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Method development for mono- and disaccharides monitoring in cell culture medium by capillary and microchip electrophoresis

  • Debbie van der Burg
  • , Leila Josefsson
  • , Saara Mikkonen
  • , Véronique Chotteau
  • , Åsa Emmer
  • , Hermann Wätzig
  • , Cari E Sänger-van de Griend

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

The rapidly growing, competitive biopharmaceutical market requires tight bioprocess monitoring. An integrated, automated platform for the routine online/at-line monitoring of key factors in the cell culture medium could greatly improve process monitoring. Mono- and disaccharides, as the main energy and carbon source, are one of these key factors. A CE-LIF method was developed for the analysis of several mono- and disaccharides, considering requirements and restrictions for analysis in an integrated, automated monitoring platform, such as the possibility for miniaturization to microchip electrophoresis. Analysis was performed after fluorescent derivatization with 8-aminopyrene-1,3,6-trisulfonic acid. The derivatisation reaction and the separation BGE were optimized using design of experiments. The developed method is applicable to the complex matrix of cell culture medium and proved transferable to microchip electrophoresis.

Original languageEnglish
Pages (from-to)922-929
Number of pages8
JournalElectrophoresis
Volume43
Issue number9-10
Early online date12 Sept 2021
DOIs
Publication statusPublished - May 2022

Bibliographical note

Special Issue: Electromigration and liquid chromatography techniques in pharmaceutical analysis 2022.

© 2021 Kantisto BV. Electrophoresis published by Wiley-VCH GmbH.

Funding

This research was part of the iConsensus project, a Joint Undertaking of the Innovative Medicines Initiative 2 (grant agreement No 777397), which receives support from the European Union Horizon 2020research and innovation programme and EFPIA partners Sanofi, GSK, Bayer, Rentschler Biopharma, UCB, Byondis, and Pfizer. Meeri Mäkinen and Atefeh Shokri (Department of Industrial Biotechnology, KTH Royal Institute of Technology) are acknowledged for the cell culture medium samples. The authors gratefully acknowledge Byondis for use of their facilities, Agilent Technologies Netherlands for providing CE instrumentation, and Micronit B.V. for facilitating ME measurements. (). This research was part of the iConsensus project, a Joint Undertaking of the Innovative Medicines Initiative 2 grant agreement No 777397 , which receives support from the European Union Horizon 2020 research and innovation programme and EFPIA partners Sanofi, GSK, Bayer, Rentschler Biopharma, UCB, Byondis, and Pfizer. Meeri Mäkinen and Atefeh Shokri (Department of Industrial Biotechnology, KTH Royal Institute of Technology) are acknowledged for the cell culture medium samples. The authors gratefully acknowledge Byondis for use of their facilities, Agilent Technologies Netherlands for providing CE instrumentation, and Micronit B.V. for facilitating ME measurements

FundersFunder number
European Union Horizon 2020research
Kungliga Tekniska Högskolan
Bayer
UCB
Rentschler Biopharma
GlaxoSmithKline
Department of Industrial Biotechnology
Sanofi
Innovative Medicines Initiative
Pfizer
Horizon 2020
Horizon 2020 Framework Programme777397

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 7 - Affordable and Clean Energy
      SDG 7 Affordable and Clean Energy

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