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在聚醚砜膜基底上引入多种生物功能基团,构建有效的抗血栓生物界面。

Introducing multiple bio-functional groups on the poly(ether sulfone) membrane substrate to fabricate an effective antithrombotic bio-interface.

机构信息

Jiangsu Provincial Key Laboratory for Interventional Medical Devices. Huaiyin Institute of Technology, Huaian 223003, China.

出版信息

Biomater Sci. 2017 Nov 21;5(12):2416-2426. doi: 10.1039/c7bm00673j.

Abstract

It has been widely recognized that functional groups on biomaterial surfaces play important roles in blood compatibility. To construct an effective antithrombotic bio-interface onto the poly(ether sulfone) (PES) membrane surface, bio-functional groups of sodium carboxylic (-COONa), sodium sulfonic (-SONa) and amino (-NH) groups were introduced onto the PES membrane surface in three steps: the synthesis of PES with carboxylic (-COOH) groups (CPES) and water-soluble PES with sodium sulfonic (-SONa) groups and amino (-NH) groups (SNPES); the introduction of carboxylic groups onto the PES membrane by blending CPES with PES; and the grafting of SNPES onto CPES/PES membranes via the coupling of amino groups and carboxyl groups. The physical/chemical properties and bioactivities were dependent on the proportions of the additives. After introducing bio-functional groups, the excellent hemocompatibility of the modified membranes was confirmed by the inhibited platelet adhesion and activation, prolonged clotting times, suppressed blood-related complement and leukocyte-related complement receptor activations. Furthermore, cell tests indicated that the modified membranes showed better cytocompatibility in endothelial cell proliferation than the pristine PES membrane due to the synergistic promotion of the functional groups. To sum up, these results suggested that modified membranes present great potential in fields using blood-contacting materials, such as hemodialysis and surface endothelialization.

摘要

人们普遍认识到,生物材料表面的官能团在血液相容性中起着重要作用。为了在聚醚砜(PES)膜表面构建有效的抗血栓生物界面,通过三个步骤将生物官能团的羧酸钠(-COONa)、磺酸钠(-SONa)和氨基(-NH)基团引入 PES 膜表面:合成具有羧基(-COOH)基团的 PES(CPES)和具有水溶性的磺酸钠(-SONa)和氨基(-NH)基团的 PES(SNPES);通过 CPES 与 PES 共混将羧基引入 PES 膜;通过氨基和羧基的偶联将 SNPES 接枝到 CPES/PES 膜上。物理/化学性质和生物活性取决于添加剂的比例。引入生物官能团后,通过抑制血小板黏附和激活、延长凝血时间、抑制血液相关补体和白细胞相关补体受体激活,证实了改性膜具有优异的血液相容性。此外,细胞试验表明,由于官能团的协同促进作用,改性膜在促进内皮细胞增殖方面比原始 PES 膜具有更好的细胞相容性。总之,这些结果表明,改性膜在使用与血液接触的材料的领域,如血液透析和表面内皮化,具有巨大的潜力。

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