A physiologically based pharmacokinetic model for open acid and lactone forms of atorvastatin and metabolites to assess the drug-gene interaction with SLCO1B1 polymorphisms-Reference-Cited by-同舟云学术

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A physiologically based pharmacokinetic model for open acid and lactone forms of atorvastatin and metabolites to assess the drug-gene interaction with SLCO1B1 polymorphisms

Published:2022-12 Issue: Volume:156 Page:113914
ISSN:0753-3322
Container-title:Biomedicine & Pharmacotherapy
language:en
Short-container-title:Biomedicine & Pharmacotherapy

Author:

Reig-López Javier,Merino-Sanjuan Matilde,García-Arieta Alfredo,Mangas-Sanjuán Victor

Publisher

Elsevier BV

Subject

Pharmacology,General Medicine

Reference50 articles.

1. Atorvastatin population pharmacokinetics in a real‐life setting: Influence of genetic polymorphisms and association with clinical response;Stillemans;Clin. Transl. Sci.,2021

2. Michael Schachter. Chemical, pharmacokinetic and pharmacodynamic properties of statins: an update. https://doi.org/10.1111/j.1472–8206.2004.00299.x.

3. Atorvastatin: an updated review of its pharmacological properties and use in dyslipidaemia;Malhotra;Drugs,2001

4. The pharmacology of statins;Sirtori;Pharmacol. Res.,2014

5. Atorvastatin: pharmacological characteristics and lipid-lowering effects;Poli;Drugs,2007

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