The identification and chromatographic separation of a new highly analogous impurity of the active pharmaceutical ingredient icatibant.
Chromatography
Firazyr®
Forced degradation
HOE 140
Icatibant
Isomerization
Peptidomimetic drugs
Journal
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences
ISSN: 1879-0720
Titre abrégé: Eur J Pharm Sci
Pays: Netherlands
ID NLM: 9317982
Informations de publication
Date de publication:
30 Apr 2019
30 Apr 2019
Historique:
received:
01
02
2019
revised:
28
02
2019
accepted:
03
03
2019
pubmed:
9
3
2019
medline:
25
7
2019
entrez:
9
3
2019
Statut:
ppublish
Résumé
Icatibant is a peptidomimetic drug serving as a bradykinin-receptor antagonist and is approved in Europe and the United States for the treatment of hereditary angioedema attacks. We have detected an impurity with a high structural similarity to icatibant in pharmaceutical dosage forms using an optimized chromatographic method based on reversed phase high performance liquid chromatography with UV detection. The abundance of the impurity was around 1% relative to the icatibant peak following storage at room temperature for 1 month, and raised up to ~16% upon temperature stressing at 100 °C. The impurity was isolated by fraction collection and further purified by solid phase extraction for structural identification. NMR and high resolution mass spectrometric analyses revealed that this impurity results from isomerization in the N-terminal single amino acid residue. The new impurity may warrant particular attention due to its exceptional similarity to the active ingredient icatibant.
Identifiants
pubmed: 30849486
pii: S0928-0987(19)30100-9
doi: 10.1016/j.ejps.2019.03.003
pii:
doi:
Substances chimiques
Bradykinin B2 Receptor Antagonists
0
icatibant
7PG89G35Q7
Bradykinin
S8TIM42R2W
Types de publication
Journal Article
Langues
eng
Pagination
121-124Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.