Evidence map›Paper›PMID 41635987›Full record

ArticleInhalation toxicology2026

Application of a human bronchoepithelial-air-liquid interface model to assess respiratory hazard of VOCs using a benchmark concentration modeling approach.

Olivia C G Lampe, Eva C M Vitucci, Carolyn L Cannon, Weihsueh A Chiu, Natalie M Johnson

Abstract read
In one paragraph

Article in Inhalation toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Olivia C G LampeDepartment of Environmental and Occupational Health, Texas A&M University, College Station, TX, USA.
Eva C M VitucciDepartment of Environmental and Occupational Health, Texas A&M University, College Station, TX, USA.
Carolyn L CannonDepartment of Microbial Pathogenesis and Immunology, Texas A&M University, Bryan, TX, USA.
Weihsueh A ChiuInterdisciplinary Program in Toxicology, Texas A&M University, College Station, TX, USA.
Natalie M JohnsonDepartment of Environmental and Occupational Health, Texas A&M University, College Station, TX, USA.

Funding

Single cell, multi-parametric high throughput platform to classify endocrine disruptor potential of mixturesP42ES027704 · NIEHS · TEXAS A&M UNIVERSITY · PI Efstratios Pistikopoulos · 2017 to 2026
$21.2M
Texas A&M Center for Environmental Health Research (TiCER)P30ES029067 · NIEHS · TEXAS A&M UNIVERSITY · PI Sakhila Banu · 2019 to 2026
$13.0M
Regulatory Science in Environmental Health and ToxicologyT32ES026568 · NIEHS · TEXAS A&M UNIVERSITY · PI Weihsueh A Chiu, Natalie M Johnson · 2016 to 2026
$3.8M
NIEHS NIH HHS P30 ES029067NIEHS NIH HHS P42 ES027704NIEHS NIH HHS T32 ES026568
6 · The paper itself

Abstract

objectiveVolatile organic compounds (VOCs) are prevalent in both indoor and outdoor environments and have been linked to health effects. This study aimed to assess VOC-induced effects on the respiratory epithelium using an

methodsA human bronchial epithelial cell line, 16HBE, was cultured at ALI and exposed to relevant concentrations of two representative VOCs, acrolein or formic acid, and matched filtered air (control) in a CelTox exposure system for two hours to replicate an acute inhalation exposure. Cells were allowed to recover for 24 h before cell lysate and culture media were collected for analysis.

resultsCytotoxicity, based on LDH activity, significantly increased at the highest doses tested for both VOCs. A dose-dependent increase in barrier permeability was observed for confluent cells exposed to acrolein and formic acid. Acrolein and formic acid exposure induced

conclusionCollectively, these findings demonstrate that this model is a plausible

Indexed as

AcroleinBronchiEpithelial CellsFormatesModels, BiologicalRespiratory MucosaVolatile Organic CompoundsCell LineCell SurvivalDose-Response Relationship, DrugHeme Oxygenase-1HumansInterleukin-8Tumor Necrosis Factor-alphaAcroleinFormatesformic acidHeme Oxygenase-1HMOX1 protein, humanInterleukin-8Tumor Necrosis Factor-alphaVolatile Organic CompoundsAcroleinbarrier functionbenchmark dose modelingformic acidvolatile organic compounds (VOCs)

Identifiers

PMID41635987
PMCPMC12989087

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LicenceCC BY-NC-ND
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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.