Evidence map›Paper›PMID 40993324›Full record

ArticleCommunications engineering2025

An engineered culture vessel and flow system to improve the in vitro analysis of volatile organic compounds.

Jarrett Eshima, Taylor R Pennington, Youssef Abdellatif, Angela Ponce Olea, Joel F Lusk, Benjamin D Ambrose, Ethan Marschall, Christopher Miranda, Paula Phan, Christina Aridi and 1 more

Abstract read
In one paragraph

Article in Communications engineering, 2025. 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. 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

11 authors.

Jarrett EshimaSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, 85287, USA.ORCID http://orcid.org/0000-0003-1111-9069
Taylor R PenningtonSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, 85287, USA.
Youssef AbdellatifSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, 85287, USA.
Angela Ponce OleaSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, 85287, USA.
Joel F LuskSchool for Engineering of Matter, Transport, and Energy, Arizona State University, Tempe, AZ, 85287, USA.
Benjamin D AmbroseThe College of Liberal Arts and Sciences, Arizona State University, Tempe, AZ, 85287, USA.ORCID http://orcid.org/0009-0007-8481-398X
Ethan MarschallSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, 85287, USA.ORCID http://orcid.org/0000-0002-8996-2657
Christopher MirandaSchool of Humanities and Sciences, Department of Biology, Stanford University, Stanford, CA, 94305, USA.
Paula PhanSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, 85287, USA.ORCID http://orcid.org/0009-0001-8421-2726
Christina AridiSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, 85287, USA.
Barbara S SmithSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, 85287, USA. BarbaraSmith@asu.edu.ORCID http://orcid.org/0000-0003-1758-624X

Funding

ADHS | Arizona Biomedical Research Commission (ABRC) ADHS18-198858
6 · The paper itself

Abstract

Volatile organic compounds (VOCs) are a biologically important subset of an organism's metabolome, yet in vitro techniques for the analysis of these small molecules vary substantially in practice, restricting the interpretation of study findings. Here, we present an engineered culture tool, termed the "Biodome", designed to enhance endogenous analyte recovery by integrating dynamic headspace sampling methodology for the recovery of VOCs from biological cultures. We validate the functionality of the device for in vitro volatile metabolomics utilizing computational modeling and fluorescent imaging of mammalian cell culture. Leveraging comprehensive two-dimensional gas chromatography coupled with a time-of-flight mass spectrometer and the enhanced sampling capabilities afforded by our tool, we identify 14 statistically significant VOCs not found in the media or exogenously derived from the sampling method, four of which have not been previously reported in vitro. To demonstrate applicability beyond mammalian cell culture, we assess the production of VOCs throughout the log and stationary phases of growth in ampicillin-resistant DH5α Escherichia coli. We identified 19 compounds with results supporting endogenous production, two of which had not previously associated with E. coli, 3-Octanone and 3-Tridecanone. Our findings emphasize the improved capabilities of the Biodome for in vitro volatile metabolomics.

Identifiers

PMID40993324
PMCPMC12460885

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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.