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In vitro enantioselective study of the toxicokinetic effects of chiral fungicide tebuconazole in human liver microsomes.

Authors :
Habenschus, Maísa Daniela
Nardini, Viviani
Dias, Luís Gustavo
Rocha, Bruno Alves
Barbosa, Fernando
de Oliveira, Anderson Rodrigo Moraes
Source :
Ecotoxicology & Environmental Safety; Oct2019, Vol. 181, p96-105, 10p
Publication Year :
2019

Abstract

Tebuconazole (TEB) is a chiral triazole fungicide that is globally marketed and used as a racemic mixture to control plant pathogens. Due to its use as a racemic mixture, TEB may exhibit enantioselective toxicokinetics toward nontarget organisms, including humans. Therefore, the in vitro enantioselective metabolism of TEB by cytochrome P450 enzymes (CYP450) was studied using human liver microsomes, and the in vivo toxicokinetic parameters were predicted. A new enantioselective, reversed-phase LC-MS/MS method was developed and validated to analyze the enantiomers of TEB and its main metabolite, 1-hydroxytebuconazole (TEBOH). In vitro metabolic parameters were obtained, and in vitro-in vivo extrapolations were performed. Michaelis-Menten and atypical biphasic kinetic profiles were observed with a total intrinsic clearance ranging from 53 to 19 mL min<superscript>−1</superscript> mg<superscript>−1</superscript>. The in vitro - in vivo extrapolation results showed that TEB first passage effect by the liver seems to be negligible, with hepatic clearance and extraction ratios ranging from 0.53 to 5.0 mL min<superscript>−1</superscript> kg<superscript>−1</superscript> and 2.7–25%, respectively. Preferential metabolism of (+)-TEB to rac -TEB and (−)-TEB was observed, with preferential production of (+)-TEBOH. Furthermore, reaction phenotyping studies revealed that, despite the low hepatic clearance in the first pass metabolism of TEB, multiple human CYP450 isoforms were involved in TEB metabolism when TEBOH enantiomers were generated, mainly CYP3A4 and CYP2C9, which makes TEB accumulation in the human body more difficult due to multiple metabolic pathways. Image 1 • The in vitro enantioselective metabolism of tebuconazole was investigated. • In vivo toxicokinetic parameters were predicted from in vitro data. • Tebuconazole first passage effect by the liver seems to be negligible. • The metabolism showed to be enantioselective. • CYP3A4 and CYP2C9 are the main isoforms involved in tebuconazole metabolism. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01476513
Volume :
181
Database :
Supplemental Index
Journal :
Ecotoxicology & Environmental Safety
Publication Type :
Academic Journal
Accession number :
137249890
Full Text :
https://doi.org/10.1016/j.ecoenv.2019.05.071