Polymer Science and Engineering Department, University of Massachusetts Amherst, 120 Governors Drive, Amherst, Massachusetts 01003, USA.
Soft Matter. 2018 May 9;14(18):3478-3489. doi: 10.1039/c8sm00501j.
Detailed understanding of the local structure-property relationships in soft biopolymeric hydrogels can be instrumental for applications in regenerative tissue engineering. Resilin-like polypeptide (RLP) hydrogels have been previously demonstrated as useful biomaterials with a unique combination of low elastic moduli, excellent resilience, and cell-adhesive properties. However, comprehensive mechanical characterization of RLP hydrogels under both low-strain and high-strain conditions has not yet been conducted, despite the unique information such measurements can provide about the local structure and macromolecular behavior underpinning mechanical properties. In this study, mechanical properties (elastic modulus, resilience, and fracture initiation toughness) of equilibrium swollen resilin-based hydrogels were characterized via oscillatory shear rheology, small-strain microindentation, and large-strain puncture tests as a function of polypeptide concentration. These methods allowed characterization, for the first time, of the resilience and failure in hydrogels with low polypeptide concentrations (<20 wt%), as the employed methods obviate the handling difficulties inherent in the characterization of such soft materials via standard mechanical techniques, allowing characterization without any special sample preparation and requiring minimal volumes (as low as 50 μL). Elastic moduli measured from small-strain microindentation showed good correlation with elastic storage moduli obtained from oscillatory shear rheology at a comparable applied strain rate, and evaluation of multiple loading-unloading cycles revealed decreased resilience values at lower hydrogel concentrations. In addition, large-strain indentation-to-failure (or puncture) tests were performed to measure large-strain mechanical response and fracture toughness on length scales similar to biological cells (∼10-50 μm) at various polypeptide concentrations, indicating very high fracture initiation toughness for high-concentration hydrogels. Our results establish the utility of employing microscale mechanical methods for the characterization of the local mechanical properties of biopolymeric hydrogels of low concentrations (<20 wt%), and show how the combination of small and large-strain measurements can provide unique insight into structure-property relationships for biopolymeric elastomers. Overall, this study provides new insight into the effects on local mechanical properties of polypeptide concentration near the overlap polymer concentration c* for resilin-based hydrogels, confirming their unique elastomeric features for applications in regenerative medicine.
详细了解软生物聚合物水凝胶中的局部结构-性能关系对于再生组织工程中的应用非常重要。类弹性蛋白多肽(RLP)水凝胶已被证明是一种有用的生物材料,具有低弹性模量、优异的弹性和细胞粘附特性的独特组合。然而,尽管这种测量方法可以提供有关机械性能基础的局部结构和大分子行为的独特信息,但尚未对 RLP 水凝胶在低应变和高应变条件下进行全面的力学特性表征。在这项研究中,通过振荡剪切流变学、小应变微压痕和大应变穿刺测试,研究了平衡溶胀的类弹性蛋白基水凝胶的力学性能(弹性模量、弹性和起始断裂韧性),作为多肽浓度的函数。这些方法首次允许对低多肽浓度(<20wt%)下水凝胶的弹性和失效进行表征,因为所采用的方法避免了通过标准力学技术对这种软材料进行表征所固有的处理困难,允许在无需任何特殊样品制备的情况下进行表征,并且所需的体积最小(低至 50μL)。从小应变微压痕测量得到的弹性模量与在可比的施加应变率下通过振荡剪切流变学获得的弹性储能模量具有很好的相关性,并且对多个加载-卸载循环的评估表明,在较低的水凝胶浓度下,弹性值降低。此外,还进行了大应变压痕-失效(或穿刺)测试,以在各种多肽浓度下测量类似生物细胞(~10-50μm)的长度尺度上的大应变力学响应和断裂韧性,表明高浓度水凝胶具有非常高的断裂起始韧性。我们的结果确立了采用微尺度力学方法来表征低浓度(<20wt%)生物聚合物水凝胶的局部力学性能的实用性,并展示了小应变和大应变测量的组合如何为生物聚合物弹性体提供结构-性能关系的独特见解。总的来说,这项研究为基于类弹性蛋白的水凝胶在接近聚合物浓度重叠 c*的多肽浓度下对局部力学性能的影响提供了新的认识,证实了它们在再生医学中的独特弹性特征。