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Ochratoxin A in wheat: an intercomparison of procedures
1Royal Veterinary and Agricultural University, Department of Veterinary Microbiology, Friedriksberg C, Denmark.
This study assessed methods for determining ochratoxin A in wheat, finding significant variability. Method improvements, particularly in sample clean-up, are needed for reliable analytical quality control.
Area of Science:
- Food Chemistry
- Analytical Chemistry
- Mycotoxin Analysis
Background:
- Ochratoxin A is a significant food contaminant.
- Accurate analytical methods are crucial for quality control.
- Certified reference materials are needed for method validation.
Purpose of the Study:
- To evaluate methods for ochratoxin A determination in wheat.
- To identify sources of variability in analytical procedures.
- To lay the groundwork for developing certified reference materials.
Main Methods:
- An interlaboratory comparison involving 24 European labs.
- Analysis of naturally contaminated and blank wheat samples.
- Varied extraction solvents (chloroform, methanol, etc.) and clean-up techniques (silica, reversed-phase, immunoaffinity columns).
- High-performance liquid chromatography (HPLC) for determination.
Main Results:
- Recoveries for ochratoxin A ranged widely from 25% to 100%.
- The overall coefficient of variation was 23%.
- Clean-up procedures had a greater impact on result variability than extraction solvents.
- Day-to-day variations and interfering peaks in blank samples were reported.
Conclusions:
- Current methods for ochratoxin A determination in wheat exhibit substantial variability.
- Improvements in clean-up steps are critical for enhancing accuracy and reproducibility.
- Further studies are planned to refine recovery, reproducibility, and investigate matrix effects.
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