Prediction of tissue and urine concentrations of 2-phenoxyethanol and its metabolite 2-phenoxyacetic acid in rat and human after oral and dermal exposures via GastroPlusTM physiologically based pharmacokinetic modelling
Author:
Affiliation:
1. Toxicology and Environmental Research and Consulting, The Dow Chemical Company, Midland, MI, USA
Funder
work featured in this article
Publisher
Informa UK Limited
Subject
Drug Discovery,Molecular Medicine,General Medicine,Bioengineering
Link
https://www.tandfonline.com/doi/pdf/10.1080/1062936X.2022.2049866
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2. 2-Phenoxyethanol [MAK Value Documentation, 2017]
3. Development of a physiologically-based pharmacokinetic model of 2-phenoxyethanol and its metabolite phenoxyacetic acid in rats and humans to address toxicokinetic uncertainty in risk assessment
4. Simultaneous determination of phenoxyethanol and its major metabolite, phenoxyacetic acid, in rat biological matrices by LC–MS/MS with polarity switching: Application to ADME studies
5. Safety review of phenoxyethanol when used as a preservative in cosmetics
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1. Biotransformation and toxicokinetics of 2-phenoxyethanol after oral exposure in humans: a volunteer study;Archives of Toxicology;2024-04-26
2. Predictions of tissue concentrations of myclobutanil, oxyfluorfen, and pronamide in rat and human after oral exposures via GastroPlus TM physiologically based pharmacokinetic modelling;SAR and QSAR in Environmental Research;2024-04-02
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4. Estimated Dermal Penetration of Tetrachlorvinphos (TCVP) in Humans Based on In Silico Modeling and In Vitro and In Vivo Data;Journal of Toxicology and Environmental Health, Part A;2023-05-19
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