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内源性一氧化氮释放微凝胶涂层可防止暴露于体外血流的氧合器纤维上形成凝块。

Endogenous Nitric Oxide-Releasing Microgel Coating Prevents Clot Formation on Oxygenator Fibers Exposed to In Vitro Blood Flow.

作者信息

Winnersbach Patrick, Hosseinnejad Aisa, Breuer Thomas, Fechter Tamara, Jakob Felix, Schwaneberg Ulrich, Rossaint Rolf, Bleilevens Christian, Singh Smriti

机构信息

Department of Anesthesiology, University Hospital RWTH Aachen, Pauwelsstraße 30, 52074 Aachen, Germany.

DWI-Leibniz-Institute for Interactive Materials e.V., Forckenbeckstr. 50, 52056 Aachen, Germany.

出版信息

Membranes (Basel). 2022 Jan 6;12(1):73. doi: 10.3390/membranes12010073.

Abstract

BACKGROUND

Clot formation on foreign surfaces of extracorporeal membrane oxygenation systems is a frequent event. Herein, we show an approach that mimics the enzymatic process of endogenous nitric oxide (NO) release on the oxygenator membrane via a biomimetic, non-fouling microgel coating to spatiotemporally inhibit the platelet (PLT) activation and improve antithrombotic properties. This study aims to evaluate the potential of this biomimetic coating towards NO-mediated PLT inhibition and thereby the reduction of clot formation under flow conditions.

METHODS

Microgel-coated (NOrel) or bare (Control) poly(4-methyl pentene) (PMP) fibers were inserted into a test channel and exposed to a short-term continuous flow of human blood. The analysis included high-resolution PLT count, pooled PLT activation via β-Thromboglobulin (β-TG) and the visualization of remnants and clots on the fibers using scanning electron microscopy (SEM).

RESULTS

In the Control group, PLT count was significantly decreased, and β-TG concentration was significantly elevated in comparison to the NOrel group. Macroscopic and microscopic visualization showed dense layers of stable clots on the bare PMP fibers, in contrast to minimal deposition of fibrin networks on the coated fibers.

CONCLUSION

Endogenously NO-releasing microgel coating inhibits the PLT activation and reduces the clot formation on PMP fibers under dynamic flow.

摘要

背景

体外膜肺氧合系统的外来表面形成凝块是常见现象。在此,我们展示了一种方法,即通过仿生、防污微凝胶涂层模拟氧合器膜上内源性一氧化氮(NO)释放的酶促过程,以时空方式抑制血小板(PLT)活化并改善抗血栓性能。本研究旨在评估这种仿生涂层对NO介导的PLT抑制作用的潜力,从而减少流动条件下的凝块形成。

方法

将微凝胶涂层(NOrel)或裸露(对照)的聚(4-甲基戊烯)(PMP)纤维插入测试通道,并使其暴露于短期连续流动的人血中。分析包括高分辨率PLT计数、通过β-血小板球蛋白(β-TG)进行的汇总PLT活化以及使用扫描电子显微镜(SEM)对纤维上的残留物和凝块进行可视化。

结果

与NOrel组相比,对照组的PLT计数显著降低,β-TG浓度显著升高。宏观和微观可视化显示,裸露的PMP纤维上有致密的稳定凝块层,而涂层纤维上的纤维蛋白网络沉积极少。

结论

内源性释放NO的微凝胶涂层在动态流动条件下可抑制PLT活化并减少PMP纤维上的凝块形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c56e/8779597/c5ef8f523ae4/membranes-12-00073-sch001.jpg

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