Evidence map›Paper›PMID 33243293›Full record

ArticleParticle and fibre toxicology2020

The pulmonary toxicity of carboxylated or aminated multi-walled carbon nanotubes in mice is determined by the prior purification method.

Alexia J Taylor-Just, Mark D Ihrie, Katherine S Duke, Ho Young Lee, Dorothy J You, Salik Hussain, Vamsi K Kodali, Christina Ziemann, Otto Creutzenberg, Adriana Vulpoi and 6 more

Abstract read
In one paragraph

Article in Particle and fibre toxicology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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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.

Alexia J Taylor-JustToxicology Program, Department of Biological Sciences, North Carolina State University, 850 Main Campus Drive, Suite 1104, Toxicology Building, Raleigh, NC, 27606, USA.
Mark D IhrieToxicology Program, Department of Biological Sciences, North Carolina State University, 850 Main Campus Drive, Suite 1104, Toxicology Building, Raleigh, NC, 27606, USA.
Katherine S DukeToxicology Program, Department of Biological Sciences, North Carolina State University, 850 Main Campus Drive, Suite 1104, Toxicology Building, Raleigh, NC, 27606, USA.
Ho Young LeeToxicology Program, Department of Biological Sciences, North Carolina State University, 850 Main Campus Drive, Suite 1104, Toxicology Building, Raleigh, NC, 27606, USA.
Dorothy J YouToxicology Program, Department of Biological Sciences, North Carolina State University, 850 Main Campus Drive, Suite 1104, Toxicology Building, Raleigh, NC, 27606, USA.
Salik HussainDepartment of Physiology and Pharmacology, School of Medicine, West Virginia University, Morgantown, WV, USA.
Vamsi K KodaliDepartment of Physiology and Pharmacology, School of Medicine, West Virginia University, Morgantown, WV, USA.
Christina ZiemannFraunhofer Institute for Toxicology and Experimental Medicine ITEM, Hannover, Germany.
Otto CreutzenbergFraunhofer Institute for Toxicology and Experimental Medicine ITEM, Hannover, Germany.
Adriana VulpoiInterdisciplinary Research Institute in Bio-Nano-Sciences, Babes Bolyai University, Cluj-Napoca, Romania.
Flaviu TurcuInterdisciplinary Research Institute in Bio-Nano-Sciences, Babes Bolyai University, Cluj-Napoca, Romania.
Monica PotaraInterdisciplinary Research Institute in Bio-Nano-Sciences, Babes Bolyai University, Cluj-Napoca, Romania.
Milica TodeaInterdisciplinary Research Institute in Bio-Nano-Sciences, Babes Bolyai University, Cluj-Napoca, Romania.
Sybille van den BruleLouvain centre for Toxicology and Applied Pharmacology (LTAP), Institut de Recherche Expérimentale et Clinique (IREC), Université catholique de Louvain (UCL), Brussels, Belgium.
Dominique LisonLouvain centre for Toxicology and Applied Pharmacology (LTAP), Institut de Recherche Expérimentale et Clinique (IREC), Université catholique de Louvain (UCL), Brussels, Belgium.
James C BonnerToxicology Program, Department of Biological Sciences, North Carolina State University, 850 Main Campus Drive, Suite 1104, Toxicology Building, Raleigh, NC, 27606, USA. jcbonner@ncsu.edu.ORCID 0000-0002-4574-9782

Funding

TRAINING IN BIOCHEMICAL AND ENVIRONMENTAL TOXICOLOGYT32ES007046 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Seth William Kullman · 1985 to 2026
$5.1M
Inflammatory cross-talk between heat events and air pollutionR01ES031253 · NIEHS · WEST VIRGINIA UNIVERSITY · PI HUSSAIN, SALIK · 2020 to 2024
$3.5M
NIEHS NIH HHS R01 ES031253NIEHS NIH HHS T32 ES007046
6 · The paper itself

Abstract

backgroundInhalation of multi-walled carbon nanotubes (MWCNTs) poses a potential risk to human health. In order to safeguard workers and consumers, the toxic properties of MWCNTs need to be identified. Functionalization has been shown to either decrease or increase MWCNT-related pulmonary injury, depending on the type of modification. We, therefore, investigated both acute and chronic pulmonary toxicity of a library of MWCNTs derived from a common pristine parent compound (NC7000).

methodsMWCNTs were thermally or chemically purified and subsequently surface functionalized by carboxylation or amination. To evaluate pulmonary toxicity, male C57BL6 mice were dosed via oropharyngeal aspiration with either 1.6 or 4 mg/kg of each MWCNT type. Mitsui-7 MWCNT was used as a positive control. Necropsy was performed at days 3 and 60 post-exposure to collect bronchoalveolar lavage fluid (BALF) and lungs.

resultsAt day 3 all MWCNTs increased the number of neutrophils in BALF. Chemical purification had a greater effect on pro-inflammatory cytokines (IL-1β, IL-6, CXCL1) in BALF, while thermal purification had a greater effect on pro-fibrotic cytokines (CCL2, OPN, TGF-β1). At day 60, thermally purified, carboxylated MWCNTs had the strongest effect on lymphocyte numbers in BALF. Thermally purified MWCNTs caused the greatest increase in LDH and total protein in BALF. Furthermore, the thermally purified and carboxyl- or amine-functionalized MWCNTs caused the greatest number of granulomatous lesions in the lungs. The physicochemical characteristics mainly associated with increased toxicity of the thermally purified derivatives were decreased surface defects and decreased amorphous content as indicated by Raman spectroscopy.

conclusionsThese data demonstrate that the purification method is an important determinant of lung toxicity induced by carboxyl- and amine-functionalized MWCNTs.

Indexed as

Administration, InhalationAir PollutantsAnimalsBronchoalveolar Lavage FluidCytokinesInhalation ExposureLungLung InjuryMiceMice, Inbred C57BLNanotubes, CarbonTransforming Growth Factor beta1Air PollutantsCytokinesNanotubes, CarbonTransforming Growth Factor beta1Carbon nanotubesFibrosisFunctionalizationLung injuryPurification

Identifiers

PMID33243293
PMCPMC7690083

What OpenQuestion holds

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LicenceCC BY
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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.