Abstract
The sensitive and reliable method for determination of 6 pesticides, cyanazine (triazine), uniconazole (azole), diflufenican (nicotinilide), vernolate (thiocarbamate), bromoxynil (hydroxyl benzonitrile), and asulam (sulfanilyl carbamate) were examined and validated. The methods based on solid-phase extraction (SPE) and gas chromatograph (GC) with electron capture detection (ECD). Confirmation analysis of pesticides was carried out by GC-MS in the selected ion monitoring (SIM) mode using 2 target ions. Method validation was performed at 5 fortification levels (0. 005, 0. 01, 0. 05, 0. 1, and 0. 5 mg/L). The linearity of the calibration curves was excellent in matrix matched standards, and yielded the coefficients of determination (R 2)≥0. 9982 for all target analytes. The limit of quantification (LOQ) was 0. 05 mg/L for 6 pesticide compounds and the reporting level of the method, defined as lower than the maximum residue levels established by Korea Food & Drug Administration (KFDA). Average recoveries of the pesticides spiked at 0. 05, 0. 1, and 0. 5 mg/L into 3 agricultural products, rice, apple, and soybean were in the range 76. 40-120% with relative standard deviation (RSD) values ≤11. 07% for all compounds, respectively.
| Original language | English |
|---|---|
| Pages (from-to) | 1299-1306 |
| Number of pages | 8 |
| Journal | Food Science and Biotechnology |
| Volume | 20 |
| Issue number | 5 |
| DOIs | |
| State | Published - Nov 2011 |
Keywords
- analysis
- GC
- method validation
- pesticide residue
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