Biotransformation Potential of Cationic Surfactants in Fish Assessed with Rainbow Trout Liver S9 Fractions

被引:11
作者
Droge, Steven T. J. [1 ]
Armitage, James M. [2 ]
Arnot, Jon A. [3 ]
Fitzsimmons, Patrick N. [4 ]
Nichols, John W. [4 ]
机构
[1] Univ Amsterdam, Inst Biodivers & Ecosyst Dynam, Amsterdam, Netherlands
[2] AES Armitage Environm Sci, Ottawa, ON, Canada
[3] ARC Arnot Res & Consulting, Toronto, ON, Canada
[4] US EPA, Great Lakes Toxicol & Ecol Div, Natl Hlth & Environm Effects Res Lab, Off Res & Dev, Duluth, MN USA
关键词
Biotransformation; Personal care products; Contaminants of emerging concern; In vitro toxicology; Bioaccumulation; Rainbow trout; Liver S9; QUATERNARY AMMONIUM-COMPOUNDS; FREELY DISSOLVED CONCENTRATIONS; XENOBIOTIC INTRINSIC CLEARANCE; IONIZABLE ORGANIC-COMPOUNDS; IN-VITRO; LIQUID-CHROMATOGRAPHY; ONCORHYNCHUS-MYKISS; N-DEMETHYLATION; ALKYLBENZENE SULFONATE; HEPATIC-CLEARANCE;
D O I
10.1002/etc.5189
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Biotransformation may substantially reduce the extent to which organic environmental contaminants accumulate in fish. Presently, however, relatively little is known regarding the biotransformation of ionized chemicals, including cationic surfactants, in aquatic organisms. To address this deficiency, a rainbow trout liver S9 substrate depletion assay (RT-S9) was used to measure in vitro intrinsic clearance rates (CLint; ml min(-1) g liver(-1)) for 22 cationic surfactants that differ with respect to alkyl chain length and degree of methylation on the charged nitrogen atom. None of the quaternary N,N,N-trimethylalkylammonium compounds exhibited significant clearance. Rapid clearance was observed for N,N-dimethylalkylamines, and slower rates of clearance were measured for N-methylalkylamine analogs. Clearance rates for primary alkylamines were generally close to or below detectable levels. For the N-methylalkylamines and N,N-dimethylalkylamines, the highest CLint values were measured for C-10-C-12 homologs; substantially lower clearance rates were observed for homologs containing shorter or longer carbon chains. Based on its cofactor dependency, biotransformation of C-12-N,N-dimethylamine appears to involve one or more cytochrome P450-dependent reaction pathways, and sulfonation. On a molar basis, N-demethylation metabolites accounted for up to 25% of the N,N-dimethylalkylamines removed during the 2-h assay, and up to 55% of the removed N-methylalkylamines. These N-demethylation products possess greater metabolic stability in the RT-S9 assay than the parent structures from which they derive and may contribute to the overall risk of ionizable alkylamines. The results of these studies provide a set of consistently determined CLint values that may be extrapolated to whole trout to inform in silico bioaccumulation assessments. Environ Toxicol Chem 2021;00:1-14. (c) 2021 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.
引用
收藏
页码:3123 / 3136
页数:14
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