用于微血管创伤性凝血建模的芯片损伤技术。

IF 6.1 2区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS
Lab on a Chip Pub Date : 2025-01-28 DOI:10.1039/d4lc00471j
Halston Deal, Elizabeth M Byrnes, Sanika Pandit, Anastasia Sheridan, Ashley C Brown, Michael Daniele
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引用次数: 0

摘要

血液凝固是一种高度调控的损伤反应,其特征是纤维蛋白纤维的聚合,以阻止血液从受损的血管内皮通过。越来越多的研究试图监测微流体系统中的凝血,但未能捕捉到凝血作为对血管内皮破坏的反应。在这里,我们提出了一种装置,允许压缩损伤的微流控血管内皮的一个确定的部分和损伤部位的凝血评估。这种压力损伤芯片(PINCH)设备允许可视化凝血作为荧光纤维蛋白在损伤部位的积累。损伤上游和损伤部位的荧光纤维蛋白水平的定量证实,用流体剪切应力预处理血管内皮有助于捕获凝血作为损伤反应。我们利用PINCH设备来证明A型血友病患者的有限凝血反应,并评估止血微粒和纤溶纳米颗粒的性能。我们的研究结果和PINCH装置的直接制造使其成为止血治疗的额外筛选的有希望的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Injury-on-a-chip for modelling microvascular trauma-induced coagulation.

Blood coagulation is a highly regulated injury response that features polymerization of fibrin fibers to prevent the passage of blood from a damaged vascular endothelium. A growing body of research seeks to monitor coagulation in microfluidic systems but fails to capture coagulation as a response to disruption of the vascular endothelium. Here we present a device that allows compression injury of a defined segment of a microfluidic vascular endothelium and the assessment of coagulation at the injury site. This pressure injury-on-a-chip (PINCH) device allows visualization of coagulation as the accumulation of fluorescent fibrin at injury sites. Quantification of fluorescent fibrin levels upstream of and at injury sites confirm that pre-treating vascular endothelium with fluid shear stress helps capture coagulation as an injury response. We leverage the PINCH devices to demonstrate the limited coagulation response of type A hemophiliacs and evaluate the performance of hemostatic microparticles and fibrinolytic nanoparticles. Our findings and the straightforward fabrication of the PINCH devices make it a promising choice for additional screening of hemostatic therapeutics.

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来源期刊
Lab on a Chip
Lab on a Chip 工程技术-化学综合
CiteScore
11.10
自引率
8.20%
发文量
434
审稿时长
2.6 months
期刊介绍: Lab on a Chip is the premiere journal that publishes cutting-edge research in the field of miniaturization. By their very nature, microfluidic/nanofluidic/miniaturized systems are at the intersection of disciplines, spanning fundamental research to high-end application, which is reflected by the broad readership of the journal. Lab on a Chip publishes two types of papers on original research: full-length research papers and communications. Papers should demonstrate innovations, which can come from technical advancements or applications addressing pressing needs in globally important areas. The journal also publishes Comments, Reviews, and Perspectives.
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