Construction of Discrimination Models of Cationic Drugs for Phospholipidosis Induction Potential by Using Interaction Data with Immobilized Artificial Membrane as Well as Physicochemical Properties-Reference-Cited by-同舟云学术

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Construction of Discrimination Models of Cationic Drugs for Phospholipidosis Induction Potential by Using Interaction Data with Immobilized Artificial Membrane as Well as Physicochemical Properties

Published:2024-08 Issue:8 Volume:113 Page:2625-2632
ISSN:0022-3549
Container-title:Journal of Pharmaceutical Sciences
language:en
Short-container-title:Journal of Pharmaceutical Sciences

Author:

Iwakuma Yoshie,Kuroda Yukihiro

Publisher

Elsevier BV

Reference27 articles.

1. Cationic amphiphilic drugs and phospholipid storage disorder;Kodavanti;Pharmacol Rev,1990

2. Bis(monoacylglycerol)phosphate as a non–invasive biomarker to monitor the onset and time–course of phospholipidosis with drug–induced toxicities;Tengstrand;Expert Opin Drug Metab Toxicol,2010

3. Drug–induced phospholipidosis confounds drug repurposing for SARS–CoV–2;Tummino;Science,2021

4. Phospholipidosis effect of drugs by adsorption into lipid monolayers;Ceccarelli;Colloids Surf B Biointerfaces,2015

5. Use of physicochemical calculation of pKa and ClogP to predict phospholipidosis–inducing potential: a case study with structurally related piperazines;Ploemen;Exp Toxicol Pathol,2004

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