Early assessment of proarrhythmic risk of drugs using the in vitro data and single-cell-based in silico models: proof of concept. (12th February 2017)

• Record Type: Journal Article
• Authors: Abbasi, Mitra; Small, Ben G.; Patel, Nikunjkumar; Jamei, Masoud; Polak, Sebastian
• Is Part Of: Toxicology mechanisms and methods. Volume 27:Number 2(2017)
• Page Start: 88
• Page End: 99
• Publication Date: 2017-02-12
• Subjects: In silico assessment -- in silico screening -- drug safety -- cardiac arrhythmias -- QT prolongation -- early afterdepolarization; Analytical toxicology -- Periodicals; Toxicology -- Periodicals; Toxicology -- Methodology -- Periodicals; 615.907
• DOI: 10.1080/15376516.2016.1256460
• Languages: English
• ISSNs: 1537-6516

Abstract

Abstract: Background and purpose: To determine the predictive performance of in silico models using drug-specific preclinical cardiac electrophysiology data to investigate drug-induced arrhythmia risk (e.g. Torsade de pointes (TdP)) in virtual human subjects. Experimental approach: To assess drug proarrhythmic risk, we used a set of in vitro electrophysiological measurements describing ion channel inhibition triggered by the investigated drugs. The Cardiac Safety Simulator version 2.0 (CSS; Simcyp, Sheffield, UK) platform was used to simulate human left ventricular cardiac myocyte action potential models. Results: This study shows the impact of drug concentration changes on particular ionic currents by using available experimental data. The simulation results display safety threshold according to drug concentration threshold and log (threshold concentration/ effective therapeutic plasma concentration (ETPC)). Conclusion and implications: We reproduced the underlying biophysical characteristics of cardiac cells resulted in effects of drugs associated with cardiac arrhythmias (action potential duration (APD) and QT prolongation and TdP) which were observed in published 3D simulations, yet with much less computational burden.