EMD Millipore, Purification Product Development, Bedford, MA 01730, USA.
J Chromatogr A. 2011 Jul 1;1218(26):3973-81. doi: 10.1016/j.chroma.2011.04.086. Epub 2011 May 6.
A method for flow-through purification of viruses and virus like nano-particles using a combination of binding and size-exclusion chromatography was developed. This technique relies on minimizing the external surface area per unit volume available for virus binding by increasing the mean diameter of the beads used in the column. At the same time the impurity binding capacity of the column is maximized by utilizing beads with multiple functionalities of the optimum size. Purification of different types of viruses and virus-like-particles could be achieved using this technique. Flow-through purification of influenza virus using this technique yielded virus recoveries greater than 70-80% coupled with impurity removal greater than 80%. Finally an approach to optimize and facilitate process development using this technology is presented. Since the impurity binding occurs via a non-specific mechanism and virus recovery is achieved through reduced surface area, the technique is not limited to specific types of viruses and offers the potential as a universal purification tool.
开发了一种使用结合和排阻色谱相结合的方法,用于病毒和类似病毒的纳米颗粒的流穿式纯化。该技术通过增加柱中使用的珠子的平均直径,从而最小化单位体积可用于病毒结合的外表面面积。同时,通过利用具有最佳尺寸的多功能珠子,最大化柱的杂质结合能力。可以使用该技术纯化不同类型的病毒和类似病毒的颗粒。使用该技术对流感病毒进行的流穿式纯化,病毒回收率大于 70-80%,同时杂质去除率大于 80%。最后提出了一种优化和简化该技术工艺开发的方法。由于杂质结合是通过非特异性机制发生的,并且通过减少表面积来实现病毒回收,因此该技术不仅限于特定类型的病毒,并且作为通用的纯化工具具有潜力。