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首页> 外文期刊>Artificial Organs >On the Use of the Platelet Activity State Assay for the In Vitro Quantification of Platelet Activation in Blood Recirculating Devices for Extracorporeal Circulation
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On the Use of the Platelet Activity State Assay for the In Vitro Quantification of Platelet Activation in Blood Recirculating Devices for Extracorporeal Circulation

机译:血小板活动状态测定在体外循环血液循环装置中血小板活化的体外定量研究中的应用

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We designed an experimental setup to characterize the thrombogenic potential associated with blood recirculating devices (BRDs) used in extracorporeal circulation (ECC). Our methodology relies on in vitro flow loop platelet recirculation experiments combined with the modified-prothrombinase platelet activity state (PAS) assay to quantify the bulk thrombin production rate of circulated platelets, which correlates to the platelet activation (PA) level. The method was applied to a commercial neonatal hollow fiber membrane oxygenator. In analogous hemodynamic environment, we compared the PA level resulting from multiple passes of platelets within devices provided with phosphorylcholine (PC)-coated and noncoated (NC) fibers to account for flow-related mechanical factors (i.e., fluid-induced shear stress) together with surface contact activation phenomena. We report for the first time that PAS assay is not significantly sensitive to the effect of material coating under clinically pertinent flow conditions (500 mL/min), while providing straightforward information on shear-mediated PA dynamics in ECC devices. Being that the latter is intimately dependent on local flow dynamics, according to our results, the rate of thrombin production as measured by the PAS assay is a valuable biochemical marker of the selective contribution of PA in BRDs induced by device design features. Thus, we recommend the use of PAS assay as a means of evaluating the effect of modification of specific device geometrical features and/or different design solutions for developing ECC devices providing flow conditions with reduced thrombogenic impact.
机译:我们设计了一个实验装置来表征与体外循环(ECC)中使用的血液循环装置(BRD)相关的血栓形成潜能。我们的方法依赖于体外流通环血小板再循环实验与改良的凝血酶原血小板活性状态(PAS)分析相结合来量化循环血小板的整体凝血酶产生速率,这与血小板活化(PA)水平相关。该方法被应用于商业新生儿中空纤维膜充氧器。在类似的血液动力学环境中,我们比较了在配有磷胆碱(PC)涂层和未涂层​​(NC)纤维的设备中血小板多次通过后产生的PA水平,以共同考虑与流量相关的机械因素(即,流体引起的剪切应力)具有表面接触活化现象。我们首次报告,在临床相关流量条件下(500 mL / min),PAS分析对材料涂层的影响并不显着敏感,同时提供了有关ECC装置中剪切介导的PA动态的直接信息。由于后者密切依赖于局部流动动力学,因此根据我们的结果,通过PAS分析测定的凝血酶产生速率是PA在设备设计特征引起的BRD中选择性贡献的重要生物化学标记。因此,我们建议使用PAS分析作为评估修改特定设备几何特征和/或不同设计解决方案的效果的方法,以开发可减少血栓形成影响的流动条件的ECC设备。

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