Evidence map›Paper›PMID 26794140›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2016

PBPK Model for Atrazine and Its Chlorotriazine Metabolites in Rat and Human.

Jerry L Campbell, Melvin E Andersen, Paul M Hinderliter, Kun Don Yi, Timothy P Pastoor, Charles B Breckenridge, Harvey J Clewell

Open access · bronzeAbstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.4field-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

12 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Machine learning and artificial intelligence in physiologically based pharmacokinetic modeling.Toxicological sciences : an official journal of the Society of Toxicology · 2023
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. PBPK-Based Probabilistic Risk Assessment for Total Chlorotriazines in Drinking Water.Toxicological sciences : an official journal of the Society of Toxicology · 2016
    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 2 countries.

Jerry L Campbell*The Hamner Institutes for Health Sciences, Center for Human Health Assessment, Research Triangle Park, North Carolina 27709-2137; jcampbell@ramboll.com.
Melvin E Andersen*The Hamner Institutes for Health Sciences, Center for Human Health Assessment, Research Triangle Park, North Carolina 27709-2137;
Paul M HinderliterSyngenta Crop Protection, LLC, Greensboro, North Carolina 27419-8300;
Kun Don YiSyngenta Crop Protection, LLC, Greensboro, North Carolina 27419-8300;
Timothy P PastoorPastoor Science Communications, LLC, Greensboro, North Carolina 27455-3415.
Charles B BreckenridgeSyngenta Crop Protection, LLC, Greensboro, North Carolina 27419-8300;
Harvey J Clewell*The Hamner Institutes for Health Sciences, Center for Human Health Assessment, Research Triangle Park, North Carolina 27709-2137;
The Hamner Institutes for Health Sciences · USSyngenta (Switzerland) · CHSyngenta (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The previously-published physiologically based pharmacokinetic model for atrazine (ATZ), deisopropylatrazine (DIA), deethylatrazine (DEA), and diaminochlorotriazine (DACT), which collectively comprise the total chlorotriazines (TCT) as represented in this study, was modified to allow for scaling to humans. Changes included replacing the fixed dose-dependent oral uptake rates with a method that represented delayed absorption observed in rats administered ATZ as a bolus dose suspended in a methylcellulose vehicle. Rate constants for metabolism of ATZ to DIA and DEA, followed by metabolism of DIA and DEA to DACT were predicted using a compartmental model describing the metabolism of the chlorotriazines by rat and human hepatocytesin vitro Overall, the model successfully predicted both the 4-day plasma time-course data in rats administered ATZ by bolus dose (3, 10, and 50 mg/kg/day) or in the diet (30, 100, or 500 ppm). Simulated continuous daily exposure of a 55-kg adult female to ATZ at a dose of 1.0 µg/kg/day resulted in steady-state urinary concentrations of 0.6, 1.4, 2.5, and 6.0 µg/L for DEA, DIA, DACT, and TCT, respectively. The TCT (ATZ + DEA + DIA + DACT) human urinary biomonitoring equivalent concentration following continuous exposure to ATZ at the chronic point of departure (POD = 1.8 mg/kg/day) was 360.6 μg/L.

Indexed as

Models, BiologicalAbsorption, PhysiologicalAdministration, OralAnimalsAtrazineCells, CulturedDose-Response Relationship, DrugFemaleHepatocytesHumansRats, Sprague-DawleySpecies SpecificityTissue DistributionTriazinesAtrazinechlortriazineTriazinesatrazinechlorotriazinesmetabolism PBPK modelpharmacokineticsrisk assessment.

Identifiers

PMID26794140
PMCPMC4809456
OpenAlexW2307448147

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.