Evidence map›Paper›PMID 36296045›Full record

ArticleMicromachines2022

A Novel 3D Helical Microelectrode Array for In Vitro Extracellular Action Potential Recording.

Negar Geramifard, Jennifer Lawson, Stuart F Cogan, Bryan James Black

Abstract read
In one paragraph

Article in Micromachines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Three-dimensional microelectrode arrays forBiomedical engineering letters · 2026
    Review
  2. Decoding Pain: Next-Generation In Vitro Systems for Mechanistic Insights and Drug Discovery.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Review
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Negar GeramifardDepartment of Bioengineering, Erik Jonsson School of Engineering and Computer Science, University of Texas at Dallas, Richardson, TX 75080, USA.ORCID 0000-0002-5717-5376
Jennifer LawsonBiomedical Engineering Department, Francis College of Engineering, University of Massachusetts Lowell, Lowell, MA 01854, USA.ORCID 0000-0001-9494-6232
Stuart F CoganDepartment of Bioengineering, Erik Jonsson School of Engineering and Computer Science, University of Texas at Dallas, Richardson, TX 75080, USA.
Bryan James BlackBiomedical Engineering Department, Francis College of Engineering, University of Massachusetts Lowell, Lowell, MA 01854, USA.

Funding

Scalable Electrode Technology for High Resolution Chronic Recording of BrainR01NS104344 · NINDS · UNIVERSITY OF TEXAS DALLAS · PI COGAN, STUART F, MILLER, LEE · 2018 to 2022
$3.1M
hiPSC-based DRG Tissue Mimics on Multi-well Microelectrode Arrays as a Tissue Chip Model of Acute and Chronic NociceptionUH3TR003149 · NCATS · UNIVERSITY OF MASSACHUSETTS LOWELL · PI BLACK, BRYAN JAMES · 2021 to 2021
$845k
NIH HHS R01NS104344NIH HHS UH3TR003149
6 · The paper itself

Abstract

Recent advances in cell and tissue engineering have enabled long-term three-dimensional (3D) in vitro cultures of human-derived neuronal tissues. Analogous two-dimensional (2D) tissue cultures have been used for decades in combination with substrate integrated microelectrode arrays (MEA) for pharmacological and toxicological assessments. While the phenotypic and cytoarchitectural arguments for 3D culture are clear, 3D MEA technologies are presently inadequate. This is mostly due to the technical challenge of creating vertical electrical conduction paths (or 'traces') using standardized biocompatible materials and fabrication techniques. Here, we have circumvented that challenge by designing and fabricating a novel helical 3D MEA comprised of polyimide, amorphous silicon carbide (a-SiC), gold/titanium, and sputtered iridium oxide films (SIROF). Electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) testing confirmed fully-fabricated MEAs should be capable of recording extracellular action potentials (EAPs) with high signal-to-noise ratios (SNR). We then seeded induced pluripotent stems cell (iPSC) sensory neurons (SNs) in a 3D collagen-based hydrogel integrated with the helical MEAs and recorded EAPs for up to 28 days in vitro from across the MEA volume. Importantly, this highly adaptable design does not intrinsically limit cell/tissue type, channel count, height, or total volume.

Indexed as

3D cell culture3D microelectrodeiPSC sensory neuronsmicroelectrode arrays

Identifiers

PMID36296045
PMCPMC9611359

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.