Prediction of combination effect of quinidine on the pharmacokinetics of tipepidine using a physiologically based pharmacokinetic model.

CYP2D6 Drug interaction Drug repositioning Physiologically based pharmacokinetic modelling Tipepidine

Journal

Xenobiotica; the fate of foreign compounds in biological systems
ISSN: 1366-5928
Titre abrégé: Xenobiotica
Pays: England
ID NLM: 1306665

Informations de publication

Date de publication:
09 Jan 2024
Historique:
medline: 9 1 2024
pubmed: 9 1 2024
entrez: 9 1 2024
Statut: aheadofprint

Résumé

Tipepidine, an antitussive drug, has been reported to have central pharmacological effects and can be expected to be safely repositioned as treatment for psychiatric disorders. Since tipepidine requires three doses per day, development of a once-daily medication would be highly beneficial. Previously, we reported that combination use with quinidine, a CYP2D6 inhibitor, prolongs the half-life of tipepidine in chimeric mice with humanized liver.In this study, to predict this combination effect in humans, a physiologically based pharmacokinetic (PBPK) model was developed, and quantitative simulation was conducted. The simulation results indicated that concomitant administration of tipepidine with quinidine increased the predicted

Identifiants

pubmed: 38193900
doi: 10.1080/00498254.2024.2304129
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-13

Auteurs

Shun Hayashi (S)

Preclinical Research Unit, Drug Research Division, Sumitomo Pharma Co., Ltd, Osaka, Japan.
Drug Metabolism and Toxicology, Faculty of Pharmaceutical Sciences, Kanazawa University, Kanazawa, Japan.

Hiroko Kawaguchi (H)

Preclinical Research Unit, Drug Research Division, Sumitomo Pharma Co., Ltd, Osaka, Japan.

Takao Watanabe (T)

Drug Research Division, Sumitomo Pharma Co., Ltd, Osaka, 554-0022, Japan.

Izuru Miyawaki (I)

Preclinical Research Unit, Drug Research Division, Sumitomo Pharma Co., Ltd, Osaka, Japan.

Tatsuki Fukami (T)

Drug Metabolism and Toxicology, Faculty of Pharmaceutical Sciences, Kanazawa University, Kanazawa, Japan.
WPI Nano Life Science Institute (WPI-NanoLSI), Kanazawa University, Kanazawa, Japan.

Miki Nakajima (M)

Drug Metabolism and Toxicology, Faculty of Pharmaceutical Sciences, Kanazawa University, Kanazawa, Japan.
WPI Nano Life Science Institute (WPI-NanoLSI), Kanazawa University, Kanazawa, Japan.

Classifications MeSH