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Anion exchange chromatography – Mass spectrometry for monitoring multiple quality attributes of erythropoietin biopharmaceuticals

  • Guusje van Schaick
  • , Christoph Gstöttner
  • , Alexander Büttner
  • , Dietmar Reusch
  • , M. Wuhrer
  • , Elena Domínguez-Vega*
  • *Corresponding author for this work

Research output: Contribution to Journal › Article › Academic › peer-review

Abstract

Assessment of critical quality attributes of the biopharmaceutical erythropoietin (EPO) prior to product release requires the use of several analytical methods. We developed an MS-compatible anion exchange (AEX) method for monitoring multiple quality attributes of EPO biopharmaceuticals. AEX was performed using a stationary phase with quaternary ammonium functional groups and a pH gradient for elution. Baseline separation of charge variants and high-quality MS data were achieved using 30 mM ammonium formate pH 5.5 and 30 mM formic acid pH 2.5 as mobile phases. In a single experiment, assessment of critical quality attributes, such as charge heterogeneity, sialic acid content and number of N-acetyllactosamine units, was possible while providing additional information on other modifications such as O-acetylation and deamidation. In addition, good repeatability and robustness for the relative areas of the individual glycoforms and average number of Neu5Ac per EPO molecule were observed. The results were comparable to common pharmacopeia and standard methods with the advantage of requiring fewer analytical methods and less sample treatment saving time and costs.
Original languageEnglish
Pages (from-to)166-172
Number of pages7
JournalAnalytica Chimica Acta
Volume1143
Early online date26 Nov 2020
DOIs
Publication statusPublished - 25 Jan 2021

Funding

This work was supported by the Netherlands Organization for Scientific Research NWO (SATIN project, Grant No. 731.017.202) and the European Union’s Horizon 2020 (Analytics for biologics project, Grant No. 765502).

FundersFunder number
Netherlands Organization for Scientific Research NWO731.017.202
Horizon 2020 Framework Programme
Horizon 2020765502

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