Evidence map›Paper›PMID 35354827›Full record

ArticleScientific data2022

Accumulation-depuration data collection in support of toxicokinetic modelling.

Aude Ratier, Sandrine Charles

Abstract read
In one paragraph

Article in Scientific data, 2022. 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

2 authors.

Aude RatierUniversité de Lyon, Université Lyon 1, CNRS UMR5558, Laboratoire de Biométrie et Biologie Evolutive, 69100, Villeurbanne, France.
Sandrine CharlesUniversité de Lyon, Université Lyon 1, CNRS UMR5558, Laboratoire de Biométrie et Biologie Evolutive, 69100, Villeurbanne, France. sandrine.charles@univ-lyon1.fr.ORCID 0000-0003-4604-0166

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulatory bodies require bioaccumulation evaluation of chemicals within organisms to better assess toxic risks. Toxicokinetic (TK) data are particularly useful in relating the chemical exposure to the accumulation and depuration processes happening within organisms. TK models are used to predict internal concentrations when experimental data are lacking or difficult to access, such as within target tissues. The bioaccumulative property of chemicals is quantified by metrics calculated from TK model parameters after fitting to data collected via bioaccumulation tests. In bioaccumulation tests, internal concentrations of chemicals are measured within organisms at regular time points during accumulation and depuration phases. The time course is captured by TK model parameters thus providing bioaccumulation metrics. But raw TK data remain difficult to access, most often provided within papers as plots. To increase availability of TK data, we developed an innovative database from data extracted in the scientific literature to support TK modelling. Freely available, our database can dynamically evolve thanks to any researcher interested in sharing data to be findable, accessible, interoperable and reusable.

Identifiers

PMID35354827
PMCPMC8967850

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.