Devices

128-channel, eight-shank NET modules assembled into distributed rodent cortical arrays. The 2022 paper shows 1,024- and 1,280-channel placements, thousands of sorted units and module follow-up to 290 days.

Device — Intracortical

Modular NET high-density arrays

NET · ultraflexible · modular · Rice · UCSF · high density · cortex · rodent · academic · preclinical

Modular NET high-density arrays

A larger modular recording platform built from ultraflexible nanoelectronic threads. Zhao and colleagues’ paper was published online on 3 October 2022 in Nature Biomedical Engineering. The listed affiliations include Rice University’s electrical and computer engineering, bioengineering and NeuroEngineering Initiative, and UCSF neuroscience and neurological surgery.

This is a hardware development beyond the 2017 NET-50 and NET-10 probes, not a claim that the original four- or eight-contact threads had thousands of channels.

Module and recording system

Figure 1 shows 128-channel modules, each with eight shanks carrying 16 intracortical recording sites. The study used three NET array designs. Modules were assembled for sequential implantation, one module at a time, using stereotaxic micromanipulators.

The article’s Extended Data Figure 3 shows a NET module linked through a flexible printed circuit to a stackable 128-channel headstage. Eight modules form the pictured 1,024-channel recording system. A freely moving rat carries those headstages in a 3D-printed case. The system is not a fully implanted wireless human BCI.

Keep channels and units separate

ExampleWhat the paper reports
Figure 1, ratEight 128-channel modules, 1,024 channels total
Figure 1, mouse visual cortex8 x 8 x 16 layout, 1,024 channels; targeted module spacing 150 µm
Figure 3, mouse visual cortex80 shanks, 1,280 channels; 1,355 recorded units
Figure 6, distributed mouse recording144 shanks; representative raster of 2,548 units across visual, sensory and motor cortex

A recording site can contribute to more than one sorted unit. Unit count is not electrode count, and a targeted placement or reconstructed location is not a measured fabrication mask. The abstract reports several thousand neurons at densities around 1,000 units per cubic millimetre across the demonstrated rodent recordings.

Duration and tissue evidence

Figure 7 follows 21 modules: 16 for 145 days and five for 290 days. Module-averaged impedance, spike amplitude, signal-to-noise ratio and single- and multi-unit yield remained stable over the reported durations after initial changes within 60 days. These are module-averaged results, not proof that every channel or every neuron stayed unchanged.

Extended Data Figure 1 describes one mouse implanted with ten type-I modules at 150 µm inter-shank and 250 µm inter-module spacing. The authors report no observable scarring and no significant difference in the sampled local neuron densities. That tissue analysis uses a different placement from Figure 1’s targeted 150 µm module spacing; the numbers are not merged into one universal spacing.

Applications and limits

The experiments include visual decoding, behavioural-state prediction and optogenetic stimulation alongside recording. The paper uses electrical correlations and timing to infer neural coupling and directional information flow. It does not directly prove anatomical connections between every correlated pair.

The source describes head-fixed mice and freely moving rats. No human implant, clinical outcome or assistive-device control is established here. Longitudinal unit yield and network stability are different from tracking the same single neurons for every recording day.

No model is added from figure photographs alone. Exact full shank outlines, electrode coordinates and trace routing for the three designs are not reconstructed in this entry.

Sources

This entry uses the accessible primary abstract, figure captions and extended-data captions. It does not claim to reproduce every fabrication method from the full article.