we fabricate and compress PEGDA hydrogel discs. The model is in excellent agreement with our experimental findings for a broad range of PEGDA compositions. Interestingly, we show that the response of PEGDA hydrogels with short PEG chains and long PA rods is governed by PA-PA interactions, whereas networks with longer PEG chains are dominated by entropy. To enable design, we employ the model to investigate the influence of key microstructural quantities, such as the length of the PEG and the PA chains, on the macroscopic properties and response. The findings from this work pave the way to the efficient design of PEGDA hydrogels with tunable properties and behaviors, which will enable the optimization of their performance in various applications.
由于具有许多优良特性,包括生物相容性和能够经历大变形,聚乙二醇二丙烯酸酯(PEGDA)水凝胶是广泛应用的优秀候选材料。有趣的是,PEGDA的聚合导致一种网络微观结构,它与“经典”聚合物凝胶的微观结构有根本不同。具体而言,PEGDA水凝胶由通过多功能密集接枝的棒状聚丙烯酸酯(PA)相互连接的PEG链组成,PA充当交联剂。在这项工作中,我们推导了一个基于微观结构的模型,该模型捕捉了使PEGDA水凝胶能够变形的基本特征:(1)PEG链的熵弹性,(2)PA棒的变形,以及(3)PA - PA相互作用。推导了与这三种贡献中的每一种相关的能量密度函数和应力的表达式。该模型展示了加载过程中网络的微观结构演变,并揭示了关键微观量的作用。为了验证该模型,我们制备并压缩了PEGDA水凝胶圆盘。对于广泛的PEGDA组成,该模型与我们的实验结果非常吻合。有趣的是,我们表明,具有短PEG链和长PA棒的PEGDA水凝胶的响应受PA - PA相互作用控制,而具有较长PEG链的网络则由熵主导。为了实现设计,我们使用该模型来研究关键微观结构量,如PEG和PA链的长度,对宏观性质和响应的影响。这项工作的结果为高效设计具有可调特性和行为的PEGDA水凝胶铺平了道路,这将能够优化它们在各种应用中的性能。