Evidence map›Paper›PMID 35644618›Full record

ArticleParticle and fibre toxicology2022

Impact of in vitro digested zinc oxide nanoparticles on intestinal model systems.

Anna Mittag, Alina Singer, Christian Hoera, Martin Westermann, Alexander Kämpfe, Michael Glei

Open access · goldAbstract read
In one paragraph

Article in Particle and fibre toxicology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 19 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

6 authors at 2 institutions in 1 country.

Anna MittagDepartment of Applied Nutritional Toxicology, Institute of Nutritional Sciences, Friedrich Schiller University, Jena, Germany. anna.mittag@uni-jena.de.ORCID 0000-0001-5517-5113
Alina SingerDepartment of Applied Nutritional Toxicology, Institute of Nutritional Sciences, Friedrich Schiller University, Jena, Germany.
Christian HoeraSwimming and Bathing Pool Water, Chemical Analytics, German Environment Agency, Bad Elster, Germany.
Martin WestermannElectron Microscopy Center, University Hospital, Friedrich Schiller University, Jena, Germany.
Alexander KämpfeSwimming and Bathing Pool Water, Chemical Analytics, German Environment Agency, Bad Elster, Germany.
Michael GleiDepartment of Applied Nutritional Toxicology, Institute of Nutritional Sciences, Friedrich Schiller University, Jena, Germany.ORCID 0000-0003-4740-112X
Friedrich Schiller University Jena · DEGerman Environment Agency · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundZinc oxide nanoparticles (ZnO NP) offer beneficial properties for many applications, especially in the food sector. Consequently, as part of the human food chain, they are taken up orally. The toxicological evaluation of orally ingested ZnO NP is still controversial. In addition, their physicochemical properties can change during digestion, which leads to an altered biological behaviour. Therefore, the aim of our study was to investigate the fate of two different sized ZnO NP (< 50 nm and < 100 nm) during in vitro digestion and their effects on model systems of the intestinal barrier. Differentiated Caco-2 cells were used in mono- and coculture with mucus-producing HT29-MTX cells. The cellular uptake, the impact on the monolayer barrier integrity and cytotoxic effects were investigated after 24 h exposure to 123-614 µM ZnO NP.

resultsIn vitro digested ZnO NP went through a morphological and chemical transformation with about 70% free zinc ions after the intestinal phase. The cellular zinc content increased dose-dependently up to threefold in the monoculture and fourfold in the coculture after treatment with digested ZnO NP. This led to reactive oxygen species but showed no impact on cellular organelles, the metabolic activity, and the mitochondrial membrane potential. Only very small amounts of zinc (< 0.7%) reached the basolateral area, which is due to the unmodified transepithelial electrical resistance, permeability, and cytoskeletal morphology.

conclusionsOur results reveal that digested and, therefore, modified ZnO NP interact with cells of an intact intestinal barrier. But this is not associated with serious cell damage.

Indexed as

NanoparticlesZinc OxideCaco-2 CellsHumansIntestinesZincZincZinc OxideCaco-2CocultureHT29-MTXIn vitro digestionNanoparticlesToxicityTranswellZinc oxide

Identifiers

PMID35644618
PMCPMC9150335
OpenAlexW4281606563

What OpenQuestion holds

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LicenceCC BY
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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.