Evidence map›Paper›PMID 35092809›Full record

ArticleToxicology letters2022

Toxicity of high-molecular-weight polyethylene glycols in Sprague Dawley rats.

Jia-Long Fang, Michelle M Vanlandingham, Frederick A Beland, Robert P Felton, Mackean P Maisha, Greg R Olson, Ralph E Patton, Amy S Rosenberg, Gonçalo Gamboa da Costa

Open access · greenAbstract read
In one paragraph

Article in Toxicology letters, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

8 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Polyethylene Glycols Stimulate CaInternational journal of nanomedicine · 2024
    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

9 authors at 2 institutions in 1 country.

Jia-Long FangDivision of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, AR 72079, USA. Electronic address: jia-long.fang@fda.hhs.gov.
Michelle M VanlandinghamDivision of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, AR 72079, USA.
Frederick A BelandDivision of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, AR 72079, USA.
Robert P FeltonDivision of Bioinformatics and Biostatistics, National Center for Toxicological Research, Jefferson, AR 72079, USA.
Mackean P MaishaDivision of Bioinformatics and Biostatistics, National Center for Toxicological Research, Jefferson, AR 72079, USA.
Greg R OlsonToxicologic Pathology Associates, Inc., National Center for Toxicological Research, Jefferson, AR 72079, USA.
Ralph E PattonToxicologic Pathology Associates, Inc., National Center for Toxicological Research, Jefferson, AR 72079, USA.
Amy S RosenbergCenter for Drug Evaluation and Research, Silver Spring, MD 20993, USA.
Gonçalo Gamboa da CostaDivision of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, AR 72079, USA.
National Center for Toxicological Research · USCenter for Drug Evaluation and Research · US

Funding

Intramural FDA HHS FD999999
6 · The paper itself

Abstract

Polyethylene glycol (PEG) is present in a variety of products. Little is known regarding the accumulation of high-molecular-weight PEGs or the long-term effects resulting from PEG accumulation in certain tissues, especially the choroid plexus. We evaluated the toxicity of high-molecular-weight PEGs administered to Sprague Dawley rats. Groups of 12 rats per sex were administered subcutaneous injections of 20, 40, or 60 kDa PEG or intravenous injections of 60 kDa PEG at 100 mg PEG/kg body weight/injection once a week for 24 weeks. A significant decrease in triglycerides occurred in the 60 kDa PEG groups. PEG treatment led to a molecular-weight-related increase in PEG in plasma and a low level of PEG in cerebrospinal fluid. PEG was excreted in urine and feces, with a molecular-weight-related decrease in the urinary excretion. A higher prevalence of anti-PEG IgM was observed in PEG groups; anti-PEG IgG was not detected. PEG treatment produced a molecular-weight-related increase in vacuolation in the spleen, lymph nodes, lungs, and ovaries/testes, without an inflammatory response. Mast cell infiltration at the application site was noted in all PEG-treated groups. These data indicate that subcutaneous and intravenous exposure to high-molecular-weight PEGs produces anti-PEG IgM antibody responses and tissue vacuolation without inflammation.

Indexed as

AnimalsAntibodiesAntibody FormationChoroid PlexusDisease Models, AnimalDose-Response Relationship, DrugFemaleInjections, IntravenousInjections, SubcutaneousMaleMolecular WeightPolyethylene GlycolsRatsRats, Sprague-DawleyAntibodiesPolyethylene GlycolsAnti-PEG antibodyChoroid plexusPolyethylene glycolVacuolation

Identifiers

PMID35092809
PMCPMC8932377
OpenAlexW4210797093

What OpenQuestion holds

Textmetadata
LicenceTDM
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.