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体外人凝血酶生成模型中 p48 和抗血栓形成的 p48 亲水聚合物涂层低剖面血流分流器的血栓形成性。

Thrombogenicity of the p48 and anti-thrombogenic p48 hydrophilic polymer coating low-profile flow diverters in an in vitro human thrombin generation model.

机构信息

The Royal London Hospital, London, UK.

Phenox GmbH, Bochum, Germany.

出版信息

Interv Neuroradiol. 2020 Aug;26(4):488-493. doi: 10.1177/1591019920923817. Epub 2020 May 4.

Abstract

OBJECTIVES

The implantation of flow diverters, or stents in general, necessitates the use of dual anti-platelet treatment with typical regimes including aspirin and a P2Y12 inhibitor. This carries an inherent risk of haemorrhage. We sought to compare the thrombogenicity of the anti-thrombogenic p48 hydrophilic polymer coating compared to the standard uncoated p48 flow diverter using an in vitro thrombogenicity assay.

METHODS

To evaluate the thrombin generation influenced by the different stent types the stents were placed in wells of a 24-well plate with the addition of plasma from healthy volunteers the thrombin calibrator respectively the PPP-reagent was added. Subsequently, the thrombin substrate was added and the thrombin generation was analysed every 60 s using a thrombinoscope. The assay is calibrated using samples containing a known amount of active thrombin in PPP. Thrombin activity is proportional to the change in fluorescence.

RESULTS

The p48 hydrophilic polymer coating shows a significantly lower peak thrombin concentration (1.13 ± 0.21 vs. 1.41 ± 0.22) and longer time to peak thrombin concentration (0.96 ± 0.04 vs. 0.74 ± 0.07) compared to the uncoated p48 device ( < 0.01). The responses of the p48 hydrophilic polymer coating were similar to that of the negative control.

CONCLUSION

The hydrophilic polymer coating surface modification significantly reduces the thrombogenicity of the p48 flow diverter. These results corroborate the findings from previous in vitro studies.

摘要

目的

植入血流导向装置(或支架)通常需要使用双重抗血小板治疗,典型方案包括阿司匹林和 P2Y12 抑制剂。这会带来出血的固有风险。我们试图通过体外血栓形成试验比较抗血栓形成的 p48 亲水聚合物涂层与标准未涂层 p48 血流导向器的血栓形成性。

方法

为了评估不同支架类型对凝血酶生成的影响,将支架放置在 24 孔板的孔中,加入来自健康志愿者的血浆、凝血酶校准器和 PPP 试剂。随后,加入凝血酶底物,并使用凝血酶仪每 60 秒分析一次凝血酶生成。该测定使用 PPP 中含有已知量活性凝血酶的样品进行校准。凝血酶活性与荧光变化成正比。

结果

p48 亲水聚合物涂层的峰值凝血酶浓度明显较低(1.13±0.21 比 1.41±0.22),达到峰值凝血酶浓度的时间也较长(0.96±0.04 比 0.74±0.07),与未涂层的 p48 装置相比(<0.01)。p48 亲水聚合物涂层的反应与阴性对照相似。

结论

亲水聚合物涂层表面改性显著降低了 p48 血流导向器的血栓形成性。这些结果与之前的体外研究结果一致。

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