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菌体活性药物成分的净化过程的合理化
B Lapras1, C Marchand2, C Merienne2
1Hospices Civils de Lyon, Edouard Herriot Hospital, Pharmacy Department, FRIPHARM®, F-69437 Lyon, France; Claude Bernard Lyon 1 University, French National Centre for Scientific Research (CNRS), Institut de Biologie et de Chimie des Protéines (IBCP), Tissue Biology and Therapeutic Engineering Laboratory (LBTI), UMR 5305, F-69007 Lyon, France.
概括
由于抗生素耐药性,菌体疗法正在复苏. 本综述详细介绍了细菌菌体 (菌体) 的四步净化过程,解决了杂质挑战,并使治疗用途的可扩展生产成为可能.
科学领域:
- 生物技术是生物技术.
- 生物工艺工程 生物工艺工程
- 微生物学 微生物学
背景情况:
- 菌体疗法是抗生素的潜在替代品,在净化和稳定方面面临着挑战.
- 抗生素耐药性的上升需要对菌体治疗产生新的兴趣和发展.
研究的目的:
- 审查菌体溶解物中常见的杂质.
- 介绍细菌菌体的四步净化过程.
- 为开发可扩展和可转移的菌体净化过程提出框架.
主要方法:
- 关于污染物,菌体相关和传播相关杂质的物理化学性质的讨论.
- 制定一个四个阶段的净化策略:澄清,捕获/缩,净化和抛光.
- 制定一个框架,考虑过程设计的可扩展性,可转移性和持续时间.
主要成果:
- 鉴定菌体溶解酸中的关键杂质和消除它们的策略.
- 一个针对细菌菌体量身定制的结构化四步净化过程.
- 一个框架来指导菌体净化过程的合理开发和验证.
结论:
- 分离技术的进步使得高效的菌体净化成为可能.
- 拟议的框架有助于选择和验证可扩展的菌体生产的单元操作.
- 这项工作通过解决关键的制造挑战来支持菌体治疗的复兴.
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