Evidence map›Paper›PMID 26113973›Full record

ArticleMedical gas research2015

Pharmacokinetic analysis of the chronic administration of the inert gases Xe and Ar using a physiological based model.

Ira Katz, Jacqueline Murdock, Marc Palgen, Jan Pype, Georges Caillibotte

Open access · hybridAbstract read
In one paragraph

Article in Medical gas research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Xenon Antiaggregant Effects.Bulletin of experimental biology and medicine · 2024
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Inhaling xenon ameliorates l-dopa-induced dyskinesia in experimental parkinsonism.Movement disorders : official journal of the Movement Disorder Society · 2018
    Article
  9. New Beginnings forMedical gas research · 2016
    Article
  10. Review
  11. Gas transport duringMedical gas research · 2016
    Article
  12. What's new inMedical gas research
    Article
  13. Article
  14. Article
  15. 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

5 authors at 2 institutions in 2 countries.

Ira KatzMedical R&D, Air Liquide Santé International, Centre de Recherche Paris-Saclay, 1, chemin de la Porte des Loges, BP126 - 78354 Jouy en Josas, France ; Department of Mechanical Engineering, Lafayette College, Easton, PA 18042 USA.
Jacqueline MurdockMedical R&D, Air Liquide Santé International, Centre de Recherche Paris-Saclay, 1, chemin de la Porte des Loges, BP126 - 78354 Jouy en Josas, France.
Marc PalgenMedical R&D, Air Liquide Santé International, Centre de Recherche Paris-Saclay, 1, chemin de la Porte des Loges, BP126 - 78354 Jouy en Josas, France.
Jan PypeMedical R&D, Air Liquide Santé International, Centre de Recherche Paris-Saclay, 1, chemin de la Porte des Loges, BP126 - 78354 Jouy en Josas, France.
Georges CaillibotteMedical R&D, Air Liquide Santé International, Centre de Recherche Paris-Saclay, 1, chemin de la Porte des Loges, BP126 - 78354 Jouy en Josas, France.
Air Liquide (United Kingdom) · GBLafayette College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNew gas therapies using inert gases such as xenon and argon are being studied, which would require chronically administered repeating doses. The pharmacokinetics of this type of administration has not been addressed in the literature.

methodsA physiologically based pharmacokinetics (PBPK) model for humans, pigs, mice, and rats has been developed to investigate the unique aspects of the chronic administration of inert gas therapies. The absorption, distribution, metabolism and excretion (ADME) models are as follows: absorption in all compartments is assumed to be perfusion limited, no metabolism of the gases occurs, and excretion is only the reverse process of absorption through the lungs and exhaled.

resultsThe model has shown that there can be a residual dose, equivalent to constant administration, for chronic repeated dosing of xenon in humans. However, this is not necessarily the case for small animals used in pre-clinical studies.

conclusionsThe use of standard pharmacokinetics parameters such as area under the curve would be more appropriate to assess the delivered dose of chronic gas administration than the gas concentration in the delivery system that is typically reported in the scientific literature because species and gas differences can result in very different delivered doses.

Indexed as

ArgonHumanPharmacokineticsPigRatXenon

Identifiers

PMID26113973
PMCPMC4480577
OpenAlexW1527158506

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.