This application note demonstrates that QuEChERS methodology is well-suited as a sample preparation step prior to GC-MS determination of pesticides in beef tissue. The QuEChERS extraction and subsequent dispersive SPE cleanup steps provide a faster analysis with less toxic reagents, and similar detection limits compared with other methods.
QuEChERS was developed to be quicker, easier, cheaper, safer than, and as rugged as alternative methods of sample preparation. The methodology was developed for analysis of pesticide residues in fruits and vegetables, prior to GC-MS or LC-MS. There are also maximum residue limits (MRLs) for many pesticides in animal products, requiring the determination of pesticide residues in these matrices. Here, we demonstrate the suitability of QuEChERS methodology for determining organophosphorous pesticides in beef muscle tissue. The pesticides chosen have MRLs ranging from 50 to 4000 ppb in beef muscle for US markets.
For a successful analysis using QuEChERS methodology, the sample matrix must be easily homogenized and suitable for extraction with acetonitrile. The sample should contain sufficient water for the liquid partition cleanup, following the addition of the QuEChERS salts. Also, the compound(s) of interest must have a suitable partition co-efficient when partitioned between acetonitrile and salt-saturated water. In this study, a small amount of water was added to the samples to achieve 80% water content. The results of this study indicate that QuEChERS methodology is well-suited as a sample preparation step prior to GC-MS determination of pesticides in beef tissue. The QuEChERS extraction and subsequent dispersive SPE cleanup steps provide a faster analysis with less toxic reagents, and similar detection limits compared with other methods.
Place 10 g of homogenized ground beef into a 50-mL centrifuge tube. Add 2 mL water and 10 mL acetonitrile (ACN), then shake the tube vigorously for 1 min. Add contents of DisQuE pouch salts for CEN QuEChERS (p/n 186006813), and shake vigorously for 1 min. Centrifuge for 3 min at 4000 rpm, and take a 1-mL aliquot of the supernatant (top layer) for dSPE cleanup.
Transfer the 1-mL aliquot of supernatant to a 2-mL dSPE cleanup tube that contains 150 mg of magnesium sulfate, 50 mg PSA sorbent, and 50 mg C18 sorbent (p/n 186004830). Shake vigorously for 1 min. Transfer a portion of the supernatant to the LCMS Certified Vial for GC-MS analysis.
System: |
Agilent 6890 |
Column: |
Rxi-5Sil MS, 30 meter x 0.25 mm (I.D.), 0.25 μm df |
Injection volume: |
1 μL |
Carrier gas: |
Helium |
Flow rate: |
1.0 mL/min (constant flow) |
Temp. program: |
80 °C initial (hold for 1 min), 10 °C/min to 280 °C, and hold for 10 min |
Sample vials: |
LC-MS Certified (p/n 600000751CV) |
Mass spectrometer: |
Waters Quattro micro GC |
The mass spectrometer was operated in positive electron impact (EI+) mode. Data was collected at 70 electron energy (eV) using selected ion monitoring (SIR). The ions monitored consisted of the following, with the principal quantification ion listed first.
Figure 1 shows GC-MS (SIR) chromatograms obtained from analysis of a beef sample spiked at 200 µg/kg (ppb) of each pesticide. Table 1 shows the recovery data. Recovery was calculated by comparing the SIR peak area for samples spiked prior to QuEChERS extraction (pre-spiked samples) with the SIR peak area for samples spiked after QuEChERS extraction (post-spiked samples).
720004456, September 2012