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High-performance liquid chromatographic screening method for mycotoxins using new retention indexes and diode array
Summary
A new reversed-phase high-performance liquid chromatography (RP-HPLC) method efficiently screens for diverse mycotoxins. This method uses novel internal standards for accurate retention index determination, enhancing mycotoxin analysis.
Area of Science:
- Analytical Chemistry
- Food Safety
- Mycology
Background:
- Mycotoxins are toxic secondary metabolites produced by fungi that contaminate food and feed.
- Accurate and efficient methods for mycotoxin detection are crucial for public health and regulatory compliance.
- Existing analytical methods may lack the scope or efficiency for comprehensive mycotoxin screening.
Purpose of the Study:
- To develop and validate a robust reversed-phase high-performance liquid chromatographic (RP-HPLC) screening method for the determination of a wide range of mycotoxins.
- To establish a reliable retention index scale using a novel homologous series of internal standards for improved mycotoxin characterization.
- To demonstrate the applicability of the method for analyzing diverse mycotoxin classes including trichothecenes, aflatoxins, and others.
Main Methods:
- Development of a reversed-phase high-performance liquid chromatographic (RP-HPLC) method utilizing a linear gradient elution with an acetonitrile/water solvent system.
- Characterization of mycotoxins based on retention indexes and on-line UV spectra obtained using a diode array detector (DAD).
- Implementation of a new homologous series of 1-[4-(2,3-dihydroxypropoxy)phenyl]-1-alkanones (D-compounds) as internal standards for the retention index scale.
Main Results:
- The developed RP-HPLC method successfully determined retention indexes for a broad spectrum of mycotoxins with varying polarities and chemical structures.
- The D-compound internal standards provided a reliable basis for the retention index scale, facilitating mycotoxin identification.
- The study included the analysis of multiple trichothecenes (Group A and B), aflatoxins, sterigmatocystin, zearalenone, ochratoxin A, citrinin, and patulin.
Conclusions:
- A versatile RP-HPLC screening method has been established for the simultaneous determination of numerous mycotoxins.
- The use of D-compounds as internal standards enhances the accuracy and reliability of mycotoxin identification via retention indexes.
- This method offers a valuable tool for routine mycotoxin analysis in food safety and quality control.