Evidence map›Paper›PMID 35854319›Full record

ArticleParticle and fibre toxicology2022

Changes of physico-chemical properties of nano-biomaterials by digestion fluids affect the physiological properties of epithelial intestinal cells and barrier models.

Giulia Antonello, Arianna Marucco, Elena Gazzano, Panagiotis Kainourgios, Costanza Ravagli, Ana Gonzalez-Paredes, Simone Sprio, Esperanza Padín-González, Mahmoud G Soliman, David Beal and 9 more

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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 28 citations in OpenAlex.

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  14. Photoresponsive Inorganic Nanomaterials in Oncology.Technology in cancer research & treatment
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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

19 authors at 8 institutions in 4 countries.

Giulia AntonelloDepartment of Chemistry, University of Turin, Via Pietro Giuria 7, 10125, Turin, Italy.
Arianna MaruccoDepartment of Life Sciences and Systems Biology, University of Turin, Via Accademia Albertina 13, 10123, Turin, Italy.
Elena GazzanoDepartment of Life Sciences and Systems Biology, University of Turin, Via Accademia Albertina 13, 10123, Turin, Italy.
Panagiotis KainourgiosResearch Unit of Advanced, Composite, Nano-Materials and Nanotechnology, School of Chemical Engineering, National Technical University of Athens, 9 Heroon Polytechniou St., 15780, Zographos, Athens, Greece.
Costanza RavagliColorobbia Consulting Srl, Headwork, Via Pietramarina, 53, 50059, Sovigliana, Vinci, FI, Italy.
Ana Gonzalez-ParedesNanovector Srl, Headwork, Via Livorno 60, 10144, Turin, Italy.
Simone SprioNational Research Council, Institute of Science and Technology for Ceramics ISTEC-CNR, Via Granarolo 64, 48018, Faenza, RA, Italy.
Esperanza Padín-GonzálezDepartment of Chemistry, Royal College of Surgeons in Ireland (RCSI), 123 St Stephen Green, Dublin 2, Ireland.
Mahmoud G SolimanDepartment of Chemistry, Royal College of Surgeons in Ireland (RCSI), 123 St Stephen Green, Dublin 2, Ireland.
David BealCEA, CNRS, IRIG, SyMMES-CIBEST, Université Grenoble Alpes, 38000, Grenoble, France.
Francesco BarberoDepartment of Chemistry, University of Turin, Via Pietro Giuria 7, 10125, Turin, Italy.
Paolo GascoNanovector Srl, Headwork, Via Livorno 60, 10144, Turin, Italy.
Giovanni BaldiColorobbia Consulting Srl, Headwork, Via Pietramarina, 53, 50059, Sovigliana, Vinci, FI, Italy.
Marie CarriereCEA, CNRS, IRIG, SyMMES-CIBEST, Université Grenoble Alpes, 38000, Grenoble, France.
Marco P MonopoliDepartment of Chemistry, Royal College of Surgeons in Ireland (RCSI), 123 St Stephen Green, Dublin 2, Ireland.
Costas A CharitidisResearch Unit of Advanced, Composite, Nano-Materials and Nanotechnology, School of Chemical Engineering, National Technical University of Athens, 9 Heroon Polytechniou St., 15780, Zographos, Athens, Greece.
Enrico BergamaschiDepartment of Public Health and Pediatrics, University of Turin, Piazza Polonia, 94, 10126, Turin, Italy.
Ivana Fenoglio *Department of Chemistry, University of Turin, Via Pietro Giuria 7, 10125, Turin, Italy. ivana.fenoglio@unito.it.
Chiara Riganti *Department of Oncology, University of Turin, Via Santena 5 bis, 10126, Turin, Italy. chiara.riganti@unito.it.
University of Turin · ITRoyal College of Surgeons in Ireland · IEColorobbia (Italy) · ITNational Technical University of Athens · GRAccademia Albertina delle Belle Arti · ITCEA Grenoble · FRInstitute of Science and Technology for Ceramics · ITUniversité Grenoble Alpes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe widespread use of nano-biomaterials (NBMs) has increased the chance of human exposure. Although ingestion is one of the major routes of exposure to NBMs, it is not thoroughly studied to date. NBMs are expected to be dramatically modified following the transit into the oral-gastric-intestinal (OGI) tract. How these transformations affect their interaction with intestinal cells is still poorly understood. NBMs of different chemical nature-lipid-surfactant nanoparticles (LSNPs), carbon nanoparticles (CNPs), surface modified Fe

resultsThe application of the in vitro SDHS modified the biocompatibility of NBMs on gastrointestinal cells. The differences between SHDS-treated and untreated NBMs could be attributed to the irreversible modification of the NBMs in the SHDS. Aggregation was detected for all NBMs regardless of their chemical nature, while pH- or enzyme-mediated partial degradation was detected for hydroxyapatite or polymer-coated iron oxide nanoparticles and lipid nanoparticles, respectively. The formation of a bio-corona, which contains proteases, was also demonstrated on all the analysed NBMs. In viability assays, undifferentiated primary cells were more sensitive than immortalised cells to digested NBMs, but neither pristine nor treated NBMs affected the intestinal barrier viability and permeability. SHDS-treated NBMs up-regulated the tight junction genes (claudin 3 and 5, occludin, zonula occludens 1) in intestinal barrier, with different patterns between each NBM, and increase the expression of both pro- and anti-inflammatory cytokines (IL-1β, TNF-α, IL-22, IL-10). Notably, none of these NBMs showed any significant genotoxic effect.

conclusionsOverall, the results add a piece of evidence on the importance of applying validated in vitro SHDS models for the assessment of NBM intestinal toxicity/biocompatibility. We propose the association of chemical and microscopic characterization, SHDS and in vitro tests on both immortalised and primary cells as a robust screening pipeline useful to monitor the changes in the physico-chemical properties of ingested NBMs and their effects on intestinal cells.

Indexed as

Biocompatible MaterialsIntestinal MucosaCaco-2 CellsDigestionHumansHydroxyapatitesLiposomesNanoparticlesPermeabilityTight JunctionsBiocompatible MaterialsHydroxyapatitesLipid NanoparticlesLiposomesBiotransformationCaco-2Gastro-intestinal barrierHCoEpiCHCT116InflammationIn vitro simulated digestionNano-biomaterialsPermeabilityToxicity

Identifiers

PMID35854319
PMCPMC9297619
OpenAlexW4285797735

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.