4.5 Article Proceedings Paper

A fast and efficient purification platform for cell-based influenza viruses by flow-through chromatography

期刊

VACCINE
卷 36, 期 22, 页码 3146-3152

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2017.03.016

关键词

Influenza vaccine; Cell culture; Purification process; Flow-through chromatography

资金

  1. Ministry of Science and Technology, R.O.C. [102-2622-B-400-001-CC2, 103-2622-B-400-001-CC2, 102-2321-B-400-022]
  2. National Health Research Institutes, R.O.C. [IV-105-PP-25]

向作者/读者索取更多资源

Since newly emerging influenza viruses with pandemic potentials occurred in recent years, the demand for producing pandemic influenza vaccines for human use is high. For the development of a quick and efficient vaccine production, we proposed an efficient purification platform from the harvest to the purified bulk for the cell-based influenza vaccine production. This platform based on flow-through chromatography and filtration steps and the process only involves a few purification steps, including depth filtration, inactivation by formaldehyde, microfiltration, ultrafiltration, anion-exchange and ligand-core chromatography and sterile filtration. In addition, in the proposed chromatography steps, no virus capture steps were employed, and the purification results were not affected by the virus strain variation, host cells and culturing systems. The results from different virus strains which produced by Vero or MDCK cells in different culturing systems also obtained 33-46% HA recovery yields by this platform. The overall removal rates of the protein and DNA concentration in the purified bulk were over 96.1% and 99.7%, respectively. The low residual cellular DNA concentrations were obtained ranged from 30 to 130 pg per human dose (15 mu g/dose). All influenza H5N1 purified bulks met the regulatory requirements for human vaccine use. (C) 2017 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据