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首页> 外文期刊>Reactive & Functional Polymers >Preparation and fracture process of high strength hyaluronic acid hydrogels cross-linked by ethylene glycol diglycidyl ether
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Preparation and fracture process of high strength hyaluronic acid hydrogels cross-linked by ethylene glycol diglycidyl ether

机译:乙二醇二缩水甘油醚交联的高强度透明质酸水凝胶的制备及断裂工艺

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We present a synthetic strategy to produce high-strength hydrogels based on hyaluronic acid, a unique biomacromolecule with distinctive biological functions. The hydrogels were prepared using a two-step procedure. In the first step, hyaluronic acid (HA) was chemically cross-linked in aqueous solutions using ethylene glycol diglycidyl ether (EGDE) under various experimental conditions. EGDE-cross-linked HA hydrogels containing 97-99% water were fragile, and ruptured when compressed to 25-51% strain under 0.02-0.15 MPa stresses. By applying the double-network approach in the second step, we were able to generate high strength HA/poly(N,N-dimethylacrylamide) double-network hydrogels containing 84-94% water. Tuning the ratio of the network components could result in hydrogels exhibiting a compressive modulus of 0.9 MPa that sustain 19.4 MPa compressive stresses, which are much larger than those reported before for the hydrogels derived from the methacrylated HA macromers. Thus, the hydrogels presented here are promising materials to make use the characteristics of HA in stress-bearing biomedical applications. Cyclic mechanical tests show irreversible stress-strain curves with a large hysteresis indicating that elastically effective cross-links of HA first-network are irreversibly destroyed under load by dissipating energy. This internal fracture of HA network together with the high mass ratio of the second to the first-network components are responsible for the extraordinary mechanical properties of the hydrogels. (C) 2016 Elsevier B.V. All rights reserved.
机译:我们提出了一种基于透明质酸生产高强度水凝胶的合成策略,透明质酸是具有独特生物学功能的独特生物大分子。使用两步法制备水凝胶。第一步,在各种实验条件下,使用乙二醇二缩水甘油醚(EGDE)在水溶液中化学交联透明质酸(HA)。含有97-99%水的EGDE交联HA水凝胶易碎,在0.02-0.15 MPa压力下压缩至25-51%应变时会破裂。通过在第二步中应用双网络方法,我们能够生成包含84-94%水的高强度HA /聚(N,N-二甲基丙烯酰胺)双网络水凝胶。调整网络组分的比例可能会导致水凝胶显示0.9 MPa的压缩模量,可承受19.4 MPa的压缩应力,这比之前报道的衍生自甲基丙烯酸HA大分子单体的水凝胶要大得多。因此,本文介绍的水凝胶是在有压力的生物医学应用中利用HA特性的有前途的材料。循环力学测试表明,不可逆的应力-应变曲线具有较大的滞后性,表明HA第一网的弹性有效交联在负载下通过耗散能量而不可逆地破坏。 HA网络的内部断裂以及第二个与第一个网络组分的高质量比共同导致了水凝胶的非凡机械性能。 (C)2016 Elsevier B.V.保留所有权利。

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