使用有色超分子水凝胶防止腱鞘粘连。

Emily L Meany, Christian M Williams, Ye Eun Song, Vanessa M Doulames, Sophia J Bailey, Shoshana C Williams, Carolyn K Jons, Paige M Fox, Eric A Appel
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引用次数: 0

摘要

在美国,每年因手部屈肌腱损伤而就诊的150万例急诊中,超过30-40%的患者会出现肌腱粘连,从而限制活动范围(ROM),严重影响患者的生活质量。粘连是一种纤维状疤痕样组织,可在身体相邻组织之间形成,以应对损伤、炎症或手术后的正常愈合。目前,还没有广泛的解决方案,以防止粘连的微妙空间的手指,同时允许患者术后迅速充分的ROM。明确的临床需要一种能够限制粘连形成的材料,这种材料应用简单,不影响愈合,在运动和初始炎症期间(数天-数周)保持在应用部位,并且使肌腱滑动不受阻碍。在这项工作中,我们开发了动态交联的、生物可吸收的超分子水凝胶,作为易于应用的色屏障,以防止肌腱粘连的形成。这些水凝胶具有优异的长期稳定性、可注射性和热稳定的粘弹性,易于储存和使用。我们评估了水凝胶与相关组织(包括人体肌腱和皮肤)在剪切和拉伸应力模式下的界面相互作用,并展示了一种基于维持组织之间的色系水凝胶屏障的独特粘连预防机制。离体研究表明,在临床上相关的屈肌腱修复后,将水凝胶应用于尸体人手时,不会损害肌腱的滑动行为和力学性能。我们进一步将这些水凝胶应用于临床前大鼠跟腱损伤模型,观察到修复部位的局部保留时间延长,并改善了关键功能指标的恢复,包括ROM和最大背屈。此外,与目前的护理标准相比,这些水凝胶是安全的,不会损害肌腱强度和愈合。这些动态的,生物相容性的水凝胶提出了一种新的解决方案,具有明确的翻译潜力的腹膜粘连的重大问题。
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Preventing peritendinous adhesions using lubricious supramolecular hydrogels.

Of the 1.5 million emergency room visits each year in the United States due to flexor tendon injuries in the hand, over 30-40% result in peritendinous adhesions which can limit range of motion (ROM) and severely impact an individual's quality of life. Adhesions are fibrous scar-like tissues which can form between adjacent tissues in the body in response to injury, inflammation, or during normal healing following surgery. Currently, there is no widespread solution for adhesion prevention in the delicate space of the digit while allowing a patient full ROM quickly after surgery. There is a clear clinical need for a material capable of limiting adhesion formation which is simple to apply, does not impair healing, remains at the application site during motion and initial inflammation (days - weeks), and leaves tendon glide unencumbered. In this work, we developed dynamically crosslinked, bioresorbable supramolecular hydrogels as easy-to-apply lubricious barriers to prevent the formation of peritendinous adhesions. These hydrogels exhibit excellent long-term stability, injectability, and thermally stable viscoelastic properties that allow for simple storage and facile application. We evaluated interactions at the interface of the hydrogels and relevant tissues, including human tendon and skin, in shear and extensional stress modes and demonstrated a unique mechanism of adhesion prevention based on maintenance of a lubricious hydrogel barrier between tissues. Ex vivo studies show that the hydrogels did not impair the gliding behavior nor mechanical properties of tendons when applied in cadaveric human hands following clinically relevant flexor tendon repair. We further applied these hydrogels in a preclinical rat Achilles tendon injury model and observed prolonged local retention at the repair site as well as improved recovery of key functional metrics, including ROM and maximal dorsiflexion. Further, these hydrogels were safe and did not impair tendon strength nor healing compared to the current standard of care. These dynamic, biocompatible hydrogels present a novel solution to the significant problem of peritendinous adhesions with clear translational potential.

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