Detect Neurotoxic Risk Early. Protect CNS Development.
Our neurotoxicity services are designed to identify functional effects on neurons and neuronal networks, supporting safer and more efficient CNS and non-CNS drug development.
Our neurotoxicity services are supported by validated electrophysiology platforms widely used in neuroscience research.
Patchliner — Nanion Technologies
Automated patch clamp for neuronal ion channel studies.
The Patchliner enables functional assessment of ion channel activity in neuronal systems. It provides automated whole-cell recordings from neurons and neuronal cell lines, allowing for the evaluation of compound effects on neuronal excitability and ion channel function.
Best suited for: Neuronal ion channel screening, medium-throughput neurotoxicity assessment, functional profiling
NANION TECHNOLOGIES MEDIUM THROUGHPUT
Manual Patch Clamp
Detailed characterization of neuronal excitability and firing properties.
Conventional whole-cell electrophysiology systems provide high-resolution recordings of neuronal activity. This gold-standard approach allows for detailed analysis of action potential properties, firing patterns, and synaptic responses in individual neurons.
Best suited for: Detailed neuronal characterization, action potential analysis, synaptic transmission studies
GOLD STANDARD HIGH RESOLUTION
MEA Systems — Multi Channel Systems (MCS)
Long-term, non-invasive recordings of neuronal network activity.
Multi-Electrode Array (MEA) technology enables simultaneous recording from multiple electrodes in neuronal networks over extended periods. This approach captures emergent network properties, including synchronization, burst dynamics, and functional connectivity that cannot be observed at the single-cell level.
Best suited for: Network-level neurotoxicity assessment, seizure liability detection, chronic exposure studies
MCS NETWORK PHYSIOLOGY
Definition of neurotoxicity endpoints aligned with project goals.
Selection of neuronal model and electrophysiological approach.
Stable recordings with rigorous acceptance criteria.
Functional interpretation at single-cell and network levels.