4.7 Article

Structurally related peptide impurity identification and accurate quantification for synthetic oxytocin by liquid chromatography-high-resolution mass spectrometry

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 413, Issue 7, Pages 1861-1870

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-021-03154-5

Keywords

Oxytocin; Synthetic peptide; Impurity; Liquid chromatography; High-resolution mass spectrometry

Funding

  1. National Key R&D Program of China [2017YFF0205403]

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Oxytocin is a crucial peptide used for labor induction and postpartum bleeding control, but also shows potential as a biomarker for emotions and cancer diagnosis. Accurate purity characterization through various methods is essential, considering the unique analytical challenge posed by the presence of disulfide bonds in Oxytocin. Newly developed LC-hrMS method has been effective in identifying and quantifying structurally related impurities in synthetic OXT materials.
Oxytocin (OXT) is an important peptide that is mainly used as a therapeutic drug to induce labor or strengthen uterine contractions, or to control bleeding after childbirth. OXT has also been reported as a biomarker linked to emotion, and as a potential biomarker for cancer diagnosis. The accurate purity characterization of OXT calibrators is critical for quality control of pharmaceuticals and the development of reference measurement systems for this analyte in laboratory medicine. OXT possesses the particular analytical measurement challenge of a disulfide bond. Accurate value assignment of the purity of oxytocin calibrators can be carried out by applying the mass balance approach or alternative approaches such as amino acid analysis, quantitative nuclear magnetic resonance spectrometry, and nitrogen determination. In order to avoid biases, all these approaches require a correction for structurally related peptide impurities. Structurally related peptide impurities present in a synthetic OXT material have been identified and quantified by a newly developed and in-house-validated liquid chromatography-high-resolution mass spectrometry (LC-hrMS) method. This method was adopted for the measurement of the study material used for an international comparison evaluating the competencies of laboratories to perform peptide characterization. Eighteen structurally related impurities were identified, confirmed, and accurately quantified in the OXT study material by using LC-hrMS. The study material contained a total mass fraction of 31.1 mg/g structurally related OXT impurities with an associated expanded uncertainty of 1.7 mg/g.

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