对非活化SARS-CoV-2疫苗和不同染色学介质净化效应下游生产过程的稳定性验证的评估
Jia-Hui Pang1,2, Chang-Fu Guo2, Peng-Liang Hao2
1National Engineering Technology Research Center for Combined Vaccines, Wuhan 430207, China.
Vaccines
|January 22, 2024
概括
目前WIBP-CorV疫苗生产的下游流程是稳健的,可以适应各种批次和染色学介质. 这确保了无活化SARS-CoV-2疫苗的高效净化.
科学领域:
- 生物技术是生物技术.
- 疫苗开发 疫苗开发
- 下游加工 下游加工
背景情况:
- 大规模的疫苗生产需要强大的,高效的和具有成本效益的下游加工.
- 优化净化方法对于确保疫苗质量和产量至关重要.
研究的目的:
- 评估WIBP-CorV疫苗生产现有的下游流程的稳定性.
- 评估不同染色体介质对疫苗净化疗效的影响.
主要方法:
- 处理了三批COVID-19 Omicron BA.1菌株的液溶性缩溶液.
- 测试了四种凝过和四种离子交换色谱介质.
- 通过测量总蛋白质,抗原含量和残留杂质 (DNA,蛋白质,BSA) 来评估疫苗的质量.
主要成果:
- 在抗原回收,Vero宿主细胞蛋白,Vero DNA或BSA残留量之间没有发现显著差异.
- 在抗原含量方面发现了显著的差异 (p < 0.001).
- 测试的染色体介质显示了可比的净化性能.
结论:
- 目前的下游流程对WIBP-CorV疫苗生产具有显著的稳定性.
- 该过程可以适应水溶性缩溶液和色谱介质的变化.
- 这项研究为净化其他病毒疫苗提供了有价值的模板.
相关概念视频
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