Evidence map›Paper›PMID 32384606›Full record

ArticleNanomaterials (Basel, Switzerland)2020

Determination of Total Silicon and SiO

Federica Aureli, Maria Ciprotti, Marilena D'Amato, Emanueli do Nascimento da Silva, Stefano Nisi, Daniele Passeri, Angela Sorbo, Andrea Raggi, Marco Rossi, Francesco Cubadda

Open access · goldAbstract read
In one paragraph

Article in Nanomaterials (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 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

10 authors at 4 institutions in 2 countries.

Federica AureliIstituto Superiore di Sanità-National Institute of Health, 00161 Rome, Italy.
Maria CiprottiIstituto Superiore di Sanità-National Institute of Health, 00161 Rome, Italy.
Marilena D'AmatoIstituto Superiore di Sanità-National Institute of Health, 00161 Rome, Italy.
Emanueli do Nascimento da SilvaDepartment of Chemistry, Institute of Exact and Biological Sciences, Federal University of Ouro Preto, Ouro Preto 35400000, MG, Brazil.ORCID 0000-0002-7053-7132
Stefano NisiGran Sasso National Laboratory, National Institute of Nuclear Physics (LNGS-INFN), 67100 Assergi (AQ), Italy.
Daniele PasseriDepartment of Basic and Applied Sciences for Engineering, University of Rome Sapienza, 00161 Rome, Italy.ORCID 0000-0001-8189-1359
Angela SorboIstituto Superiore di Sanità-National Institute of Health, 00161 Rome, Italy.
Andrea RaggiIstituto Superiore di Sanità-National Institute of Health, 00161 Rome, Italy.
Marco RossiDepartment of Basic and Applied Sciences for Engineering, University of Rome Sapienza, 00161 Rome, Italy.ORCID 0000-0001-7603-1805
Francesco CubaddaIstituto Superiore di Sanità-National Institute of Health, 00161 Rome, Italy.ORCID 0000-0003-3454-7947
Istituto Superiore di Sanità · ITSapienza University of Rome · ITIstituto Nazionale di Fisica Nucleare, Laboratori Nazionali del Gran Sasso · ITUniversidade Federal de Ouro Preto · BR

Funding

Executive Agency for Health and Consumers 2009 21 01
6 · The paper itself

Abstract

Synthetic amorphous silica (SAS), manufactured in pyrogenic or precipitated form, is a nanomaterial with a widespread use as food additive (E 551). Oral exposure to SAS results from its use in food and dietary supplements, pharmaceuticals and toothpaste. Recent evidence suggests that oral exposure to SAS may pose health risks and highlights the need to address the toxic potential of SAS as affected by the physicochemical characteristics of the different forms of SAS. For this aim, investigating SAS toxicokinetics is of crucial importance and an analytical strategy for such an undertaking is presented. The minimization of silicon background in tissues, control of contamination (including silicon release from equipment), high-throughput sample treatment, elimination of spectral interferences affecting inductively coupled plasma mass spectrometry (ICP-MS) silicon detection, and development of analytical quality control tools are the cornerstones of this strategy. A validated method combining sample digestion with silicon determination by reaction cell ICP-MS is presented. Silica particles are converted to soluble silicon by microwave dissolution with mixtures of HNO

Indexed as

ADMEanalytical quality controlinductively coupled plasma mass spectrometrymicrowave digestionpolyatomic interferencessilicon determinationsingle particle ICP-MSsynthetic amorphous silicatissue levels

Identifiers

PMID32384606
PMCPMC7279390
OpenAlexW3021186168

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.