Development of a 3-step straight-through purification strategy combining membrane adsorbers and resins.

Biotechnol Prog

Federal University of Rio de Janeiro (UFRJ), COPPE, Chemical Engineering Program, Cell Culture Engineering Laboratory, Ilha do Fundao, Rio de Janeiro, 21941-972, Brazil.

Published: July 2017

AI Article Synopsis

  • The push for cost-effective biopharmaceutical production is leading to innovative techniques like straight-through processing (STP), which aims to purify compounds with minimal delays.
  • Researchers formulated and evaluated six different 3-step STP methods, using various purification techniques to isolate a complex glycoprotein from cell culture.
  • The most successful approach combined cation exchange, hydrophobic interaction, and affinity chromatography, achieving up to 88% recovery and effectively removing impurities, ultimately showcasing STP's potential for advanced biopharmaceutical manufacturing.

Article Abstract

The pressures to efficiently produce complex biopharmaceuticals at reduced costs are driving the development of novel techniques, such as in downstream processing with straight-through processing (STP). This method involves directly and sequentially purifying a particular target with minimal holding steps. This work developed and compared six different 3-step STP strategies, combining membrane adsorbers, monoliths, and resins, to purify a large, complex, and labile glycoprotein from Chinese hamster ovary cell culture supernatant. The best performing pathway was cation exchange chromatography to hydrophobic interaction chromatography to affinity chromatography with an overall product recovery of up to 88% across the process and significant clearance of DNA and protein impurities. This work establishes a platform and considerations for the development of STP of biopharmaceutical products and highlights its suitability for integration with single-use technologies and continuous production methods. © 2017 American Institute of Chemical Engineers Biotechnol. Prog., 33:931-940, 2017.

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Source
http://dx.doi.org/10.1002/btpr.2501DOI Listing

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