Bader Rebecca A
School of Pharmacy, University of Wisconsin-Madison, Madison, WI 53705, USA.
Acta Biomater. 2008 Jul;4(4):967-75. doi: 10.1016/j.actbio.2008.02.015. Epub 2008 Mar 4.
Hydrogels have been proposed as candidates for tissue replacement; however, current systems are often highly susceptible to hydrolytic degradation and have not been shown to mimic the viscoelastic behavior of the native tissue when subjected to dynamic loading conditions. In the present work, 1,2-epoxy-5-hexene modified poly(vinyl alcohol) was crosslinked via photopolymerization to generate non-degradable hydrogels with mechanical properties and network characteristics that could be modulated through variation in the type and percentage of a monomeric additive. Complex shear moduli obtained from dynamic frequency sweeps in torsional shear were used to exemplify the differences in the viscoelastic behavior of the materials, and the corresponding changes in crosslink density were determined by rubber elasticity theory. Hydrolysis resistance was assessed by monitoring variations in the moduli of hydrogels submerged in Hank's balanced salt solution for progressively longer periods of time. Over the time-frame of the experiment, no change in the viscoelastic behavior was observed. Direct contact assays and elution tests were used to demonstrate that the system was non-cytotoxic. This study represents a successful attempt to generate a non-degradable hydrogel system with viscoelastic behavior that can be readily modulated to match that of soft biological tissues for use in tissue replacement.
水凝胶已被提议作为组织替代物的候选材料;然而,目前的体系往往极易受到水解降解的影响,并且在动态加载条件下尚未显示出能够模拟天然组织的粘弹性行为。在本研究中,1,2 - 环氧 - 5 - 己烯改性的聚乙烯醇通过光聚合进行交联,以生成具有机械性能和网络特性的不可降解水凝胶,这些性能和特性可通过改变单体添加剂的类型和百分比来调节。通过在扭转剪切中进行动态频率扫描获得的复数剪切模量用于例证材料粘弹性行为的差异,并且根据橡胶弹性理论确定交联密度的相应变化。通过监测在汉克平衡盐溶液中浸泡时间逐渐延长的水凝胶模量变化来评估耐水解性。在实验时间范围内,未观察到粘弹性行为的变化。直接接触试验和洗脱试验用于证明该体系无细胞毒性。本研究代表了一次成功的尝试,即生成一种具有粘弹性行为的不可降解水凝胶体系,该体系可轻松调节以匹配用于组织替代的软生物组织的粘弹性行为。