N-Nitrosamine Formation in Pharmaceutical Solid Drug Products: Experimental Observations.

Carcinogenic impurities Drug product Formulations Impurities Mutagenic impurities N-nitrosamines Nitrosamines Pharmaceuticals

Journal

Journal of pharmaceutical sciences
ISSN: 1520-6017
Titre abrégé: J Pharm Sci
Pays: United States
ID NLM: 2985195R

Informations de publication

Date de publication:
05 2023
Historique:
received: 09 12 2022
revised: 25 01 2023
accepted: 26 01 2023
medline: 24 4 2023
pubmed: 4 2 2023
entrez: 3 2 2023
Statut: ppublish

Résumé

The potential presence of N-nitrosamines in medicinal products has become a matter of concern for health authorities and pharmaceutical companies. However, very little information is available in published literature on N-nitrosamine formation within pharmaceutical drug products. In response, experiments were undertaken to test if secondary and tertiary amines present in solid drug products could undergo nitrosation due to the presence of nitrite in the excipients used in the manufacture of the drug product. This work focused on solid dosage forms exploring several model amines of varying chemical structure, solubility and pKa which were formulated using common excipients with and without added nitrite. Monitoring the formation of the N-nitrosamines after processing and upon stressed stability conditions showed that N-nitrosamine formation can occur in solid drug product formulations. The results show that the rate and extent of N-nitrosamine formation depend upon the solubility of the amine, level of nitrite, expected local acidity in water layers within the drug product and mode of processing. Our findings agree with the rank order of dosage form risk from the published EFPIA workflows for quality risk management of N-nitrosamine risks in medicines (EFPIA, 2022): amorphous > wet granulation > direct compression > dry blends. In all cases the level of N-nitrosamine formation in solid dosage forms plateaued at a level that was significantly lower than the maximum theoretical yield based on the level of nitrite present. Trace secondary amine impurities were shown to be a significantly lower risk relative to cases containing a secondary amine present at drug substance levels. A comparison of secondary and simple tertiary alkylamine reactivity showed the tertiary amine to be significantly less reactive with nitrite.

Identifiants

pubmed: 36736774
pii: S0022-3549(23)00028-X
doi: 10.1016/j.xphs.2023.01.027
pii:
doi:

Substances chimiques

Nitrosamines 0
Nitrites 0
Excipients 0
Amines 0
Water 059QF0KO0R

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1255-1267

Informations de copyright

Copyright © 2023. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Justin Moser (J)

Pharmaceutical Sciences & Clinical Supplies, Merck & Co., Inc., West Point, PA, United States. Electronic address: justin_moser@merck.com.

Ian W Ashworth (IW)

Chemical Development, Pharmaceutical Technology & Development, Operations, AstraZeneca, Macclesfield, United Kingdom.

Laurence Harris (L)

Pfizer R&D UK Limited, Discovery Park, Ramsgate Road, Sandwich, CT13 9NJ, United Kingdom.

Michael C Hillier (MC)

Operations Science & Technology, API Products, Abbvie Inc. North Chicago, IL, United States.

Kausik K Nanda (KK)

Discovery Pharmaceutical Sciences, Merck & Co., Inc., West Point, PA, United States.

Garry Scrivens (G)

Pfizer R&D UK Limited, Discovery Park, Ramsgate Road, Sandwich, CT13 9NJ, United Kingdom.

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Classifications MeSH