Brisbois Elizabeth J, Major Terry C, Goudie Marcus J, Bartlett Robert H, Meyerhoff Mark E, Handa Hitesh
Department of Surgery, University of Michigan, Ann Arbor, MI, USA.
Department of Biological Engineering, University of Georgia, Athens, GA, USA.
Acta Biomater. 2016 Jun;37:111-9. doi: 10.1016/j.actbio.2016.04.025. Epub 2016 Apr 16.
Blood-contacting devices, including extracorporeal circulation (ECC) circuits, can suffer from complications due to platelet activation and thrombus formation. Development of nitric oxide (NO) releasing polymers is one method to improve hemocompatibility, taking advantage of the ability of low levels of NO to prevent platelet activation/adhesion. In this study a novel solvent swelling method is used to load the walls of silicone rubber tubing with the NO donor S-nitroso-N-acetylpenicillamine (SNAP). This SNAP-silicone rubber tubing exhibits an NO flux of ca. 1×10(-10)molcm(-2)min(-1), which mimics the range of NO release from the normal endothelium, which is stable for at least 4h. Images of the tubing before and after swelling, obtained via scanning electron microscopy, demonstrate that this swelling method has little effect on the surface properties of the tubing. The SNAP-loaded silicone rubber and silicone rubber control tubing are used to fabricate ECC circuits that are evaluated in a rabbit model of thrombogenicity. After 4h of blood flow, the SNAP-loaded silicone rubber circuits were able to preserve the blood platelet count at 64% of baseline (vs. 12% for silicone rubber control). A 67% reduction in the degree of thrombus formation within the thrombogenicity chamber was also observed. This study demonstrates the ability to improve the hemocompatibility of existing/commercial silicone rubber tubing via a simple solvent swelling-impregnation technique, which may also be applicable to other silicone-based blood-contacting devices.
Localized nitric oxide (NO) release can be achieved from biomedical grade polymers doped with S-nitroso-N-acetylpenicillamine (SNAP). Despite the promising in vitro and in vivo biocompatibility results reported for these NO releasing polymers, many of these materials may face challenges in being translated to clinical applications, especially in the areas of polymer processing and manufacturing. In this study, we report a solvent swelling-impregnation technique to incorporate SNAP into extracorporeal circuit (ECC) tubing. These NO-releasing ECCs were able to attenuate the activation of platelets and maintain their functionality, while significantly reducing the extent of thrombus formation during 4h blood flow in the rabbit model of thrombogenicity.
包括体外循环(ECC)回路在内的血液接触装置,可能会因血小板活化和血栓形成而出现并发症。开发释放一氧化氮(NO)的聚合物是提高血液相容性的一种方法,利用低水平NO防止血小板活化/黏附的能力。在本研究中,采用一种新型溶剂溶胀法将NO供体S-亚硝基-N-乙酰青霉胺(SNAP)加载到硅橡胶管管壁中。这种载有SNAP的硅橡胶管表现出约1×10⁻¹⁰mol·cm⁻²·min⁻¹的NO通量,这模拟了正常内皮细胞释放NO的范围,且至少稳定4小时。通过扫描电子显微镜获得的溶胀前后管材的图像表明,这种溶胀方法对管材的表面性能影响很小。载有SNAP的硅橡胶管和硅橡胶对照管用于制作ECC回路,并在兔血栓形成模型中进行评估。血流4小时后,载有SNAP的硅橡胶回路能够将血小板计数维持在基线的64%(而硅橡胶对照管为12%)。在血栓形成腔室内,血栓形成程度也降低了67%。本研究证明了通过一种简单的溶剂溶胀-浸渍技术提高现有/商用硅橡胶管血液相容性的能力,该技术也可能适用于其他基于硅橡胶且与血液接触的装置。
掺杂S-亚硝基-N-乙酰青霉胺(SNAP)的生物医学级聚合物能够实现局部一氧化氮(NO)释放。尽管这些释放NO的聚合物在体外和体内生物相容性方面的结果很有前景,但其中许多材料在转化为临床应用时可能面临挑战,尤其是在聚合物加工和制造领域。在本研究中,我们报告了一种溶剂溶胀-浸渍技术,将SNAP纳入体外循环(ECC)管中。这些释放NO的ECC能够减弱血小板的活化并维持其功能,同时在兔血栓形成模型中血流4小时期间显著降低血栓形成程度。