Micellar electrokinetic chromatography in the determination of triazoles in fruit peel

被引:19
作者
Kovac, Ishak [1 ,2 ]
Jakl, Michal [3 ]
Solinova, Veronika [1 ]
Konasova, Renata [1 ]
Kasicka, Vaclav [1 ]
Dytrtova, Jana Jaklova [1 ,4 ]
机构
[1] Czech Acad Sci, Inst Organ Chem & Biochem, Flemingovo Nam 542-2, Prague 16610 6, Czech Republic
[2] Charles Univ Prague, Dept Analyt Chem, Fac Sci, Hlavova 2030, Prague 12843 2, Czech Republic
[3] Czech Univ Life Sci Prague, Fac Agrobiol, Dept Agroenvironm Chem & Plant Nutr, Food & Nat Resources, Kamycka129, Prague 16500, Suchdol, Czech Republic
[4] Charles Univ Prague, Fac Phys Educ & Sport, Dept Physiol & Biochem, Jose Martiho 269-31, Prague 16252 6, Czech Republic
关键词
CD-MEKC; Penconazole; Tebuconazole; Cyproconazole; Triazoles; Tomato peel; CYCLODEXTRIN-MODIFIED MEKC; CAPILLARY-ELECTROPHORESIS; CHIRAL SEPARATION; AROMATASE INHIBITORS; BETA-CYCLODEXTRIN; PESTICIDES; FUNGICIDES; ENANTIOSEPARATION; HEXACONAZOLE; PENCONAZOLE;
D O I
10.1016/j.chroma.2021.462385
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Triazole fungicides (TAFs) are frequently used fungicides for various antifungal treatments of crops. Tre treatment is provided foliarly. However, some significant amount of TAFs may remain on/in fruits. We have developed a methodology for the determination of penconazole, tebuconazole and cyproconazole in tomato fruit peel. The extraction of TAFs was provided with chloroform (acidified with 0.1% acetic acid). In the electrokinetic chromatography, the mixed micellar pseudo-stationary phase was composed of anionic detergent sodium dodecyl sulphate (15 mM) and randomly highly sulphated gamma-cyclodextrin (17.5 mg/mL). The background electrolyte consisted of 100 mM phosphoric acid and 100 mM Tris in the mixed hydro-organic solvent water/methanol (80/20 v/v), apparent pH 4.8. Complete separation of penconazole, tebuconazole, and two diastereomers of cyproconazole with resolutions higher than 5.1 were achieved within a relatively short time of less than 17 min in the bare fused silica capillary of 425/500 mm total/effective lengths and 50/375 mu m I.D./O.D. at separation voltage -15 kV (cathode at injection capillary end) and at constant capillary cassette temperature of 22 degrees C. The TAFs were detected by a UVspectrophotometric diode array detector set at 200 nm. The limits of detection and limits of quantification were in the range of 71-92 and 214-278 mu g/kg of peel, respectively. Analyses of the peel extracts revealed that even 10 days after the last treatment, TAF concentrations were higher than the recommended maximum residue limits in both application ways, as individual as well as in the TAF binary or ternary mixtures. (C) 2021 Elsevier B.V. All rights reserved.
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页数:11
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