核酸酶
溶解
色谱法
核酸
甲肝疫苗
酶
化学
甲型肝炎病毒
水解
下游加工
离子交换
生物化学
离子色谱法
乙型肝炎表面抗原
细胞培养
病毒
生物
乙型肝炎病毒
病毒学
离子
有机化学
遗传学
作者
A J Hagen,R A Aboud,P A DePhillips,Cynthia N. Oliver,C J Orella,Robert D. Sitrin
出处
期刊:PubMed
日期:1996-06-01
卷期号:23 (3): 209-15
被引量:14
摘要
The development of the purification process for VAQTA, which results in a highly purified inactivated hepatitis A vaccine, was driven by modifications in the cell-culture and harvest methods which permit hepatitis A virus propagation to support large-scale manufacture. The starting material for the purification was initially a concentrated cell pellet scraped from roller bottles. However, when the cell-culture method was scaled up to use high-surface-area Nunc cell factories or Costar cubes, the early steps in the process had to be modified to handle large volumes of dilute lysate. Membrane concentration was used at first, and a highly purified vaccine was prepared, but virus-poly(nucleic acid) complexes were formed, which reduced the yields in later processing steps. The introduction of a nuclease digestion immediately after harvest followed by capture chromatography on an anion-exchange column eliminated the formation of these complexes and resulted in more consistent performance and higher yields of downstream operations.
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