• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

从灌注细胞培养生物反应器中回收高纯度生物制药产品。

The recovery of highly purified biopharmaceuticals from perfusion cell culture bioreactors.

作者信息

Prior C P, Doyle K R, Duffy S A, Hope J A, Moellering B J, Prior G M, Scott R W, Tolbert W R

出版信息

J Parenter Sci Technol. 1989 Jan-Feb;43(1):15-23.

PMID:2926601
Abstract

The impact of continuous perfusion cell culture technology on production of one and two chain human rtPA, as well as monoclonal IgG and IgM, will be reviewed. Perfusion as compared to batch systems improve the quality of the product in the conditioned media in terms of biological activity and structural integrity. This significantly increases downstream recovery and daily production output of final purified material. These findings are a consequence of the ability of perfusion technology to 1) maintain cells intact at high cell density; 2) effectively reduce serum content to approximate serum free conditions; and 3) minimize residency time of labile product within the 37 degrees C environment of the bioreactor.

摘要

本文将综述连续灌注细胞培养技术对单链和双链人重组组织型纤溶酶原激活剂(rtPA)以及单克隆IgG和IgM生产的影响。与分批培养系统相比,灌注培养在生物活性和结构完整性方面提高了条件培养基中产品的质量。这显著提高了下游回收效率和最终纯化材料的日产量。这些发现是由于灌注技术能够:1)在高细胞密度下保持细胞完整;2)有效降低血清含量至接近无血清条件;3)将不稳定产品在生物反应器37摄氏度环境中的停留时间降至最低。

相似文献

1
The recovery of highly purified biopharmaceuticals from perfusion cell culture bioreactors.从灌注细胞培养生物反应器中回收高纯度生物制药产品。
J Parenter Sci Technol. 1989 Jan-Feb;43(1):15-23.
2
Conversion of a CHO cell culture process from perfusion to fed-batch technology without altering product quality.在不改变产品质量的情况下,将CHO细胞培养工艺从灌注技术转换为补料分批技术。
J Biotechnol. 2006 May 3;123(1):106-16. doi: 10.1016/j.jbiotec.2005.10.013. Epub 2005 Dec 1.
3
Animal cell cultures: recent achievements and perspectives in the production of biopharmaceuticals.动物细胞培养:生物制药生产中的最新成就与展望
Appl Microbiol Biotechnol. 2005 Aug;68(3):283-91. doi: 10.1007/s00253-005-1980-8. Epub 2005 Apr 16.
4
Bioreactor systems for the production of biopharmaceuticals from animal cells.用于从动物细胞生产生物制药的生物反应器系统。
Biotechnol Appl Biochem. 2006 Jul;45(Pt 1):1-12. doi: 10.1042/BA20050233.
5
Manufacture of pharmaceutical proteins from hybridomas and other cell substrates.利用杂交瘤和其他细胞底物生产药用蛋白质。
Dev Biol Stand. 1989;70:49-56.
6
Continuous downstream processing of biopharmaceuticals.生物制药的连续下游处理。
Trends Biotechnol. 2013 Aug;31(8):479-92. doi: 10.1016/j.tibtech.2013.05.011. Epub 2013 Jul 10.
7
High-level production of a monoclonal antibody in murine myeloma cells by perfusion culture using a gravity settler.使用重力沉降器通过灌注培养在鼠骨髓瘤细胞中高效生产单克隆抗体。
Biotechnol Prog. 2007 Jan-Feb;23(1):225-31. doi: 10.1021/bp060231v.
8
Large scale animal cell cultivation for production of cellular biologicals.用于生产细胞生物制品的大规模动物细胞培养。
Dev Biol Stand. 1985;60:229-36.
9
Achievement of high cell density and high antibody productivity by a controlled-fed perfusion bioreactor process.通过控制补料灌注生物反应器工艺实现高细胞密度和高抗体生产率
Biotechnol Bioeng. 2000 Jul 5;69(1):74-82.
10
High-titer adenovirus vector production in 293S cell perfusion culture.在293S细胞灌注培养中生产高滴度腺病毒载体
Biotechnol Prog. 2004 May-Jun;20(3):858-63. doi: 10.1021/bp034237l.

引用本文的文献

1
Downstream processing of insect cell cultures.昆虫细胞培养的下游处理
Cytotechnology. 1996 Jan;20(1-3):239-57. doi: 10.1007/BF00350404.
2
Repeated hybridoma batch culture with cell recycle.采用细胞循环的重复杂交瘤分批培养。
Cytotechnology. 1993;13(1):51-3. doi: 10.1007/BF00749975.
3
Nutrient optimization for high density biological production applications.用于高密度生物生产应用的营养优化。
Cytotechnology. 1991 Jan;5(1):15-30. doi: 10.1007/BF00365531.