Evidence map›Paper›PMID 42209464›Full record

ArticleMicrosystems & nanoengineering2026

Detection of mitochondrial bioenergetics using a novel bimodal 3D microelectrode array (MEA)-based biosensor.

Randall K James, Tatiana C Hostios, Ji Chang, Aakash Patel, Faisal Bin Kashem, Isaac Johnson, Jorge Manrique Castro, James Hickman, Swaminathan Rajaraman

Abstract read
In one paragraph

Article in Microsystems & nanoengineering, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

9 authors.

Randall K James *NanoScience Technology Center, University of Central Florida, Orlando, FL, USA.ORCID http://orcid.org/0009-0000-7726-9436
Tatiana C Hostios *Burnett School of Biomedical Sciences, University of Central Florida, Orlando, FL, USA.
Ji ChangNanoScience Technology Center, University of Central Florida, Orlando, FL, USA.ORCID http://orcid.org/0009-0009-4355-2693
Aakash PatelNanoScience Technology Center, University of Central Florida, Orlando, FL, USA.
Faisal Bin KashemNanoScience Technology Center, University of Central Florida, Orlando, FL, USA.
Isaac JohnsonNanoScience Technology Center, University of Central Florida, Orlando, FL, USA.
Jorge Manrique CastroElectrical and Computer Engineering Department, The University of Texas at El Paso, El Paso, TX, USA.ORCID http://orcid.org/0000-0002-9248-3120
James HickmanNanoScience Technology Center, University of Central Florida, Orlando, FL, USA.ORCID http://orcid.org/0000-0002-1621-3006
Swaminathan RajaramanNanoScience Technology Center, University of Central Florida, Orlando, FL, USA. Swaminathan.Rajaraman@ucf.edu.

Funding

Microphysiological Model of Human Cardiac Sympathetic InnervationR01HL164936 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI KIM, DEOK-HO, KWON, CHULAN · 2022 to 2025
$3.2M
U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL164936
6 · The paper itself

Abstract

Developing new label-free paradigms for functional assays in biomedical research has the potential to catalyze efforts in drug discovery and improve the understanding of complex disorders. Mitochondria are an essential organelle in nearly every eukaryotic organism that perform vital functions such as adenosine triphosphate (ATP) production, redox signaling, reactive oxygen species (ROS) homeostasis and regulation of programmed cell death. These activities are regulated by electrophysiological processes that occur in the inner mitochondrial membrane (IMM) and outer mitochondrial membrane (OMM) in response to metabolic demands, making them an important physiological marker for bioenergetic studies. Mitochondria dysfunction is an early pathological biomarker of complex diseases, such as diabetes, neurodegeneration, myopathy, cancer, and cardiovascular disease. Built atop a novel microfabrication strategy for 3D Microelectrode Arrays (MEAs), we demonstrate a 3D mitochondria biosensor capable of bimodal sensing of mitochondrial electrophysiology from the OMM and IMM using electrochemical impedance spectroscopy (EIS) and electrophysiology recordings. Data obtained using EIS displays impedance magnitude and phase characterization of mitochondria isolated from NIH3T3 and induced pluripotent stem cells (iPSC) models, these measurements represent the major functional outputs of cellular respiration and electron transport chain (ETC) activity through the detection of conductive and capacitive properties of the IMM. Additionally, time-resolved electrophysiological recordings from an NIH3T3 derived mitochondrial pellet captured sub-millisecond voltage transients, establishing a complementary real-time electrophysiological profile of mitochondrial membrane activity that can be attributed voltage dependent anion channel (VDAC) gating or IMM potential dynamics.

Identifiers

PMID42209464
PMCPMC13219634

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.