Combination of dispersive solid phase extraction with solidification organic drop-dispersive liquid-liquid microextraction based on deep eutectic solvent for extraction of organophosphorous pesticides from edible oil samples

被引:66
作者
Zahiri, Elham [1 ]
Khandaghi, Jalil [1 ]
Farajzadeh, Mir Ali [2 ,3 ]
Mogaddam, Mohammad Reza Afshar [4 ,5 ]
机构
[1] Islamic Azad Univ, Dept Food Sci & Technol, Sarab Branch, Sarab, Iran
[2] Univ Tabriz, Fac Chem, Dept Analyt Chem, Tabriz, Iran
[3] Near East Univ, Engn Fac, Mersin 10, TR-99138 Nicosia, North Cyprus, Turkey
[4] Tabriz Univ Med Sci, Food & Drug Safety Res Ctr, Tabriz, Iran
[5] Tabriz Univ Med Sci, Pharmaceut Anal Res Ctr, Tabriz, Iran
关键词
Dispersive solid phase extraction; Solidification of floating organic droplet-dispersive liquid-liquid microextraction; Organophosphorous pesticides; Gas chromatography; Nitrogen phosphorous detector; Edible oil; CHROMATOGRAPHY-MASS SPECTROMETRY; GREEN SYNTHESIS STRATEGY; GAS-CHROMATOGRAPHY; CAPILLARY-ELECTROPHORESIS; VEGETABLE-OILS; RESIDUES; INSECTICIDES; EFFICIENT; PRODUCTS; CLEANUP;
D O I
10.1016/j.chroma.2020.461390
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A dispersive solid phase extraction method was combined with deep eutectic solvent-based solidification of floating organic drop-dispersive liquid-liquid microextraction and used for the extraction/preconcentration of some organophosphorus pesticides residues from edible oil samples. The extracted analytes were quantified with gas chromatography-nitrogen phosphorous detector. In this procedure, the sample lipids are saponified with a sodium hydroxide solution and then the analytes are adsorbed onto a primary secondary amine sorbent. After that the analytes are desorbed with acetone as an elution/dispersive solvent and mixed with choline chloride: 3,3-dimethyl butyric acid deep eutectic solvent and the mixture is rapidly dispersed into deionized water. Then, the obtained cloudy solution is centrifuged and placed into an ice bath. The extraction solvent is solidified on the top of the solution. Finally, it is removed and dissolved in acetonitrile, and 1 mu L of the solution is injected into the separation system. Validation of the method showed that limits of detection and quantification were in the ranges of 0.06-0.24 and 0.20-0.56 ng mL(-1), respectively. Enrichment factors and extraction recoveries of the analytes ranged from 170-192 and 68-77%, respectively. The method had an acceptable precision with relative standard deviations less than <= 9.2% for intra-(n=6) and inter-day (n =6) precisions at four concentrations (3, 10, 50, and 250 ng mL(-1), each analyte). Finally the method was used for determination of the analytes in five edible oil samples. (c) 2020 Elsevier B.V. All rights reserved.
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页数:10
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