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Development of a Multi-Toxin UPLC™ MS/MS Method for 50 Mycotoxins and Tropane Alkaloids in Cereal Commodities

Posters | 2022 | Waters | AOACInstrumentation
LC/MS, LC/MS/MS, LC/QQQ
Industries
Food & Agriculture
Manufacturer
Waters

Summary

Significance of the Topic


The reliable detection of mycotoxins and tropane alkaloids in cereal-based commodities is critical for food safety, regulatory compliance, and public health. Advances in ultra-high performance liquid chromatography coupled with tandem mass spectrometry (UPLC-MS/MS) allow simultaneous quantification of multiple toxins at trace levels, streamlining testing workflows and improving analytical throughput.

Objectives and Study Overview


This study extends a previous method to develop a single UPLC-MS/MS assay for over fifty mycotoxins and plant-derived toxins in cereals. Key aims included achieving ultra-low detection limits, stable quantitation in complex grain matrices, and efficient data processing using modern software tools.

Methodology and Instrumentation


Sample Preparation:
  • Homogenize 5 g of cereal flour (wheat, barley, rice, maize).
  • Extract with 20 mL of acetonitrile:water:acetic acid (79:20:1, v/v/v) using automated vortex mixing for 10 min.
  • Centrifuge at >5000 g for 6 min and dilute 150 µL supernatant with 1350 µL water (1:10), yielding a 40× overall dilution.
  • Filter through glass fiber syringe filter prior to analysis.
Solvent and Matrix-Matched Standards:
  • Prepare a stock mix of toxins and perform serial dilutions in water:acetonitrile (95:5, v/v).
  • Matrix-matched calibrants generated by spiking blank cereal extract.
Chromatography and Detection:
  • UPLC separation based on established gradient conditions; void volume ~0.55 min.
  • Detection using Xevo TQ-XS triple quadrupole mass spectrometer in multiple reaction monitoring (MRM) mode with two transitions per analyte.
  • Data processing via MS Quan and waters_connect™ quantitation software.
Used Instrumentation:
  • Waters UPLC system
  • Xevo TQ-XS Mass Spectrometer
  • Oasis PRiME HLB SPE cartridges (optional cleanup)

Main Results and Discussion


Sensitivity and Quantification:
  • Instrument limits of detection (i-LOD) reached as low as 0.0003 ng/mL for aflatoxins B1, B2, G1, G2, and M1.
  • Method limits of quantification (m-LOQ) achieved 0.1 µg/kg for aflatoxins; ≤1 µg/kg for ochratoxin A, sterigmatocystin, beauvericin, enniatins, atropine, scopolamine, and roquefortine C; ≤10 µg/kg for most others, except nivalenol, zearalenone, and penitrem A.
Chromatographic Performance:
  • All analytes (except highly polar moniliformin) exhibited stable retention times (±0.03 min) and clear baseline separation.
  • Calibration curves covered three orders of magnitude with coefficients of determination (R2) >0.99 and residuals <20%.
Moniliformin requires a HILIC approach for confirmation due to its strong polarity and early elution.

Benefits and Practical Applications


This multi-toxin UPLC-MS/MS method offers:
  • Comprehensive screening of regulated, emerging, and masked mycotoxins plus tropane alkaloids in cereals.
  • High sensitivity allowing significant extract dilution and reduction of matrix effects.
  • Streamlined “dilute-and-shoot” sample prep, minimizing labor and consumables.
  • Rapid data review and quantitation via advanced software integration.

Future Trends and Potential Uses


Emerging directions include:
  • Integration of 13C-labelled internal standards to further enhance quantitation accuracy.
  • Automation of sample preparation steps and SPE clean-up to boost throughput.
  • Expansion of the toxin panel to cover additional food matrices and international regulatory portfolios.
  • Implementation of high-resolution MS for non-target screening of unknown mycotoxin metabolites.

Conclusion


The developed UPLC-MS/MS assay on the Xevo TQ-XS platform provides a robust, sensitive, and efficient solution for multi-toxin monitoring in cereal commodities. Its simple sample preparation, low detection limits, and broad analyte scope support routine QA/QC, regulatory compliance, and surveillance of mycotoxin contamination.

Reference


SANTE 12089/2016 guidelines on method validation in the context of pesticide and contaminant analysis.

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