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Heparinized Polyurethane Surface Via a One-Step Photografting Method

机译:一步接枝法肝素化聚氨酯表面

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摘要

Traditional methods using coupling chemistry for surface grafting of heparin onto polyurethane (PU) are disadvantageous due to their generally low efficiency. In order to overcome this problem, a quick one-step photografting method is proposed here. Three heparin derivatives incorporating 0.21, 0.58, and 0.88 wt% pendant aryl azide groups were immobilized onto PU surfaces, leading to similar grafting densities of 1.07, 1.17, and 1.13 μg/cm2, respectively, yet with increasing densities of anchoring points. The most negatively charged surface and the maximum binding ability towards antithrombin III were found for the heparinized PU with the lowest amount of aryl azide/anchor sites. Furthermore, decreasing the density of anchoring points was found to inhibit platelet adhesion to a larger extent and to prolong plasma recalcification time, prothrombin time, thrombin time, and activated partial thromboplastin time to a larger extent. This was also found to enhance the bioactivity of immobilized heparin from 22.9% for raw heparin to 36.9%. This could be explained by the enhanced molecular mobility of immobilized heparin when it is more loosely anchored to the PU surface, as well as a higher surface charge.
机译:使用偶联化学方法将肝素表面接枝到聚氨酯(PU)上的传统方法由于其效率通常较低而不利。为了克服这个问题,在此提出一种快速的一步接枝方法。将三个掺有0.21、0.58和0.88 wt%芳基叠氮化物侧基的肝素衍生物固定在PU表面上,分别得到相似的接枝密度1.07、1.17和1.13μg/ cm 2 ,但是锚点密度的增加。对于具有最小量的芳基叠氮化物/锚定位点的肝素化的PU,发现带负电最多的表面和对抗凝血酶III的最大结合能力。此外,发现降低锚定点的密度可在更大程度上抑制血小板粘附,并在更大程度上延长血浆再钙化时间,凝血酶原时间,凝血酶时间和活化的部分凝血活酶时间。还发现这将固定化肝素的生物活性从原肝素的22.9%提高到36.9%。固定化肝素更松散地锚定到PU表面时,分子移动性增强,并且表面电荷较高,可以解释这点。

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