Evidence map›Paper›PMID 31562913›Full record

ArticleToxicology letters2019

Acrylonitrile butadiene styrene (ABS) and polycarbonate (PC) filaments three-dimensional (3-D) printer emissions-induced cell toxicity.

Mariana T Farcas, Aleksandr B Stefaniak, Alycia K Knepp, Lauren Bowers, William K Mandler, Michael Kashon, Stephen R Jackson, Todd A Stueckle, Jenifer D Sisler, Sherri A Friend and 6 more

Open access · greenAbstract read
In one paragraph

Article in Toxicology letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
5.6field-weighted citation impact, top 4% of its field
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

39 citing papers in PubMed, 88 citations in OpenAlex.

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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

16 authors at 3 institutions in 1 country.

Mariana T FarcasPathology and Physiology Branch, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA; Pharmaceutical and Pharmacological Sciences, School of Pharmacy, West Virginia University, Morgantown, WV, 26505, USA. Electronic address: woe7@cdc.gov.
Aleksandr B StefaniakField Studies Branch, Respiratory Health Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA. Electronic address: boq9@cdc.gov.
Alycia K KneppField Studies Branch, Respiratory Health Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA. Electronic address: ydt0@cdc.gov.
Lauren BowersField Studies Branch, Respiratory Health Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA. Electronic address: mju3@cdc.gov.
William K MandlerPathology and Physiology Branch, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA. Electronic address: oex1@cdc.gov.
Michael KashonBiostatistics and Epidemiology Branch, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA. Electronic address: mqk1@cdc.gov.
Stephen R JacksonExposure Assessment Branch, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA. Electronic address: yif8@cdc.gov.
Todd A StueckleAllergy and Clinical Immunology Branch, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA. Electronic address: jux5@cdc.gov.
Jenifer D SislerPathology and Physiology Branch, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA. Electronic address: sislerj@gmail.com.
Sherri A FriendPathology and Physiology Branch, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA. Electronic address: shf8@cdc.gov.
Chaolong QiEngineering and Physical Hazards Branch, Division of Applied Research & Technology, National Institute for Occupational Safety and Health, Cincinnati, OH, USA. Electronic address: hif1@cdc.gov.
Duane R HammondEngineering and Physical Hazards Branch, Division of Applied Research & Technology, National Institute for Occupational Safety and Health, Cincinnati, OH, USA. Electronic address: ahz0@cdc.gov.
Treye A ThomasOffice of Hazard Identification and Reduction, U.S. Consumer Product Safety Commission, Rockville, MD, USA. Electronic address: tthomas@cpsc.gov.
Joanna MathesonOffice of Hazard Identification and Reduction, U.S. Consumer Product Safety Commission, Rockville, MD, USA. Electronic address: jmatheson@cpsc.gov.
Vincent CastranovaPharmaceutical and Pharmacological Sciences, School of Pharmacy, West Virginia University, Morgantown, WV, 26505, USA. Electronic address: vcastran@hsc.wvu.edu.
Yong QianPathology and Physiology Branch, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA. Electronic address: yaq2@cdc.gov.
National Institute for Occupational Safety and Health · USUnited States Consumer Product Safety Commission · USWest Virginia University · US

Funding

West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Laura F. Gibson · 2012 to 2026
$81.0M
NIGMS NIH HHS U54 GM104942
6 · The paper itself

Abstract

During extrusion of some polymers, fused filament fabrication (FFF) 3-D printers emit billions of particles per minute and numerous organic compounds. The scope of this study was to evaluate FFF 3-D printer emission-induced toxicity in human small airway epithelial cells (SAEC). Emissions were generated from a commercially available 3-D printer inside a chamber, while operating for 1.5 h with acrylonitrile butadiene styrene (ABS) or polycarbonate (PC) filaments, and collected in cell culture medium. Characterization of the culture medium revealed that repeat print runs with an identical filament yield various amounts of particles and organic compounds. Mean particle sizes in cell culture medium were 201 ± 18 nm and 202 ± 8 nm for PC and ABS, respectively. At 24 h post-exposure, both PC and ABS emissions induced a dose dependent significant cytotoxicity, oxidative stress, apoptosis, necrosis, and production of pro-inflammatory cytokines and chemokines in SAEC. Though the emissions may not completely represent all possible exposure scenarios, this study indicate that the FFF could induce toxicological effects. Further studies are needed to quantify the detected chemicals in the emissions and their corresponding toxicological effects.

Indexed as

Printing, Three-DimensionalAcrylic ResinsApoptosisButadienesCells, CulturedCytokinesDose-Response Relationship, DrugEpithelial CellsHumansInflammation MediatorsNanoparticlesNecrosisOxidative StressParticle SizePolycarboxylate CementPolystyrenesABS resinAcrylic ResinsButadienesCytokinesInflammation MediatorspolycarbonatePolycarboxylate CementPolystyrenesEmerging technologiesInflammatory responseIn vitro toxicityPrinter emitted nanoparticles

Identifiers

PMID31562913
PMCPMC7490755
OpenAlexW2975622149

What OpenQuestion holds

Textmetadata
LicenceTDM
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.