Flow-Through Purification of Viruses- A Novel Approach to Vaccine Purification

Ganesh Iyer, Senthilkumar Ramaswamy, Kwok-Shun Cheng, Nakry Sisowath, Ushma Mehta, Anne Leahy, Franklin Chung, Damon Asher
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引用次数: 16

Abstract

A two step flow-through chromatography process is proposed as an universal approach to purify viruses. A resin column with reduced surface area was developed for the first step to remove bulk of the host cell protein (HCP) from a viral feed stream while allowing most of the virus to flow-through. For the second step a chromatographic separations strategy using a primary amine membrane adsorber and multivalent ions in the mobile phase was developed. This enabled selective binding of host cell DNA (hcDNA) to the membrane and complete recovery of virus in the flow-through mode. The techniques were evaluated using cell culture grown influenza virus and bacteriophage feed streams. Virus recoveries of >70-80% and 100% were achieved for the column and membrane approaches respectively. The column cleared > 80% of the HCP and the membrane adsorber reduced whole hcDNA levels to <10 ng.

病毒的流动纯化——一种新的疫苗纯化方法
提出了一种两步流式色谱法作为纯化病毒的通用方法。第一步是开发一种表面积减小的树脂柱,用于从病毒饲料流中去除大部分宿主细胞蛋白(HCP),同时允许大多数病毒流过。第二步,建立了伯胺膜吸附剂和流动相多价离子的色谱分离策略。这使得宿主细胞DNA (hcDNA)选择性地结合到膜上,并在流动模式下完全恢复病毒。使用细胞培养的流感病毒和噬菌体饲料流对这些技术进行了评估。柱法和膜法的病毒回收率分别为70-80%和100%。列被清除了>80%的HCP和膜吸附剂将整个hcDNA水平降低至10 ng。
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