In vitro hemocompatibility screening of a slippery liquid impregnated surface coating for extracorporeal organ support applications

体外循环 离体 血栓 医学 体外 生物医学工程 纤维蛋白原 蛋白质吸附 全血 聚氯乙烯 粘附 血小板活化 血小板 外科 聚合物 材料科学 体外 化学 生物化学 免疫学 复合材料 内科学
作者
Teryn R Roberts,Raymond P. Seekell,Yanyi Zang,George T Harea,Zheng Zhang,Andriy I. Batchinsky
出处
期刊:Perfusion [SAGE]
卷期号:39 (1): 76-84 被引量:4
标识
DOI:10.1177/02676591221095469
摘要

Clot formation, infection, and biofouling are unfortunate but frequent complications associated with the use of blood-contacting medical devices. The challenge of blood-foreign surface interactions is exacerbated during medical device applications involving substantial blood contact area and extended duration of use, such as extracorporeal life support (ECLS). We investigated a novel surface modification, a liquid-impregnated surface (LIS), designed to minimize protein adsorption and thrombus development on medical plastics.The hemocompatibility and efficacy of LIS was investigated first in a low-shear model with LIS applied to the lumen of blood incubation vials and exposed to human whole blood. Additionally, LIS was evaluated in a 6 h ex vivo circulation model with swine blood using full-scale ECLS circuit tubing and centrifugal pumps with clinically relevant flow rate (1.5 L/min) and shear conditions for extracorporeal carbon dioxide removal.Under low-shear, LIS preserved fibrinogen concentration in blood relative to control polymers (+40 ± 6 mg/dL vs polyvinyl chloride, p < .0001), suggesting protein adsorption was minimized. A fibrinogen adhesion assay demonstrated a dramatic reduction in protein adsorption under low shear (87% decrease vs polyvinyl chloride, p = .01). Thrombus deposition and platelet adhesion visualized by scanning electron microscopy were drastically reduced. During the 6 h ex vivo circulation, platelets in blood exposed to LIS tubing did not become significantly activated or procoagulant, as occurred with control tubing; and again, thrombus deposition was visually reduced.A LIS coating demonstrated potential to reduce thrombus formation on medical devices. Further testing is needed specialized to clinical setting and duration of use for specific medical target applications.
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