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A New Polysulfone Membrane Dialyzer, NV, with Low-Fouling and Antithrombotic Properties

机译:一种新的聚砜膜透析仪,NV,具有低污染和抗血栓性能

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Background: The biggest problem in routine hemodialy-sis therapy is possibly the blood pressure fall experienced by patients during dialysis. In contrast, in medium- and long-term hemodialysis therapy, the main problem might be deterioration of arteriosclerosis because of medial calcification associated with dialysis vintage. Both problems are caused by an autonomic imbalance or structural change in the blood vessels. Inflammation due to extra-corporeal blood circulation is another possible cause. This inflammation is considered to cause platelets activated by contact and adherence with the membrane surface to aggregate with white blood cells and attack the endotheli-um of the blood vessels. Therefore, we tried to develop a new membrane with no adsorption and no platelet activation. Summary: Polysulfone (PS) membranes with polyvi-nylpyrrolidone (PVP) as a hydrophilic agent are widely used in dialysis, but blood components adhere to the membrane surface. We developed a new dialyzer, NV, by localizing a new hydrophilic polymer onto the inner surface of a hollow-fiber membrane composed of PS and PVP. The number of platelets that adhered to the NV membrane surface drastically decreased to 0.9% of that with the conventional PS dialysis membrane. We also confirmed the mechanism by which NV realizes clinical improvements in blood pressure drops and inflammation during dialysis, and verified its clinical appeal. Key Mes-sages:The new membrane NV, which inhibits platelet adhesion and is compatible with blood vessels, is clinically beneficial.
机译:背景:常规血液透析治疗中最大的问题可能是患者在透析期间经历的血压下降。相比之下,在中期和长期血液透析治疗中,由于与透析复古相关的内侧钙化,主要问题可能是动脉硬化的恶化。这两个问题都是由血管的自主性失衡或结构变化引起的。由于积分血液循环导致的炎症是另一种可能的原因。这种炎症被认为是通过接触和粘附与膜表面激活的血小板与白细胞聚集并攻击血管内皮骨。因此,我们试图开发一种没有吸附和血小板活化的新膜。发明内容:具有多维 - 邻吡咯烷酮(PVP)作为亲水剂的聚砜(PS)膜广泛用于透析,但血液成分粘附到膜表面上。我们通过将新的亲水聚合物定位到由PS和PVP组成的中空纤维膜的内表面上,开发了一种新的透析仪NV。粘附到NV膜表面的血小板的数量随着常规PS透析膜的常规PS透析膜的0.9%。我们还确认了NV在透析期间实现血压下降和炎症的临床改善的机制,并验证了其临床吸引力。关键MES鼠标:抑制血管粘附并与血管相容的新膜NV是临床有益的。

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