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聚醚型硅烷两亲性改性聚氨酯的抗血栓性能

Thromboresistance of Polyurethanes Modified with PEO-Silane Amphiphiles.

机构信息

Department of Biomedical Engineering, Texas A&M University, College Station, TX, 77843, USA.

Department of Medical Physiology, Texas A&M University Health Science Center, Bryan, TX, 77807, USA.

出版信息

Macromol Biosci. 2020 Dec;20(12):e2000193. doi: 10.1002/mabi.202000193. Epub 2020 Aug 18.

DOI:10.1002/mabi.202000193
PMID:32812374
Abstract

Surface-induced thrombosis is problematic in blood-contacting devices composed of silicones or polyurethanes (PUs). Poly(ethylene oxide)-silane amphiphiles (PEO-SA) are previously shown effective as surface modifying additives (SMAs) in silicones for enhanced thromboresistance. This study investigates PEO-SAs as SMAs in a PU at various concentrations: 5, 10, 25, 50, and 100 µmol g PU. PEO-SA modified PUs are evaluated for their mechanical properties, water-driven surface restructuring, and adhesion resistance against a human fibrinogen (HF) solution as well as whole human blood. Stability is assessed by monitoring hydrophilicity, water uptake, and mass loss following air- or aqueous-conditioning. PEO-SA modified PUs do not demonstrate plasticization, as evidenced by minimal changes in glass transition temperature, modulus, tensile strength, and percent strain at break. These also show a concentration-dependent increase in hydrophilicity that is sustained following air- and aqueous-conditioning for concentrations ≥25 µmol g . Additionally, water uptake and mass loss are minimal at all concentrations. Although protein resistance is not enhanced versus an HF solution, PEO-SA modified PUs have significantly reduced protein adsorption and platelet adhesion from human blood at concentrations ≥10 µmol g . Overall, this study demonstrates the versatility of PEO-SAs as SMAs in PU, which leads to enhanced and sustained hydrophilicity as well as thromboresistance.

摘要

表面诱导的血栓形成是由硅橡胶或聚氨基甲酸酯(PU)组成的与血液接触的器械的一个问题。聚(环氧乙烷)-硅烷两亲物(PEO-SA)以前被证明是硅橡胶中作为表面改性添加剂(SMA)有效的,可增强抗血栓性。本研究研究了 PEO-SA 在不同浓度(5、10、25、50 和 100µmol g PU)下作为 PU 中的 SMA 的性能。评估了 PEO-SA 改性的 PU 的机械性能、水驱动的表面重构、以及对人纤维蛋白原(HF)溶液和全血的抗粘附性。通过监测亲水性、水吸收和空气或水条件下的质量损失来评估稳定性。PEO-SA 改性的 PU 没有表现出增塑作用,这表现为玻璃化转变温度、模量、拉伸强度和断裂伸长率的最小变化。这些也表现出随浓度增加的亲水性增加,在空气和水条件下均保持稳定,浓度≥25µmol g。此外,在所有浓度下水吸收和质量损失都很小。尽管与 HF 溶液相比,蛋白质的抗阻性没有提高,但 PEO-SA 改性的 PU 在浓度≥10µmol g时,从人血中显著减少了蛋白质吸附和血小板粘附。总的来说,本研究表明 PEO-SA 作为 PU 中的 SMA 的多功能性,可导致增强和持久的亲水性以及抗血栓性。

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