Evidence map›Paper›PMID 26125028›Full record

ArticleBioMed research international2015

Quantification of Internalized Silica Nanoparticles via STED Microscopy.

Henrike Peuschel, Thomas Ruckelshausen, Christian Cavelius, Annette Kraegeloh

Abstract read
In one paragraph

Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 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

4 authors.

Henrike PeuschelLeibniz-Institute for New Materials (INM), Campus D2 2, 66123 Saarbruecken, Germany.
Thomas RuckelshausenLeibniz-Institute for New Materials (INM), Campus D2 2, 66123 Saarbruecken, Germany.
Christian CaveliusLeibniz-Institute for New Materials (INM), Campus D2 2, 66123 Saarbruecken, Germany.
Annette KraegelohLeibniz-Institute for New Materials (INM), Campus D2 2, 66123 Saarbruecken, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of safe engineered nanoparticles (NPs) requires a detailed understanding of their interaction mechanisms on a cellular level. Therefore, quantification of NP internalization is crucial to predict the potential impact of intracellular NP doses, providing essential information for risk assessment as well as for drug delivery applications. In this study, the internalization of 25 nm and 85 nm silica nanoparticles (SNPs) in alveolar type II cells (A549) was quantified by application of super-resolution STED (stimulated emission depletion) microscopy. Cells were exposed to equal particle number concentrations (9.2 × 10(10) particles mL(-1)) of each particle size and the sedimentation of particles during exposure was taken into account. Microscopy images revealed that particles of both sizes entered the cells after 5 h incubation in serum supplemented and serum-free medium. According to the in vitro sedimentation, diffusion, and dosimetry (ISDD) model 20-27% of the particles sedimented. In comparison, 10(2)-10(3) NPs per cell were detected intracellularly serum-containing medium. Furthermore, in the presence of serum, no cytotoxicity was induced by the SNPs. In serum-free medium, large agglomerates of both particle sizes covered the cells whereas only high concentrations (≥ 3.8 × 10(12) particles mL(-1)) of the smaller particles induced cytotoxicity.

Indexed as

Cell LineDose-Response Relationship, DrugHumansMicroscopyNanoparticlesParticle SizePulmonary AlveoliSilicon DioxideSilicon Dioxide

Identifiers

PMID26125028
PMCPMC4466362

What OpenQuestion holds

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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.