透析
血液透析
膜
人工肾
透析管
尿毒症毒素
化学
补体系统
凝结
蛋白质吸附
吸附
医学
生物医学工程
免疫系统
外科
生物化学
内科学
免疫学
有机化学
作者
Adam M. Zawada,Thomas Lang�,Bertram Ottillinger,Fatih Kırçelli,Manuela Stauss‐Grabo,James Kennedy
出处
期刊:Membranes
[Multidisciplinary Digital Publishing Institute]
日期:2022-09-26
卷期号:12 (10): 932-932
被引量:35
标识
DOI:10.3390/membranes12100932
摘要
The dialyzer is the core element in the hemodialysis treatment of patients with end-stage kidney disease (ESKD). During hemodialysis treatment, the dialyzer replaces the function of the kidney by removing small and middle-molecular weight uremic toxins, while retaining essential proteins. Meanwhile, a dialyzer should have the best possible hemocompatibility profile as the perpetuated contact of blood with artificial surfaces triggers complement activation, coagulation and immune cell activation, and even low-level activation repeated chronically over years may lead to undesired effects. During hemodialysis, the adsorption of plasma proteins to the dialyzer membrane leads to a formation of a secondary membrane, which can compromise both the uremic toxin removal and hemocompatibility of the dialyzer. Hydrophilic modifications of novel dialysis membranes have been shown to reduce protein adsorption, leading to better hemocompatibility profile and performance stability during dialysis treatments. This review article focuses on the importance of performance and hemocompatibility of dialysis membranes for the treatment of dialysis patients and summarizes recent studies on the impact of protein adsorption and hydrophilic modifications of membranes on these two core elements of a dialyzer.
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