Suitability of microwave-assisted extraction coupled with solid-phase extraction for organophosphorus pesticide determination in olive oil

被引:45
作者
Fuentes, Edwar [1 ]
Baez, Maria E. [1 ]
Quinones, Adali [1 ]
机构
[1] Univ Chile, Fac Ciencias Quim & Farmaceut, Dept Quim Inorgan & Analit, Santiago, Chile
关键词
Organophosphorus pesticides; Olive oil; Microwave-assisted extraction; Chemometric approach;
D O I
10.1016/j.chroma.2008.08.051
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
A systematic study of the microwave-assisted extraction coupled to solid-phase extraction of nine organophosphorus pesticides (dimethoate, diazinon, pirimiphos methyl, parathion methyl, malathion, fenthion, chlorpyriphos, methidathion and azinphos methyl) from olive oil is described. The method is based on microwave-assisted liquid-liquid extraction with partition of organophosphorus pesticides between an acetonitrile-dichloromethane mixture and oil. Cleanup of extracts was performed with ENVI-Carb solid-phase extraction cartridge using dichloromethane as the elution solvent. The determination of pesticides in the final extracts was carried out by gas chromatography-flame photometric detection and gas chromatography-tandem mass spectrometry, using a triple quadrupole mass analyzer, for confirmative purposes. The study and optimization of the method was achieved through experimental design where recovery of compounds using acetonitrile for partition ranged from 62 to 99%. By adding dichloromethane to the extracting solution, the recoveries of more hydrophobic compounds were significantly increased. Under optimized conditions recoveries of pesticides from oil were equal to or higher than 73%, except for fenthion and chlorpyriphos at concentrations higher than 0.06 mu g g(-1) and diazinon at 0.03 mu g g-1, with RSDs equal to or lower than 11% and quantification limits ranging from 0.007 to 0.020 mu g g(-1). The proposed method was applied to residue determination of the selected pesticides in commercial olive and avocado oil produced in Chile. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:38 / 45
页数:8
相关论文
共 26 条
[1]
Multiresidue method for determination of 35 pesticides in virgin olive oil by using liquid-liquid extraction techniques coupled with solid-phase extraction clean up and gas chromatography with nitrogen phosphorus detection and electron capture detection [J].
Amvrazi, Elpiniki G. ;
Albanis, Triantafyllos A. .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2006, 54 (26) :9642-9651
[2]
Determination of residual pesticides in olive oil by GC-MS and HPLC-MS after extraction by size-exclusion chromatography [J].
Barrek, S ;
Paisse, O ;
Grenier-Loustalot, MF .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2003, 376 (03) :355-359
[3]
Boskou D., 2006, OLIVE OIL CHEM TECHN, P113
[4]
Simplified multiresidue method for the determination of organophosphorus insecticides in olive oil [J].
Cabras, P ;
Angioni, A ;
Melis, M ;
Minelli, EV ;
Pirisi, FM .
JOURNAL OF CHROMATOGRAPHY A, 1997, 761 (1-2) :327-331
[5]
Persistence of insecticide residues in olives and olive oil [J].
Cabras, P ;
Angioni, A ;
Garau, VL ;
Melis, M ;
Pirisi, FM ;
Karim, M ;
Minelli, EV .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1997, 45 (06) :2244-2247
[6]
*COD AL COMM, 1996, COD AL PEST RES FO B, V2
[7]
Diaz Plaza E M, 2007, J CHROMATOGR A, V1174, P145
[8]
Rapid GC-FPD determination of organophosphorus pesticide residues in Sicilian and Apulian olive oil [J].
Dugo, G ;
Di Bella, G ;
La Torre, L ;
Saitta, M .
FOOD CONTROL, 2005, 16 (05) :435-438
[9]
EXPLANATION OF THE MATRIX-INDUCED CHROMATOGRAPHIC RESPONSE ENHANCEMENT OF ORGANOPHOSPHORUS PESTICIDES DURING OPEN-TUBULAR COLUMN GAS-CHROMATOGRAPHY WITH SPLITLESS OR HOT ON-COLUMN INJECTION AND FLAME PHOTOMETRIC DETECTION [J].
ERNEY, DR ;
GILLESPIE, AM ;
GILVYDIS, DM ;
POOLE, CF .
JOURNAL OF CHROMATOGRAPHY, 1993, 638 (01) :57-63
[10]
Determination of pyrethroid insecticide residues in vegetable oils by using combined solid-phases extraction and tandem mass spectrometry detection [J].
Esteve-Turrillas, FA ;
Pastor, A ;
de la Guardia, M .
ANALYTICA CHIMICA ACTA, 2005, 553 (1-2) :50-57