Effects of wet granulation process variables on the quantitative assay model of transmission Raman spectroscopy for pharmaceutical tablets.

Content uniformity In-process control Process analytical technology Tablet formulation Transmission Raman spectroscopy Wet granulation

Journal

European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V
ISSN: 1873-3441
Titre abrégé: Eur J Pharm Biopharm
Pays: Netherlands
ID NLM: 9109778

Informations de publication

Date de publication:
Oct 2023
Historique:
received: 03 08 2023
revised: 11 09 2023
accepted: 12 09 2023
medline: 2 10 2023
pubmed: 16 9 2023
entrez: 15 9 2023
Statut: ppublish

Résumé

Transmission Raman spectroscopy (TRS) is a process analytical technology tool for nondestructive analysis of drug content in tablets. Although wet granulation is the most used tablet manufacturing method, most TRS studies have focused on tablets manufactured via direct compression. The effects of upstream process parameter variations, such as granulation, on the prediction performance of TRS quantitative models are unknown. We evaluated the effects of process parameter variations during granulation on the prediction performance of the TRS quantitative model. Tablets with a drug concentration of 1%w/w were used. We developed PLS calibration models for the drug concentration range of 70-130% label claims. Subsequently, we predicted the drug content of the tablets with different granulation parameters. The results of our study demonstrate that the variation in the predicted recovery due to the variation in granulation parameters was practically acceptable. The calibration model showed a good prediction performance for tablets manufactured at different granulation scales and thicknesses. Therefore, we conclude that TRS quantitative models are robust to variations in upstream processes, such as granulation and downstream variations in tableting parameters. These results suggest that TRS is a versatile non-destructive quantitative analysis method that can be applied in tablet manufacturing.

Identifiants

pubmed: 37714414
pii: S0939-6411(23)00242-4
doi: 10.1016/j.ejpb.2023.09.009
pii:
doi:

Substances chimiques

Tablets 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

276-289

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

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

Ryo Ohashi (R)

Department of Molecular Pharmaceutics, Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo 204-8588 Japan; Formulation R&D Laboratory, R&D Division, SHIONOGI & CO., LTD., Hyogo 660-0813, Japan. Electronic address: ryo.ohashi@shionogi.co.jp.

Tatsuo Koide (T)

Division of Drugs, National Institute of Health Sciences, Tonomachi, Kawasaki-ku, Kawasaki 210-9501, Japan.

Toshiro Fukami (T)

Department of Molecular Pharmaceutics, Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo 204-8588 Japan.

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Classifications MeSH