Evidence map›Paper›PMID 35433273›Full record

ArticleToxicology reports2022

Plasma concentrations of tris(1-chloro-2-propyl) phosphate and a metabolite b

Bradley Collins, Desmond Slade, Kristin Aillon, Matthew Stout, Laura Betz, Suramya Waidyanatha, Kristen Ryan

Open access · goldAbstract read
In one paragraph

Article in Toxicology reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 22% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

7 authors at 3 institutions in 1 country.

Bradley CollinsNational Institute of Environmental Health Sciences, Division of the National Toxicology Program, RTP, NC 27709-2233, USA.
Desmond SladeMRIGlobal, Kansas City, MO 64110-2299, USA.
Kristin AillonMRIGlobal, Kansas City, MO 64110-2299, USA.
Matthew StoutNational Institute of Environmental Health Sciences, Division of the National Toxicology Program, RTP, NC 27709-2233, USA.
Laura BetzSocial and Scientific Systems, Inc., Durham, NC 27703, USA.
Suramya WaidyanathaNational Institute of Environmental Health Sciences, Division of the National Toxicology Program, RTP, NC 27709-2233, USA.
Kristen RyanNational Institute of Environmental Health Sciences, Division of the National Toxicology Program, RTP, NC 27709-2233, USA.
National Institute of Environmental Health Sciences · USMRIGlobal · USSocial and Scientific Systems (United States) · US

Funding

Toxicological Assessments for the Division of the National Toxicology ProgramZICES103316 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI WALKER, NIGEL J · 2020 to 2021
$18.5M
Consumer Products and Therapeutics Research ProgramZIAES103379 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI TAYLOR, KYLA · 2022 to 2025
$9.9M
Intramural NIH HHS ZIC ES103316NIEHS NIH HHS HHSN273201400015CNIEHS NIH HHS HHSN273201400020CNIEHS NIH HHS HHSN273201600011C
6 · The paper itself

Abstract

Tris(chloropropyl) phosphate (TCPP) is an organophosphorus flame retardant and plasticizer used in manufacturing and multiple consumer products. Commercial TCPP is a ubiquitous environmental contaminant and TCPP or its metabolites have been detected in human plasma and urine. In response to the demonstrated widespread human exposure and lack of toxicity data, the Division of the National Toxicology Program is investigating the chronic toxicity of TCPP following perinatal exposure in HSD:Sprague Dawley®SD® (HSD) rats (up to 20,000 ppm) and adult exposure in B6C3F1/N mice (females, up to 10,000 ppm; males up to 5000 ppm) to TCPP via feed. Systemic exposure and bioaccumulation were assessed by measuring plasma concentrations of tris(1-chloro-2-propyl)phosphate (TCIPP), the most abundant TCPP isomer. TCIPP concentrations in TCPP-exposed rats and mice ranged from 3.43 to 1180 ng/mL and increased with exposure concentration at all time points. No sex differences were observed in rats, but male mice had higher TCIPP concentrations than females. TCIPP did not bioaccumulate in rats or mice over the course of the study. Low TCIPP concentrations were seen in some control rats and mice that were attributed to background TCPP present during sample collection, preparation and/or analysis. Bis(2-chloroisopropyl) 1-carboxyethyl phosphate (BCPCP), a TCPP metabolite, was quantified in plasma from control and selected exposed animals. Results showed increases in BCPCP concentration that were proportional to exposure concentration in rats and mice at concentrations much higher than TCIPP, indicating that BCPCP might be a more suitable biomarker of TCPP exposure.

Indexed as

B6C3F1/N mouseBCPCP, Bis(2-chloroisopropyl) 1-carboxyethyl phosphateBis(2-chloroisopropyl) 1-carboxyethyl phosphateSprague-Dawley ratSystemic exposureTCIPPTCIPP, Tris(1-chloro-2-propyl)phosphateTCPP, Tris(chloropropyl)phosphateTris(1-chloro-2-propyl)phosphateTris(chloropropyl)phosphate

Identifiers

PMID35433273
PMCPMC9010517
OpenAlexW4221119573

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.