Silicon Nanowire Mats Enable Advanced Bioelectrical Recordings in Primary DRG Cell Cultures

Primary dorsal root ganglion (DRG) cell cultures provide a valuable model for studying in vitro sensory transduction, neuropathies, and chronic pain, as they replicate the in vivo heterogeneity of DRG neurons and non-neuronal cells. However, traditional patch-clamp techniques are invasive and cannot capture the collective cell dynamics. While planar multielectrode arrays (MEAs) offer a non-invasive alternative, they suffer from poor cell-electrode coupling and limited resolution for identifying specific DRG neuronal types like C-fiber nociceptors, key targets in chronic pain research. This work demonstrates that silicon nanowire (SiNW) mat-based MEAs, while maintaining their reduced invasiveness, enable continuous intracellular recordings from neurons in primary rat DRG cell cultures. Supported by a cortical astrocyte feeder layer, SiNW mats promote DRG neuron and glial cell growth preserving cells' in vivo morphological and functional characteristics. Integrated into a compartmentalized MEA, they enable reliable recordings of drug-modulated neuronal activity alongside a baseline related to the astrocyte layer. The recorded signals exhibit characteristics of intracellular action potentials, suggesting spontaneous intracellular access by SiNWs. Distinct electrophysiological signatures allow identifying C-fiber nociceptors, as confirmed by patch-clamp measurements. This platform represents a powerful tool for investigating in vitro pain mechanisms, with potential applications in preclinical pain research and pharmacological translational studies.