Department of Chemistry, College of Natural Sciences, Colorado State University, Fort Collins, CO, USA.
Organogenesis. 2011 Jan-Mar;7(1):42-9. doi: 10.4161/org.7.1.14029. Epub 2011 Jan 1.
As the world of critical care medicine advances, extracorporeal therapies (ECC) have become commonplace in the management of the high risk intensive care patient. ECC encompasses a wide variety of technologies from hemodialysis, continuous renal replacement therapy (CRRT) and plasmapheresis, to cardiopulmonary bypass (CPB), extracorporeal life support (ECLS) and hepatic support. The development of internal man made organs is the next step with ventricular assist devices and artificial lungs. As we advance the technologies with smaller devices, and more intricate circuitry, we lack the keystone necessary to control the blood-biomaterial interface. For the last 50 years much has been learned about surface induced thrombosis and attempts have been made to prevent it with alternative systemic anticoagulation, circuitry surface modifications, or a combination of both. Despite these efforts, systemic or regional anticoagulation remain necessary for both laboratory and clinical application of ECC. As such, the development of an endothelial-like, biomimetic surface to reduce or perhaps even eliminate the blood activation/thrombus formation events that occur upon exposure to artificial surfaces is paramount.
随着危重病医学领域的发展,体外治疗(ECC)已成为高危重症监护患者治疗的常规手段。ECC 涵盖了从血液透析、连续肾脏替代疗法(CRRT)和血浆置换到体外心肺旁路(CPB)、体外生命支持(ECLS)和肝脏支持等多种技术。下一步是开发内部人造器官,包括心室辅助装置和人工肺。随着我们使用更小的设备和更复杂的电路来推进技术,我们缺乏控制血液-生物材料界面的关键因素。在过去的 50 年中,人们已经了解了表面诱导的血栓形成,并尝试通过替代全身抗凝、电路表面改性或两者结合来预防它。尽管做出了这些努力,但 ECC 的实验室和临床应用仍需要全身或局部抗凝。因此,开发一种类似于内皮的仿生表面来减少甚至消除人工表面暴露时发生的血液激活/血栓形成事件至关重要。