同步辐射成像对血液透析膜形态及人血清蛋白沉积的研究

A. Abdelrasoul
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摘要

终末期肾病(ESRD)影响着世界上约10%的人口。血液透析(HD)是ESRD或肾衰竭患者维持生命的体外血液净化方法。这种基于膜的治疗与急性副作用、危及生命的慢性疾病以及不可接受的高发病率和死亡率相关。由于HD膜的聚合物表面缺乏内皮功能,它们与人血清蛋白的相互作用会诱发炎症反应,并导致许多长期的临床后果,这些后果部分取决于膜的生物相容性程度[1]。血膜相互作用除了激活白细胞、血小板和红细胞(rbc)或通过激活补体系统或凝血因子的途径间接激活它们外,还会触发一系列多方面的蛋白质吸附事件[2,3]。因此,蛋白质吸附引起一系列生化反应,可导致HD患者出现严重的长期和短期副作用[4]。此外,人血清蛋白在膜表面的附着会显著降低尿毒症毒素的清除效率,特别是蛋白质结合的尿毒症毒素和中间分子。膜的化学组成、亲水性、表面粗糙度、孔径大小、结合亲和力等特性影响人血清蛋白与HD膜的相互作用和附着,从而影响HD患者的炎症反应。本研究突出了加拿大医院常见HD膜形态及其对人血清蛋白附着的亲和力的创新研究。加拿大光源(CLS)生物医学成像和治疗(BMIT)光束线提供的基于同步加速器的x射线成像技术已经回答了HD膜的层层形态和人血清蛋白在膜通道中的运输的关键问题。本研究将通过定性和定量分析强调同步加速器成像技术对膜表征和蛋白质沉积评估的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation on Hemodialysis Membranes Morphology and Human Serum Proteins Depositions Using Synchrotron-based Imaging
Extended Abstract End stage renal disease (ESRD) affects ~10% of the world’s population. Hemodialysis (HD) is a life-sustaining extracorporeal blood purifying method for patients with ESRD or kidney failure. This membrane-based therapy is associated with acute side effects, life-threatening chronic conditions, and unacceptably high morbidity and mortality rates. Due to the lack of endothelium functionality of the polymeric surfaces of HD membranes, their interaction with human serum proteins induces an inflammatory response and leads to numerous long-term clinical consequences that are in part determined by the degree of membrane biocompatibility[1]. Blood–membrane interactions trigger a multifaceted series of events of protein adsorption, in addition to the activation blood cells such as leukocytes, platelets, and red blood cells (RBCs) or indirectly activate them through a pathway that activates the complement system or coagulation factors [2,3]. Therefore, protein adsorption provokes a series of biochemical reactions that can lead to serious longand short-term side effects in HD patients [4]. In addition, the attachment of human serum proteins on membrane surface would significantly reduce uremic toxins clearance efficiency, especially protein bound uremic toxins and middle molecules. Membrane characteristics such as chemical composition, hydrophilicity, surface roughness, pore size and binding affinity influence the interactions and the attachments between human serum proteins and HD membranes hence they can impact the inflammatory response experienced by HD patients. This study highlighted an innovative investigation on the common HD membrane morphology available in Canadian hospitals, and its affinity for human serum protein attachment. Synchrotron based X-ray imaging techniques available at the Biomedical Imaging and Therapy (BMIT) beamline at the Canadian Light Source (CLS) has answered key questions of HD membrane morphology layer-by-layer and human serum protein transport in membrane channels. This study will highlight the proof that Synchrotron imaging techniques are effective for membrane characterization and protein deposition assessment through both qualitative and quantitative analyses.
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