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Prediction of combination effect of quinidine on the pharmacokinetics of tipepidine using a physiologically based pharmacokinetic model.
Hayashi, Shun; Kawaguchi, Hiroko; Watanabe, Takao; Miyawaki, Izuru; Fukami, Tatsuki; Nakajima, Miki.
Afiliação
  • Hayashi S; Preclinical Research Unit, Drug Research Division, Sumitomo Pharma Co, Ltd, Japan.
  • Kawaguchi H; Drug Metabolism and Toxicology, Kanazawa University, Kanazawa, Japan.
  • Watanabe T; Preclinical Research Unit, Drug Research Division, Sumitomo Pharma Co, Ltd, Japan.
  • Miyawaki I; Drug Research Division, Sumitomo Pharma Co, Ltd, Japan.
  • Fukami T; Preclinical Research Unit, Drug Research Division, Sumitomo Pharma Co, Ltd, Japan.
  • Nakajima M; Drug Metabolism and Toxicology, Kanazawa University, Kanazawa, Japan.
Xenobiotica ; 54(3): 107-115, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38193900
ABSTRACT
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 humanised 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 Cmax, AUC, and t1/2 of tipepidine in the Japanese population by 3.4-, 6.6-, and 2.4-fold, respectively.Furthermore, to compare with another approach that aims to prolong the half-life, the PK profile of tipepidine administered in hypothetical extended-release form was simulated. Extended-release form was predicted to be more influenced by CYP2D6 genotype than combination with quinidine, and the predicted plasma exposure was markedly increased in poor metabolizers, potentially leading to adverse effects.In conclusion, quantitative simulation using the PBPK model suggests the feasibility of the safe repositioning of tipepidine as a once-daily medication in combination with quinidine.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Piperidinas / Quinidina Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Piperidinas / Quinidina Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article