Concentration dependence of in vitro biotransformation rates of hydrophobic organic sunscreen agents in rainbow trout S9 fractions: Implications for bioaccumulation assessment
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- Leslie J. Saunders
- Department of Biological Sciences Simon Fraser University Burnaby British Columbia Canada
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- Simon Fontanay
- Department of Biological Engineering Polytech Clermont‐Ferrand Clermont‐Ferrand France
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- John W. Nichols
- US Environmental Protection Agency Duluth Minnesota
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- Frank A.P.C. Gobas
- Department of Biological Sciences Simon Fraser University Burnaby British Columbia Canada
説明
<jats:title>Abstract</jats:title><jats:sec><jats:label /><jats:p>In vitro biotransformation studies were performed to support the bioaccumulation assessment of 3 hydrophobic organic ultraviolet filters (UVFs), 4‐methylbenzylidene camphor (4‐MBC), 2‐ethylhexyl‐4‐methoxycinnamate (EHMC), and octocrylene. In vitro depletion rate constants (<jats:italic>k</jats:italic><jats:sub>dep</jats:sub>) were determined for each UVF using rainbow trout liver S9 fractions. Incubations performed with and without added cofactors showed complete (4‐MBC) or partial (EHMC and octocrylene) dependence of <jats:italic>k</jats:italic><jats:sub>dep</jats:sub> on addition of the reduced form of nicotinamide adenine dinucleotide phosphate (NADPH), suggesting that hydrolysis of EHMC and octocrylene by NADPH‐independent enzymes (e.g., carboxylesterases) is an important metabolic route. The concentration dependence of <jats:italic>k</jats:italic><jats:sub>dep</jats:sub> was then evaluated to estimate Michaelis–Menten parameters (<jats:italic>K</jats:italic><jats:sub>M</jats:sub> and <jats:italic>V</jats:italic><jats:sub>max</jats:sub>) for each UVF. Measured <jats:italic>k</jats:italic><jats:sub>dep</jats:sub> values were then extrapolated to apparent whole‐body biotransformation rate constants using an in vitro–in vivo extrapolation (IVIVE) model. Bioconcentration factors (BCFs) calculated from <jats:italic>k</jats:italic><jats:sub>dep</jats:sub> values measured at concentrations well below <jats:italic>K</jats:italic><jats:sub>M</jats:sub> were closer to empirical BCFs than those calculated from <jats:italic>k</jats:italic><jats:sub>dep</jats:sub> measured at higher test concentrations. Modeled BCFs were sensitive to in vitro binding assumptions employed in the IVIVE model, highlighting the need for further characterization of chemical binding effects on hepatic clearance. The results suggest that the tested UVFs are unlikely to accumulate to levels exceeding the European Union Registration, Evaluation, Authorisation, and Restriction regulation criterion for bioaccumulative substances (BCF > 2000 L kg<jats:sup>−1</jats:sup>). However, consideration of appropriate in vitro test concentrations and binding correction factors are important when IVIVE methods are used to refine modeled BCFs. <jats:italic>Environ Toxicol Chem</jats:italic> 2019;38:548–560. © 2018 SETAC</jats:p></jats:sec>
収録刊行物
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- Environmental Toxicology and Chemistry
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Environmental Toxicology and Chemistry 38 (3), 548-560, 2019-02-13
Wiley
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詳細情報 詳細情報について
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- CRID
- 1360016868489141504
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- DOI
- 10.1002/etc.4342
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- ISSN
- 15528618
- 07307268
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- データソース種別
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- Crossref