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Protein-polymer interaction: Transfer loading at interfacial region of PES-based membrane and BSA

机译:蛋白质 - 聚合物相互作用:在基于PES的膜和BSA的界面区域转移负载

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摘要

The adsorption of proteins onto polymeric surfaces is encountered in many natural and industrial processes and is a prerequisite to their efficient identification, separation, and purification by methods such as chromatography, and filtration. Nevertheless, the exact nature of the adsorption mechanisms and interfacial interactions is not easy to identify for a given protein-polymer system. Here, we aim to document the adsorption mechanism of a protein-polymer system by investigating the adsorption as well as desorption phenomenon of a protein [bovine serum albumin (BSA)] from the polymeric surface [polyethersulfone (PES)]. The analyses performed to document the adsorption mechanism of the BSA-PES system include scanning electron microscope (SEM), attenuated total reflection-Fourier transform infrared (FTIR), contact angle, zeta potential, surface charge density measurement, and Derjaguin-Landau-Verwey-Overbeek (DLVO). Here, SEM and FTIR identified the physical and chemical properties of pure PES and PES-BSA membranes. The low water contact angle of the PES-BSA membrane confirms its applicability for tissue engineering applications. Further, the zeta potential, surface charge density measurement, and DLVO analyses were performed to document the adsorption mechanism. The adsorption of BSA particles on the PES surface was carried out for pH values that ranged from 4 to 10 for contact times that ranged from 1 to 3 days. A monotonic increase in the zeta potential of the PES-BSA system indicated considerable adsorption of BSA particles on the PES surface. Further, BSA adsorption was very strong for pH values greater than 4.7 which confirms to strong electrostatic interactions between BSA and PES. The strong electrostatic interaction is also collaborated by low desorption rate, which was only similar to 22% for pH 10 after 3 days of contact. (c) 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019, 136, 47931.
机译:蛋白质到聚合物表面上的吸附在许多天然的和工业生产过程中遇到并且是通过诸如层析和过滤的先决条件,以他们的有效识别,分离和纯化。然而,吸附机制和界面相互作用的确切性质是不容易的,以确定一个给定的蛋白质 - 聚合物系统。在这里,我们的目标是通过调查吸附以及蛋白质的解吸现象来记录蛋白质 - 聚合物体系的吸附机理[牛血清白蛋白(BSA)]从聚合物表面[聚醚砜(PES)。这些分析进行,以记录BSA-PES系统的吸附机构包括扫描电子显微镜(SEM),衰减全反射傅里叶变换红外(FTIR),接触角,ζ电位,表面电荷密度的测量,并且Derjaguin-的Landau-维韦-Overbeek(DLVO)。在这里,扫描电镜和红外光谱鉴定纯PES和PES-BSA膜的物理和化学性质。该PES-BSA膜的低水接触角证实其用于组织工程应用的适用性。此外,进行了ζ电位,表面电荷密度的测量,和分析DLVO记录吸附机理。该PES表面上BSA颗粒的吸附对于范围从4至10为介于1至3天的接触时间的pH值下进行。在PES-BSA系统的ζ电势单调增加表明相当大的吸附的PES表面上BSA颗粒。此外,BSA吸附是用于pH值大于4.7,其确认与BSA和PES之间的强静电相互作用很强。强静电相互作用也由低解吸速率,这是只接触后3天类似于22%用于pH 10合作。 (c)2019 Wiley期刊,Inc.J.Phill。聚合物。 SCI。 2019年,136,47931。

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