Zhang Bin, Qiu Jianhui, Meng Xuefen, Sakai Eiichi, Feng Huixia, Zhang Liang, Tang Jianhua, Zhang Guohong, Wu Hong, Guo Shaoyun
Department of Mechanical Engineering, Faculty of Systems Science and Technology, Akita Prefectural University, Akita 015-0055, Japan.
College of Petrochemical Technology, Lanzhou University of Technology, Lanzhou 730050, China.
ACS Appl Mater Interfaces. 2024 Oct 23;16(42):57769-57777. doi: 10.1021/acsami.4c14884. Epub 2024 Oct 9.
The biocompatibility and adaptability of hydrogels make them ideal candidates for use as artificial tendons and muscles in clinical applications, where both muscle-like strength and low hysteresis are essential. However, achieving a balance between a high strength and low hysteresis in hydrogels remains a significant challenge. Herein, we demonstrated a self-assembly process of heterogeneous hydrogels to meet the dilemma. And the hydrogels are composed of both hydrophilic and hydrophobic polymers. The hydrophilic network absorbs water, causing phase separation into a water-rich phase and a water-poor phase, while hydrophobic polymers and entanglement of the network arrest phase separation. Our results demonstrated that these hydrogels achieve remarkable mechanical properties, with a strength of 848.8 kPa, a low energy loss of 19.6 kJ/m, and minimal hysteresis (0.046) during loading-unloading cycles. The reinforcing mechanisms underlying these properties are attributed to crystallization, molecular entanglement, and chain rearrangement induced by stretching. Furthermore, the combination of hydrophilic and hydrophobic networks is exceedingly rare in reported hydrogels.
水凝胶的生物相容性和适应性使其成为临床应用中用作人工肌腱和肌肉的理想候选材料,在临床应用中,类似肌肉的强度和低滞后性都是必不可少的。然而,在水凝胶中实现高强度和低滞后性之间的平衡仍然是一个重大挑战。在此,我们展示了一种非均相水凝胶的自组装过程,以应对这一困境。这些水凝胶由亲水和疏水聚合物组成。亲水网络吸收水分,导致相分离成富水相和贫水相,而疏水聚合物和网络缠结阻止了相分离。我们的结果表明,这些水凝胶具有卓越的机械性能,强度为848.8 kPa,能量损失低至19.6 kJ/m,在加载-卸载循环中的滞后极小(0.046)。这些性能背后的增强机制归因于结晶、分子缠结以及拉伸诱导的链重排。此外,亲水和疏水网络的结合在已报道的水凝胶中极为罕见。