• SyncroPatch 384

    Next level versatility and flexibility
  • SyncroPatch 384

    True HTS and GigaOhm seals
  • SyncroPatch 384

    Your multi purpose instrument
  • SyncroPatch 384

    Powerful analysis software
  • SyncroPatch 384

    Assay flexibility via high tech
  • SyncroPatch 384

    Heating and cooling of solutions, cells and patch clamp sites

2020 - Reliable Identification of hERG Liability in Drug Discovery by Automated Patch Clamp

 icon sp96   SyncroPatch 384i (a predecessor model of SyncroPatch 384) and   icon pl   Patchliner poster, 64th Annual Meeting of the Biophysical Society   logo pdf   (1.3 MB)


The Comprehensive in Vitro Proarrhythmia Assay (CiPA) is focused on proarrhythmia to improve specificity compared to in vitro hERG and in vivo QT studies. Within this initiative, compounds representing high, intermediate, and low proarrhythmic risk categories were tested across multiple sites and automated patch clamp (APC) platforms. Resulting IC50 values varied between platforms, which could be due to non-specific binding of compounds in well-based platforms since they don’t maintain a constant flow of compound-containing solution to replenish losses to fluidics and well walls.
Here, we investigated non-specific binding using hydrophobic (“sticky”) compounds to assess the reliability of our experimental routine by analyzing IC50 values of CiPA compounds. We equipped a 384-well APC platform with a state-of-the-art liquid handling robot and used its serial dilution capability for compound preparation. Glass-coated compound plates were used to prevent absorption of hydrophobic compounds. After compound preparation, the user-unattended experiments were executed and IC50 values of the compounds were measured and compared to literature values.
“Sticky” compounds such as verapamil were applied either as a single concentration per recording well or cumulatively in 4 increasing concentrations. Incubation times were varied. For example, IC50 values of verapamil were 0.66 μM (CiPA step-ramp hERG protocol, 7-minute incubation time) and 0.60 μM (standard hERG protocol, 4-minute incubation time), respectively, and thus in good agreement with themselves and literature values. Incubation times below 4 minutes were too short to reach steady-state currents. Results of further compounds e.g. terfenadine, chlorpromazine, quinidine and clozapine will also be presented.
The 384-well APC system used in this study (SyncroPatch 384i) is well suited to perform safety pharmacological studies within the guidelines of the CiPA initiative. Caution has to be taken on the handling and storage conditions of the compounds, as well as exposure times of the compounds during the measurement.

Back to Overview

We use cookies on our website. Some of them are essential for the operation of the site, while others help us to improve this site and the user experience (tracking cookies). You can decide for yourself whether you want to allow cookies or not. Please note that if you reject them, you may not be able to use all the functionalities of the site.