Evidence map›Paper›PMID 31811386›Full record

ArticleJournal of materials science. Materials in medicine2019

Assessing two-way interactions between cells and inorganic nanoparticles.

C Cristallini, N Barbani, S Bianchi, S Maltinti, A Baldassare, R Ishak, M Onor, L Ambrosio, V Castelvetro, M G Cascone

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of materials science. Materials in medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

10 authors.

C CristalliniInstitute for Chemical and Physical Processes, IPCF ss Pisa, CNR, c/o Largo Lucio Lazzarino, 56126, Pisa, Italy. caterina.cristallini@cnr.it.
N BarbaniInstitute for Chemical and Physical Processes, IPCF ss Pisa, CNR, c/o Largo Lucio Lazzarino, 56126, Pisa, Italy.
S BianchiDepartment of Chemistry and Industrial Chemistry, DCCI, University of Pisa, via Giuseppe Moruzzi, 13, 56124, Pisa, Italy.
S MaltintiDepartment of Civil and Industrial Engineering, DICI, University of Pisa, Largo Lucio Lazzarino, Largo Lucio Lazzarino, 56126, Pisa, Italy.
A BaldassareDepartment of Civil and Industrial Engineering, DICI, University of Pisa, Largo Lucio Lazzarino, Largo Lucio Lazzarino, 56126, Pisa, Italy.
R IshakDepartment of Civil and Industrial Engineering, DICI, University of Pisa, Largo Lucio Lazzarino, Largo Lucio Lazzarino, 56126, Pisa, Italy.
M OnorInstitute of Chemistry of Organometallic Compounds, ICCOM uos Pisa, CNR, via Giuseppe Moruzzi, 1, 56124, Pisa, Italy.
L AmbrosioInstitute for Polymers, Composites and Biomaterials, IPCB, CNR, via Campi Flegrei, 34, 80078, Pozzuoli, NA, Italy.
V CastelvetroDepartment of Chemistry and Industrial Chemistry, DCCI, University of Pisa, via Giuseppe Moruzzi, 13, 56124, Pisa, Italy.
M G CasconeDepartment of Civil and Industrial Engineering, DICI, University of Pisa, Largo Lucio Lazzarino, Largo Lucio Lazzarino, 56126, Pisa, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A safe and effective use of nanoparticles in biology and medicine requires a thorough understanding, down to the molecular level, of how nanoparticles interact with cells in the physiological environment. This study evaluated the two-way interaction between inorganic nanomaterials (INMs) and cells from A549 human lung carcinoma cell line. The interaction between silica and zinc oxide INMs and cells was investigated using both standard methods and advanced characterization techniques. The effect of INMs on cell properties was evaluated in terms of cell viability, chemical modifications, and volume changes. The effect of cells and culture medium on INMs was evaluated using dynamic light scattering (DLS), scanning electron microscopy and energy-dispersive X-ray spectroscopy (SEM-EDS), high performance liquid chromatography (HPLC), gas chromatography-mass spectroscopy (GC-MS), Fourier transform infrared spectroscopy (FTIR), and thermogravimetric analysis (TGA). No cytotoxic effect was detected in the case of silicon oxide INMs, while for high doses of zinc oxide INMs a reduction of cell survival was observed. Also, increased cell volume was recorded after 24 h incubation of cells with zinc oxide INMs. A better dimensional homogeneity and colloidal stability was observed by DLS for silicon oxide INMs than for zinc oxide INMs. SEM-EDS analysis showed the effectiveness of the adopted dispersion procedure and confirmed in the case of zinc oxide INMs the presence of residual substances derived from organosilane coating. HPLC and GC-MS performed on INMs aqueous dispersions after 24 h incubation showed an additional peak related to the presence of an organic contaminant only in the case of zinc oxide INMs. FTIR Chemical Imaging carried out directly on the cells showed, in case of incubation with zinc oxide INMs, a modification of the spectra in correspondence of phospholipids, nucleic acids and proteins characteristic absorption bands when compared with untreated cells. Overall, our results confirm the importance of developing new experimental methods and techniques for improving the knowledge about the biosafety of nanomaterials.

Indexed as

A549 CellsCell SizeCell SurvivalHumansNanoparticlesSpectroscopy, Fourier Transform Infrared

Identifiers

What OpenQuestion holds

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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.