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相关概念视频

Upstream Processing01:27

Upstream Processing

Upstream processing represents a critical phase in biomanufacturing, wherein biological systems such as microorganisms, mammalian cells, or insect cells are cultivated to produce therapeutic proteins, vaccines, enzymes, or other biologically derived products. This phase encompasses all steps from the selection and genetic manipulation of the production organism to the cultivation of cells in bioreactors under tightly controlled environmental conditions.Host Selection and Genetic OptimizationThe...
Production of Pharmaceuticals01:30

Production of Pharmaceuticals

Industrial insulin production uses genetically engineered E. coli expressing a proinsulin gene controlled by a tryptophan promoter and containing a methionine linker for later cleavage. The cells also carry ampicillin resistance for selective growth. Seed cultures are stored at −80 °C and production begins by thawing a small amount to inoculate starter cultures, which are progressively scaled to a 50,000-L bioreactor. In the bioreactor, E. coli grow in nutrient-rich media under sterile, tightly...
Vaccine Production01:23

Vaccine Production

Vaccine production involves a sequence of upstream and downstream processes to generate a safe and effective immunological product. It begins with cultivating microorganisms, such as viruses or bacteria, to obtain antigenic material. For viral vaccines, mammalian host cells are grown in bioreactors and subsequently infected with the target virus. The virus replicates within the host cells, which are lysed to release viral particles. This lysate is then clarified through filtration or...
Downstream Processing01:29

Downstream Processing

Downstream processing begins once fermentation is complete and involves a series of steps to recover and purify products such as acids, vitamins, antibiotics, or proteins.Cell HarvestingFor example, for intracellular protein-based products, the first step is harvesting the cells. This is typically achieved using centrifugation or filtration to separate the cells from the liquid phase.Cell Disruption for Intracellular ProductsIf the target product is intracellular, the harvested cells must be...

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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.

European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V
|August 7, 2024
PubMed
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.

关键词:
细菌菌体是一种细菌体.菌体活性药物成分的药物成分.菌酸盐杂质 菌酸盐杂质菌体净化 菌体净化过程开发过程的合理化.分离单元的运作情况.

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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.