In situ synchrotron quantitative analysis of competitive adsorption tendency of human serum protein to different clinical hemodialysis membranes and assessment of potential impacts

Amira Abdelrasoul , Heloisa Westphalen , Denis Kalugin , Huu Doan , Ahmed Shoker
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Abstract

Protein adsorption on hemodialysis (HD) membrane matrices and surfaces is a highly undesirable process, as it triggers complement activation and leads to severe health complications for HD patients. However, there is a lack of systematic research investigating the correlation between membrane characteristics and their performance in the dialysis process. This study aims to provide a comprehensive understanding of the competitive adsorption tendencies of three human serum proteins (albumin (HSA), fibrinogen (FB), and transferrin (TRF)) on clinical dialysis membranes composed of polyethersulfone (PES), polyacrylonitrile (PAN), and polyvinyl fluoride (PVDF) polymers. To assess membrane morphology across the membrane cross-section, in situ synchrotron radiation micro-computed tomography (SR-µCT) imaging was conducted at the Canadian Light Source (CLS). Protein adsorption was analyzed qualitatively and quantitatively using an innovative synchrotron-based X-ray tomography technique. To determine the mutual influence of protein species on overall protein adsorption, adsorption from single-protein solutions was compared to adsorption from a protein mixture. Regarding single-protein adsorption, the PVDF membrane exhibited 40% less adsorption of HSA compared to the PES membrane. Conversely, FB adsorption was approximately 25% higher on the PVDF membrane compared to the PES membrane. The PAN membrane showed similar levels of HSA adsorption as the PES membrane and similar levels of FB adsorption as the PVDF membrane. In the case of adsorption from the protein mixture, a suppression of HSA adsorption and replacement of HSA with FB were observed. Consequently, the initial solution with a HSA content of 92% resulted in an adsorbed layer containing approximately 75–80% HSA across all the studied membranes. TRF adsorption remained unaffected by the presence of other proteins, consistent across all three membranes. Notably, the PES membrane exhibited the most significant change in the adsorbed protein composition between single-protein and multi-protein adsorption. In addition, this study comprehensively assesses the impact of fibrinogen adsorption on dialysis, including its consequences, blood activation, and implications for quality of life.

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人血清蛋白对不同临床血液透析膜竞争吸附趋势的原位同步定量分析及潜在影响评估
蛋白质吸附在血液透析(HD)膜基质和表面是一个非常不受欢迎的过程,因为它会触发补体激活并导致HD患者严重的健康并发症。然而,对于透析过程中膜特性与其性能之间的关系,目前还缺乏系统的研究。本研究旨在全面了解三种人血清蛋白(白蛋白(HSA)、纤维蛋白原(FB)和转铁蛋白(TRF))在聚醚砜(PES)、聚丙烯腈(PAN)和聚氟乙烯(PVDF)聚合物组成的临床透析膜上的竞争吸附趋势。为了评估膜横截面上的膜形态,在加拿大光源(CLS)下进行了原位同步辐射微计算机断层扫描(SR-µCT)成像。利用一种创新的基于同步加速器的x射线断层扫描技术,对蛋白质吸附进行定性和定量分析。为了确定蛋白质种类对整体蛋白质吸附的相互影响,将单一蛋白质溶液的吸附与蛋白质混合物的吸附进行了比较。在单蛋白吸附方面,PVDF膜对HSA的吸附比PES膜少40%。相反,与PES膜相比,PVDF膜对FB的吸附率约高25%。PAN膜对HSA的吸附量与PES膜相似,对FB的吸附量与PVDF膜相似。在蛋白混合物吸附的情况下,观察到抑制HSA的吸附和用FB代替HSA。因此,HSA含量为92%的初始溶液在所有研究的膜上产生了含有约75-80% HSA的吸附层。TRF的吸附不受其他蛋白质存在的影响,在所有三种膜上都是一致的。值得注意的是,在单蛋白吸附和多蛋白吸附中,PES膜的蛋白质组成变化最为显著。此外,本研究全面评估了纤维蛋白原吸附对透析的影响,包括其后果、血液活化和对生活质量的影响。
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来源期刊
Biomedical engineering advances
Biomedical engineering advances Bioengineering, Biomedical Engineering
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59 days
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