Modification of a PES microfiltration membrane to enhance sterile filtration by inhibiting protein adsorption

微滤 吸附 过滤(数学) 原子转移自由基聚合 化学 蛋白质吸附 色谱法 结垢 表面改性 共聚物 材料科学 接触角 膜污染 两亲性 高分子化学 化学工程 生物化学 聚合物 有机化学 工程类 数学 统计
作者
Kang Hee Yun,Komal Sharma,Hyun Uk Kim,Tae‐Hyun Bae
出处
期刊:Journal of Industrial and Engineering Chemistry [Elsevier BV]
卷期号:123: 311-319 被引量:20
标识
DOI:10.1016/j.jiec.2023.03.048
摘要

Microfiltration membranes are increasingly used in sterilization processes in the pharmaceutical industry. However, in the pharmaceutical industry, product loss caused by the adsorption of high value-added proteins to membranes during the sterilization process is a critical problem. Hence, it is necessary to reduce protein adsorption and fouling through the hydrophilic modification of the entire membrane, not just the surface. We developed a method for fabricating a porous poly(ethersulfone) (PES) microfiltration membrane using vapor-induced phase separation (VIPS) and then conducting hydrophilic modification of the membrane. Two types of symmetric membranes with 0.2 μm pores were prepared using two different additives, one of which was an amphiphilic copolymer (Pluronic® PE6400) that is known to increase the hydrophilicity of PES membranes. Both membranes had high water permeability and suitable mechanical strength. However, protein filtration testing, including an adsorption study, revealed that the hydrophilicity imparted by Pluronic was not sufficient to effectively inhibit protein adhesion. In contrast, the modification via the atom transfer radical polymerization of a hydrophilic oligomer (poly(ethyleneglycol) methacrylate) significantly increased the hydrophilicity of the entire membrane while reducing the surface roughness. These properties reduced protein adsorption and membrane fouling, to the benefit of sterile filtration and protein filtration processes.
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