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纤维蛋白在心血管生物材料和医疗器械上的吸附。

Fibrin Adsorption on Cardiovascular Biomaterials and Medical Devices.

机构信息

Department of Chemistry, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark.

Department of Civil and Mechanical Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark.

出版信息

ACS Appl Bio Mater. 2023 Jul 17;6(7):2667-2676. doi: 10.1021/acsabm.2c01057. Epub 2023 Jun 27.

Abstract

Medical devices that are inserted in blood vessels always risk eliciting thrombosis, and the surface properties of such devices are thus of major importance. The initiating step for surface-induced pathological coagulation has been associated with adsorption of fibrinogen protein on biomaterial surfaces and subsequent polymerization into an insoluble fibrin clot. This issue gives rise to an inherent challenge in biomaterial design as varied surface materials must fulfill specialized roles while also minimizing thrombotic complications from spontaneous fibrin(ogen) recruitment. We have aimed to characterize the thrombogenic properties of state-of-the-art cardiovascular biomaterials and medical devices by quantifying the relative surface-dependent adsorption and formation of fibrin followed by analysis of the resulting morphologies. We identified stainless steel and amorphous fluoropolymer as comparatively preferable biomaterials based on their low fibrin(ogen) recruitment, in comparison to other metallic and polymeric biomaterials, respectively. In addition, we observed a morphological trend that fibrin forms fiber structures on metallic surfaces and fractal branched structures on polymeric surfaces. Finally, we used vascular guidewires as clotting substrates and found that fibrin adsorption depends on parts of the guidewire that are exposed, and we correlated the morphologies on uncoated guidewires with those formed on raw stainless-steel biomaterials.

摘要

医疗器械插入血管时总是存在引发血栓的风险,因此这些器械的表面特性非常重要。表面诱导的病理凝血的起始步骤与纤维蛋白原蛋白在生物材料表面的吸附以及随后聚合形成不溶性纤维蛋白凝块有关。这个问题在生物材料设计中带来了一个固有挑战,因为各种表面材料必须满足特殊的角色,同时最小化自发纤维蛋白(原)募集引起的血栓并发症。我们旨在通过定量分析纤维蛋白的相对表面依赖性吸附和形成来表征最先进的心血管生物材料和医疗器械的血栓形成特性,然后分析由此产生的形态。我们确定不锈钢和无定形氟聚合物是比较理想的生物材料,因为它们与其他金属和聚合物生物材料相比,对纤维蛋白(原)的募集作用较低。此外,我们观察到纤维蛋白在金属表面形成纤维结构,在聚合物表面形成分形分支结构的形态趋势。最后,我们将血管导丝用作凝血底物,发现纤维蛋白吸附取决于暴露的导丝部分,并将未涂层导丝上的形态与原始不锈钢生物材料上形成的形态进行了关联。

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