The pesticide formulations were obtained from local licensed markets. A simple multiresidue method was employed to detect the selected pesticides (chlorinated hydrocarbon, organophosphate, carbamates, and pyrethroid insecticide) according to Kadenczki et al. (
18) and Abbassy (
19). The principles of the abovementioned method were based on a homogenous sample pulp adsorbed on the surface of activated florisil to obtain a free-flowing powder. For this purpose, a 5-g of homogenous sample was extracted into a glass column with 5 mL ethyl acetate. Gas chromatography (GC) was used as follows:
(1) Shimadzu GC 17A series equipped with electron capture detector (ECD) interfaced to HP5 fused silica column, 30 m × 0.53 mm id, the 2.65 µm film thickness (Hewlett), to detect organochlorine and pyrethroid pesticides.
(2) Shimadzu GC 17A series equipped with nitrogen phosphorus detector (NPD), interfaced to HP190915 - 433 column, 30 m × 0.25 mm id, 0.25 µm film thickness, to detect organophosphorus insecticide and nitrogen containing pesticides.
(3) GC/MS HP6890 series equipped with mass spectrometer detector (MSD), interfaced to HP-5MS capillary column, and split/splitless injection mode. Helium was used as a carrier gas.
(4) Operating condition for GC/ECD: Injector temperature 250°C, detector temperature 300°C, oven temperature initially 100°C, 1st ramp: 25°C/minute up to 180°C (one minute hold), 2nd ramp: 10°C/minute up to 220°C (one minute hold), 3rd ramp: 5°C/minute up to 300°C, final temperature 300°C (five minutes hold).
(5) Operating condition for GC/NPD: Injector temperature 200°C, detector temperature 280°C, column temperature increased from 90°C to 210°C at 20°C/minute (on hold) and increased to 280°C at 5°C/minute (10 minutes hold).
(6) Operating condition for GC/MS: Injector temperature 200°C, initial temperature 160°C (three minutes hold), 1st ramp 25°C/minute to 210°C (one minute hold), 2nd ramp 10°C/minute to 260°C, final temperature 260°C (five minutes hold).
Solvents and reagents such as acetone, ethyl acetate, methylene chloride, methanol, ethanol, n-hexane and florisil 60 - 100 mesh, and sodium sulfides were of analytical reagent grade. Analytical standards of the pesticides were provided by Accustandard Europe Niederbipp, Switzerland.
The analytical standards were as follows:
(a) Endosulfan as a chlorinated hydrocarbon insecticide,
(b) Diazinon, dichlorvos, and chlorpyrifos as an organophosphorus pesticide,
(c) Carbaryl as a carbamate insecticide,
(d) Fenpropathrin and permethrin as a halogenated pyrethroid insecticide.
Quality control of the analysis of pesticide residues (cucumber and tomato) consists of (1) analysis of blank samples; (2) analysis of the samples in duplicate; (3) determination of the method detection limits for the analyzed pesticides using samples with no pesticide residue (the limits of the obtained detection method ranged 0.5 to 2.0 ppb to detect the GC of the tested pesticides, and < 0.1 ppm for the GC/MS system); (4) estimation of the extraction procedure efficiency (recovery test), pulp samples of the fresh tomatoes and cucumbers were fortified at 0.5 and 1 mg/kg of the analytical standards dissolved in acetone. Recoveries of all pesticides were tested in five replicates. The obtained recovery of the analyzed pesticides ranged from 81.16 to 103.3 (5). The simultaneous injection of the samples was performed with two different systems and the obtained data were considered in case of similarity.