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Preparation of strong anion-exchange chromatographic packings based on monodisperse polymeric beads and their application in the separation of biopolymers

机译:基于单分散聚合物珠的强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

A new hydrophilic strong anion-exchange (SAX) stationary phase for HPLC has been synthesized by chemical modification of macroporous 8.0-mu m monodisperse poly(glycidylmethacrylate-co-ethylenedimethacrylate) beads (P-GMA/EDMA). 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 highest dynamic protein loading capacity of the synthesized SAX packing for BSA was 22.6 mg g(-1). Five proteins were separated within 6.0 min using the synthesized SAX resin. The SAX resin was also used for rapid separation and purification of recombinant human stem cell factor (rhSCF) from a crude extract solution in only one step. The purity of the purified of rhSCF was > 92.4%.
机译:通过大孔8.0μm单分散聚(甲基丙烯酸缩水甘油酯-乙二甲基丙烯酸乙二酯)微珠(P-GMA / EDMA)的化学修饰,合成了一种新型的用于亲水性高效液相色谱的亲水性强阴离子交换(SAX)固定相。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的最高动态蛋白质负载量为22.6 mg g(-1)。使用合成的SAX树脂在6.0分钟内分离了5种蛋白质。 SAX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干细胞因子(rhSCF)。纯化的rhSCF的纯度> 92.4%。

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