| Literature DB >> 33384114 |
Guusje van Schaick1, Christoph Gstöttner1, Alexander Büttner2, Dietmar Reusch2, Manfred Wuhrer1, Elena Domínguez-Vega3.
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.Entities:
Keywords: Anion exchange chromatography; Biopharmaceuticals; Critical quality attributes; Erythropoietin; High resolution mass spectrometry; Multiple attribute method
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Year: 2020 PMID: 33384114 DOI: 10.1016/j.aca.2020.11.027
Source DB: PubMed Journal: Anal Chim Acta ISSN: 0003-2670 Impact factor: 6.558