Key Laboratory of Textile Science & Technology, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620, China.
State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620, China.
J Colloid Interface Sci. 2017 Nov 15;506:442-451. doi: 10.1016/j.jcis.2017.07.060. Epub 2017 Jul 18.
Construction ion-exchange membranes with superb biomolecules adsorption and purification performance plays a greatly important role in the fields of biotechnological and biopharmaceutical industry, yet still remains an extremely challenging. Herein, we in situ synthesized the cis-butenedioic anhydride grafted poly(vinyl alcohol) hydrogel nanofibrous membranes (CBA-g-PVA HNFM) by combining electrospinning technique with the grafting-copolymerization crosslinking. Taking advantages of the large specific surface area which could provide numerous sites available for functional groups and biomolecules binding, highly tortuous and interconnected porous channel for biomolecules transfer, and enhanced mechanical strength, the resultant CBA-g-PVA HNFM exhibited relatively high binding amount of 170mgg, rapid equilibrium time of 8h towards the biomolecule template of lysozyme, and the performance could be tailored by regulating the buffer properties and protein concentrations. Additionally, the resultant functional HNFM also possessed superior acid resistance property, excellent reversibility and regeneration performance. More importantly, the obtained CBA-g-PVA HNFM could directly extract lysozyme from fresh chicken eggs with capacity of 125mgg, exhibiting excellent practical application properties. The fabrication of proposed CBA-g-PVA HNFM offers a feasible alternative for construction of ion-exchange chromatograph column for bio-separation and purification engineering.
原位合成顺丁烯二酸酐接枝聚乙烯醇水凝胶纳米纤维膜(CBA-g-PVA HNFM),通过静电纺丝技术与接枝共聚交联相结合。利用大的比表面积为功能基团和生物分子结合提供大量的结合位点、高度曲折和相互连接的多孔通道用于生物分子传递,以及增强的机械强度,所得的 CBA-g-PVA HNFM 对溶菌酶等生物分子模板具有相对较高的结合量(170mgg)、快速平衡时间(8h),并且可以通过调节缓冲性质和蛋白质浓度来调整其性能。此外,所得功能化 HNFM 还具有优异的耐酸性、良好的可恢复性和再生性能。更重要的是,所获得的 CBA-g-PVA HNFM 可以直接从新鲜鸡蛋中提取溶菌酶,容量为 125mgg,表现出优异的实际应用性能。所提出的 CBA-g-PVA HNFM 的制备为生物分离和纯化工程中的离子交换色谱柱的构建提供了一种可行的替代方案。