Department of Mechanical Engineering, École de Technologie Supérieure, Montreal, Quebec, Canada H3C1K3.
J Biomed Mater Res B Appl Biomater. 2013 Jan;101(1):153-61. doi: 10.1002/jbm.b.32828. Epub 2012 Oct 22.
A new injectable radiopaque embolizing agent has been developed, based on chitosan thermogelling properties. Different commercial contrast agents (Isovue®, Visipaque®, and Conray®) were associated with chitosan-β-glycerophosphate. Their impact on gelation kinetic, mechanical properties, radiopacity, and cytotoxicity was tested to evaluate the best candidate and its feasibility for the treatment of endoleaks after endovascular aneurysm repair (EVAR). Addition of contrast agents did not prevent gelation at body temperature, but it significantly increased the viscosity of the solution before gelation, delayed gelation, and reduced the gelation rate. However, using chitosan with a high degree of deacetylation and 20 vol % contrast agent made it possible to obtain a gel with rapid gelation that was visible during X-ray based guided intervention. Hydrogels exhibit relatively low mechanical properties, which are only slightly modified by the addition of contrast agents. In vitro studies have demonstrated rapid release of contrast agents from hydrogels when immersed in a saline solution (>50% within 4 h). This is suitable for embolization, as radiopacity is required only to follow the embolization procedure, while long-term radiopacity would hamper further imaging and endoleak detection. Cytotoxicity and osmolality testing of extracts demonstrated some toxicity of products released by the gel during the first few hours, which is mainly related to their hypertonicity. After the first 24 h incubation, hydrogels released no more cytotoxic compounds, suggesting that the hydrogel rapidly becomes biocompatible. Altogether, this study suggests that the new radiopaque thermogels present interesting characteristics as embolizing agents for EVAR, although their mechanical properties require improvement.
一种新型的可注射的、基于壳聚糖温敏凝胶特性的放射显影栓塞剂已经被开发出来。不同的商业对比剂(Isovue®、Visipaque®和Conray®)与壳聚糖-β-甘油磷酸酯相关联。研究了它们对凝胶动力学、力学性能、放射显影性和细胞毒性的影响,以评估最佳候选物及其在血管内动脉瘤修复(EVAR)后治疗内漏的可行性。添加对比剂并不能阻止在体温下凝胶化,但它显著增加了凝胶化前溶液的粘度,延迟了凝胶化过程,并降低了凝胶化速率。然而,使用高脱乙酰度的壳聚糖和 20%体积的对比剂,使得可以获得一种快速凝胶化的凝胶,这种凝胶在 X 射线引导的介入过程中是可见的。水凝胶表现出相对较低的机械性能,而添加对比剂仅略微改变了这些性能。体外研究表明,当水凝胶浸泡在盐溶液中时,对比剂会迅速从水凝胶中释放出来(4 小时内超过 50%)。这对于栓塞是合适的,因为放射显影仅用于跟踪栓塞过程,而长期的放射显影会妨碍进一步的成像和内漏检测。提取物的细胞毒性和渗透压测试表明,凝胶在最初几个小时内释放的产物具有一定的毒性,这主要与其高渗性有关。在最初的 24 小时孵育后,水凝胶不再释放更多的细胞毒性化合物,这表明水凝胶迅速变得具有生物相容性。总之,这项研究表明,新型放射显影温敏凝胶作为 EVAR 的栓塞剂具有有趣的特性,尽管它们的机械性能需要改进。