Evaluation of chiral triticonazole in three kinds of fruits: enantioseparation, degradation, and dietary risk assessment

Environ Sci Pollut Res Int. 2022 May;29(22):32855-32866. doi: 10.1007/s11356-021-17896-3. Epub 2022 Jan 12.

Abstract

The enantioselective behaviors of chiral pesticides would affect the accuracy of risk assessment. This study evaluated the enantioselectivity of chiral triticonazole (a widely used fungicide) in three kinds of fruits. Firstly, the enantioseparation of triticonazole enantiomers was carried out within 1.2 min utilizing CHIRALPAK OJ-3 column with a mixture of CO2 and methanol (93:7, v/v) using SFC-MS/MS. Secondly, field trials were conducted to clarify the enantioselective degradation and residue of S-( +)-triticonazole and R-(-)-triticonazole in fruits. The initial concentrations of rac-triticonazole were 25.1-93.1 ng/g, and enantioselective degradation was observed in pear, peach, and jujube after 2 h, 10 days, and 3 days, respectively. The degradation of S-( +)-triticonazole was fastest in pear (T1/2, 2.01 days), while the T1/2 of R-(-)-triticonazole was 5.02 days. The residue concentrations of rac-triticonazole were less than the MRL set by EU (10 ng/g) on the 3rd and 21st day in pear and peach, respectively, which were lower than 10 ng/g in jujube on the 30th day (no MRL). Finally, we found that the dietary intake risks of rac-triticonazole in fruits were low for 2-7 age, 20-50 age/female, and 20-50 age/male. The current study could provide complimentary references for the rational usage, MRL formulation, and risk assessment of chiral triticonazole.

Keywords: Chiral triticonazole; Dietary risk assessment; Enantioselective degradation; Enantioseparation; Fruits; SFC-MS/MS.

MeSH terms

  • Cyclopentanes
  • Fruit* / chemistry
  • Fungicides, Industrial* / analysis
  • Risk Assessment
  • Stereoisomerism
  • Tandem Mass Spectrometry
  • Triazoles / analysis

Substances

  • Cyclopentanes
  • Fungicides, Industrial
  • Triazoles
  • triticonazole