ArticleACS sensors2025
Inkjet-Printed 3D Sensor Arrays with FIB-Induced Electrode Refinement for Low-Noise Amperometric Recordings in hiPSC-Derived Brain Organoids.
Article in ACS sensors, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Flexible Multimodal Neural Probe with Integrated Three-Electrode Aptameric Sensing for In Vivo Monitoring of Dopamine Dynamics and Neural Activity.ACS chemical neuroscience · 2026Article
- Inkjet-Printed Rough Gold Microelectrode Arrays on Flexible Substrates for Neural Recording and Electrical Stimulation.ACS applied materials & interfaces · 2026Article
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Authors and funding
7 authors.
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Abstract
Understanding the functional connectivity and behavior of 3D cell cultures and organoids requires monitoring electrical activity across multiple planes. However, traditional planar microelectrode arrays (MEAs) are limited to surface recordings and struggle to capture signals from deeper layers. Additionally, current fabrication methods face challenges such as prolonged production times and limited design flexibility, which hinder the development of high-precision 3D electrode arrays and affect the quality of cell-electrode coupling. To overcome these obstacles, we introduce a new approach that integrates inkjet printing with focused ion beam (FIB) milling and electrodeposition, resulting in highly customizable 3D MEAs. The FIB milling enables the creation of precise electrode openings at predetermined locations, which is essential for selective recordings within the tissue. The MEAs, fabricated on glass substrates, incorporate high-aspect-ratio (up to 44:1) electrode structures with heights up to 1 mm, a pitch of 500 μm, and electrode openings of 3 and 6 μm, providing the necessary resolution for targeted measurements. Impedance and noise characteristics (down to a root-mean-square of (RMS) noise of 0.2 pA) for amperometric measurements were assessed in dependence on the electrode size. We demonstrate the effectiveness of these 3D MEAs by recording electrophysiological activity from hiPSC-derived cortical organoids (age: 24 month) both in situ and after 10 days of cultivation of the organoid directly on the MEA. This approach facilitates in vitro studies of neural activity in organoids and holds promise for high-throughput, selective amperometric analyses in normal and pathologically altered conditions.
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