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Preparation of weak anion exchange chromatographic packings based on monodisperse polymer beads and their application in the separation of bioploymers

机译:基于单分散聚合物珠的弱阴离子交换色谱填料的制备及其在生物聚合物分离中的应用

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摘要

Based on the 8.0 mu m monodisperse, macroporous poly-(glycidylmethacrylate-co-ethylene-dimethacrylate) beads (P-GMA/EDMA), a new hydrophilic weak anion-exchange (WAX) stationary phase for HPLC was synthesized by a new chemically modified method. The stationary phase was evaluated in detail to determine its ion-exchange properties, separability, reproducibility, hydrophilicity, and the effect of column loading and pH on the separation and retention of proteins. It was found to have an ion-exchange chromatographic (IEC) retention mechanism. The dynamic protein loading capacity of the synthesized SAX packings for BSA was 27.4mg (.) g(-1). Four proteins were separated within 6.0 minutes using the synthesized WAX resin. The WAX resin was also used for the rapid separation and purification of recombinant human granulocyte colony stimulating factor (rhG-CFS) from the coarse extract solution with only one step. The purity of the purified rhG-CFS was more than 95%.
机译:基于8.0μm的单分散大孔聚(甲基丙烯酸缩水甘油酯-乙二甲基丙烯酸共乙酯)微珠(P-GMA / EDMA),通过新的化学改性方法合成了用于HPLC的新型亲水性弱阴离子交换(WAX)固定相方法。对固定相进行了详细评估,以确定其离子交换性能,可分离性,重现性,亲水性以及色谱柱上样量和pH对蛋白质分离和保留的影响。发现具有离子交换色谱(IEC)保留机制。合成的SAX填料对BSA的动态蛋白质负载能力为27.4mg(。)g(-1)。使用合成的WAX树脂在6.0分钟内分离了四种蛋白质。 WAX树脂还仅需一步即可用于从粗提液中快速分离和纯化重组人粒细胞集落刺激因子(rhG-CFS)。纯化的rhG-CFS的纯度大于95%。

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