Air-assisted liquid-liquid microextraction of total 3-monochloropropane-1,2-diol from refined edible oils based on a natural deep eutectic solvent and its determination by gas chromatography-mass spectrometry

被引:21
作者
Nemati, Mahboob [1 ,2 ]
Altunay, Nail [3 ]
Tuzen, Mustafa [4 ,5 ]
Farajzadeh, Mir Ali [6 ,7 ]
Nabil, Ali Akbar Alizadeh [1 ]
Lotfipour, Farzaneh [1 ]
Mogaddam, Mohammad Reza Afshar [1 ,8 ]
机构
[1] Tabriz Univ Med Sci, Food & Drug Safety Res Ctr, Tabriz, Iran
[2] Tabriz Univ Med Sci, Fac Pharm, Dept Pharmaceut & Food Control, Tabriz, Iran
[3] Sivas Cumhuriyet Univ, Dept Chem, Sivas, Turkey
[4] Tokat Gaziosmanpasa Univ, Fac Sci & Arts, Chem Dept, TR-60250 Tokat, Turkey
[5] King Fahd Univ Petr & Minerals, Ctr Environm & Water, Res Inst, Dhahran 31261, Saudi Arabia
[6] Univ Tabriz, Fac Chem, Dept Analyt Chem, Tabriz, Iran
[7] Near East Univ, Engn Fac, Mersin 10, TR-99138 Nicosia, North Cyprus, Turkey
[8] Tabriz Univ Med Sci, Pharmaceut Anal Res Ctr, Tabriz, Iran
关键词
Natural deep eutectic solvent; 3-Monochloropropane-1; 2-diol; Edible oil; Gas chromatography; Mass spectrometry; Air-assisted liquid-liquid microextraction; FATTY-ACID ESTERS; SOY-SAUCE; SIMULTANEOUS DERIVATIZATION; PHASE MICROEXTRACTION; 3-CHLOROPROPANE-1,2-DIOL; 3-MCPD; EXTRACTION; PRECONCENTRATION; CHLOROPROPANOLS; GLYCIDOL;
D O I
10.1016/j.chroma.2021.462559
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this paper, a fast, sensitive, and selective sample preparation procedure was presented for the determination of 3-monochloropropane-1,2-diol (3-MCPD) in refined edible oils using gas chromatographymass spectrometry. In this method, firstly, the sample lipids and analyte fatty esters are saponified by sodium hydroxide under sonication. After that the analyte was derivatized using phenylboronic acid (as the derivatization agent) and the obtained derivative was extracted during an air-assisted liquid-liquid microextraction procedure (AALLME). Six different deep eutectic solvents (DESs) were prepared as the extraction solvents and the most effective extraction for 3-MCPD was obtained in the presence of a natural DES (NDES) consisting of choline chloride (ChCl)-acetic acid (AcOH). Important variables such as sodium hydroxide concentration and volume, sonication time, temperature, extraction solvent type and volume, and phenylboronic acid concentration and volume have been optimized. Using the optimum conditions, broad linear range (0.88-1000 ng g(-1)), suitable coefficient of determination (0.995), and low limits of detection (0.26 ng g(-1)) and quantification (0.88 ng g(-1)) were obtained. Relative standard deviations for intra- (n=8) and inter-day (n=6) precisions at a concentration of 5 ng g(-1) were 2.6 and 3.2%, respectively. The developed method has been successfully applied to 3-MCPD determination in refined edible oil samples including sunflower, corn, and canola oils. (C) 2021 Elsevier B.V. All rights reserved.
引用
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页数:11
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