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Combination of two antithrombogenic methodologies for preventing thrombus formation on a poly(ether ether ketone) substrate

机译:两种抗血栓形成方法的组合预防聚(醚醚酮)底物血栓形成

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摘要

To enhance the total antithrombogenicity of poly(ether ether ketone) (PEEK), we examined a combination of two methodologies for the suppression of activation in both the platelet and coagulation systems. A random copolymer (PMT) composed of a zwitterionic 2-methacryloyloxyethyl phosphorylcholine (MPC) unit and a cationic 2-methacryloyloxyethyl trimethylammonium chloride (TMAEMA) unit was grafted onto the PEEK surface by photoinduced self-initiated graft polymerization of the PEEK substrate (PMTx-g-PEEK). Then, negatively charged heparin was immobilized by ionic binding with TMAEMA units (Hep/PMTx-g-PEEK). The TMAEMA unit composition on grafted PMT altered the surface zeta-potentials of the PEEK substrates. Amounts of immobilized heparin depended on the zeta-potential. The concentration of heparin became constant on the sample surface where the TMAEMA unit composition was 30% or more, and was approximately 2.0 mu g/cm(2). The Hep/PMTx-g-PEEK with a TMAEMA unit composition of 50% showed not only decreased platelet adhesion, but also a 4-fold extension of the blood coagulation time of the poly(MPC)-g-PEEK substrate. The poly(MPC) layer could inhibit platelet adhesion and activation, resulting in surface antithrombogenic properties. Additionally, heparin released from the Hep/PMTx-g-PEEK prevented activation of the coagulation system in whole blood. Therefore, the combination of these antithrombogenic methodologies was promising for prolonging the blood coagulation period of the materials.
机译:为了增强聚(醚醚酮)(PEEK)的总抗动血栓形成性,我们检查了两种方法的组合,用于抑制血小板和凝血系统中的活化。通过PEEK底物的光诱导的自引发接枝聚合接枝由两性离子2-甲基丙烯酰氧基乙基磷素(MPC)单元和阳离子2-甲基丙烯酰氧基甲基三甲基氯化铵(TMAEMA)单元组成的随机共聚物(PMT)通过PEEK底物(PMTX- G-PEEK)。然后,通过与TMAEMA单元(HEP / PMTX-G-PEEK)离子结合来固定带负电荷的肝素。接枝PMT的TMAEMA单元组成改变了PEEK基材的表面Zeta电位。固定化肝素的量依赖于Zeta潜力。肝素的浓度在样品表面上变得恒定,其中TMAEMA单元组合物为30%以上,并且约为2.0μg/ cm(2)。具有50%的TMAEMA单元组成的HEP / PMTX-G-PEEK不仅表现出降低血小板粘附性,而且延长了聚(MPC)-G-PEEK底物的血液凝固时间的4倍。聚(MPC)层可以抑制血小板粘附和活化,导致表面抗凝血性性质。此外,肝素从HEP / PMTX-G-P-P-PEEK中释放,防止了全血的凝血系统的激活。因此,这些抗血栓形成方法的组合是延长材料的血液凝固时期。

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