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首页> 外文期刊>Polymer Preprints >INCORPORATING N-VINYL-2-PYRROLIDONE INTO POLYACRYLONITR1LE BY WATER-PHASE PRECIPITATION COPOLYMER1ZATION TO IMPROVE ITS BIOCOMPATIBILITY
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INCORPORATING N-VINYL-2-PYRROLIDONE INTO POLYACRYLONITR1LE BY WATER-PHASE PRECIPITATION COPOLYMER1ZATION TO IMPROVE ITS BIOCOMPATIBILITY

机译:通过水相沉淀共聚合将N-乙烯基-2-吡咯烷酮掺入聚丙烯腈中以改善其生物相容性

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摘要

Polyacrylonitrilc (PAN) and acrylonitrile-based eopolymers have been successfully applied as membrane materials in the fields of dialysis, ultrafiltration, enzyme immobilization and pervaporation. However, because of the relatively poor hydrophilicity and/or biocompatibility for this type of membrane, some additional processes, such as chemical modification, biomacromolecule tethering (e.g. heparin), and cell seeding techniques must be taken to reduce the protein adsorption and prevent the blood clotting in hemodialysis.1 Since both good hemocompatibility and suitable flux are required for hemodialysis membrane, it is important to minimize the membrane-protein interactions which will irreversibly induce the membrane biofouling as well as activate the blood coagulation process. These interactions arc related to the chemical structure, the hydrophilicity/ hydrophobicity balance, the morphology (i.e. the domain structure of a multi-component system), and the topography (i.e. the surface roughness) of the membrane surface.' Af-Vinyl-2-pyrrolidone (NVP) is a potential monomer for the chemical modification of polymeric membranes mainly for its amphiphilic and biocompatible characteristics. It has been reported that poly(iV-vinyl-2-pyrrolidone) (PVP) is an attractive coating material for its superior biocompatibility and lubricity. The coating of PVP can evidently result in improved hemocompatibility with no need to invoke tissue engineering techniques including endothelial cell seeding.2 In addition, this versatile NVP monomer can be easily obtained and has the potential to be used on a large scale.
机译:聚丙烯腈(PAN)和基于丙烯腈的均聚物已成功地用作透析,超滤,酶固定和全蒸发领域的膜材料。但是,由于此类膜的亲水性和/或生物相容性较差,因此必须采取一些其他方法,例如化学修饰,生物大分子束缚(例如肝素)和细胞接种技术,以减少蛋白质的吸附并防止血液进入血液透析中的凝结。1由于血液透析膜既需要良好的血液相容性,又需要合适的通量,因此重要的是要最小化膜蛋白相互作用,这将不可逆转地引起膜生物结垢并激活凝血过程。这些相互作用与膜表面的化学结构,亲水性/疏水性平衡,形态(即多组分体系的畴结构)和形貌(即表面粗糙度)有关。 Af-乙烯基-2-吡咯烷酮(NVP)是潜在的单体,主要由于其两亲性和生物相容性特性而对聚合物膜进行化学修饰。据报道,聚(iV-乙烯基-2-吡咯烷酮)(PVP)由于其优异的生物相容性和润滑性而成为有吸引力的涂料。 PVP涂层显然可以改善血液相容性,而无需调用包括内皮细胞接种在内的组织工程技术。2此外,这种多用途的NVP单体可以轻松获得,并具有大规模使用的潜力。

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