Skip to main content
Log in

In-house validation of a rapid and efficient procedure for simultaneous determination of ergot alkaloids and other mycotoxins in wheat and maize

  • Research Paper
  • Published:
Analytical and Bioanalytical Chemistry Aims and scope Submit manuscript

Abstract

A fundamental step in addressing the global problem of mycotoxins is the development of highly sensitive, multi-class extraction and detection methods. This constitutes a field of research that has in recent years enjoyed a steady advance. Such methods, generally based on liquid chromatography coupled to mass spectrometry, are widely reported successfully detecting various mycotoxins in different food and feed samples. In this work, an innovative approach to multi-class mycotoxin control is proposed, offering specific advantages: a broader inclusion of more mycotoxin classes, robust and thorough extraction for all target compounds despite their varied chemical properties, and determination of all analytes from a single injection. The method involved the extraction and quantification of the main mycotoxins produced by Aspergillus, Fusarium, and Penicillium fungi, as well as their reported derivatives, together with 12 other compounds most commonly produced by Claviceps purpurea. The popularly reported QuEChERS technique has been reduced to a simple “salting-out liquid-liquid extraction” (SO-LLE) to obtain the most efficient extraction of the aforementioned mycotoxin classes in a very short time. This is in particular extremely important in ensuring correct determination of individual ergot alkaloids, for which short and robust sample preparation as well as short analytical sequences were key for minimizing the epimerization during analysis. The analyses of wheat and maize samples were performed using ultra-high performance liquid chromatography coupled with tandem mass spectrometry. Matrix-matched calibration curves were established and limits of quantification were below the maximum levels established by the EU regulation. The precision (repeatability and intermediate precision) was lower than 13% in all cases and recoveries ranged between 60 and 98% in maize and between 62 and 103% in wheat, fulfilling the current legislation. The method was applied to study the co-occurrence of these mycotoxins in wheat (n = 13) and maize (n = 15) samples from six European countries. A successful quantification of 23 different mycotoxins, from all major classes, in 85% of wheat and 93% of maize samples was achieved.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1

Similar content being viewed by others

References

  1. RASFF annual report. 2015. https://ec.europa.eu/food/sites/food/files/safety/docs/rasff_annual_report_2015.pdf. Accessed 10 Nov 2016.

  2. Miller JD. Significance of grain mycotoxins for health and nutrition. In: Champ BR, Highley E, Hocking AD, Pitt JI, editors. Fungi and mycotoxins in stored products. Canberra: ACIAR Proceedings; 1991. p. 126–35.

    Google Scholar 

  3. Smith MC, Madec S, Coton E, Hymery N. Natural co-occurrence of mycotoxins in foods and feeds and their in vitro combined toxicological effects. Toxins. 2016;8:94.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Alassane-Kpembi I, Kolf-Clauw M, Gauthier T, Abrami R, Abiola FA, Oswald IP, et al. New insights into mycotoxin mixtures: the toxicity of low doses of type B trichothecenes on intestinal epithelial cells is synergistic. Toxicol Appl Pharm. 2013;272:191–8.

    Article  CAS  Google Scholar 

  5. Alassane-Kpembi I, Puel O, Oswald IP. Toxicological interactions between the mycotoxins deoxynivalenol, nivalenol and their acetylated derivatives in intestinal epithelial cells. Arch Toxicol. 2015;89:1337–46.

    Article  CAS  PubMed  Google Scholar 

  6. Marroquín-Cardona AG, Johnson NM, Phillips TD, Hayes AW. Mycotoxins in a changing global environment—a review. Food Chem Toxicol. 2014;69:220–30.

    Article  CAS  PubMed  Google Scholar 

  7. Speijers GJ, Speijers MH. Combined toxic effects of mycotoxins. Toxicol Lett. 2004;153:91–8.

    Article  CAS  PubMed  Google Scholar 

  8. Regulation (EC) No. 1881/2006 setting maximum levels for certain contaminants in foodstuffs. Off J Eur Communities 2006;L364:5–24.

  9. Arroyo-Manzanares N, Huertas-Perez JF, Garcia-Campaña AM, Gamiz-Gracia L. Simple methodology for the determination of mycotoxins in pseudocereals, spelt and rice. Food Control. 2014;36:94–101.

    Article  CAS  Google Scholar 

  10. Njumbe Ediage E, Diana Di Mavungu J, Van Peteghem C, De Saeger S. A validated multi-analyte LC–MS/MS method for the quantification of 25 mycotoxins in cassava flour, peanut cake and maize samples. J Agric Food Chem. 2011;59:5173–80.

    Article  CAS  Google Scholar 

  11. Njumbe Ediage E, Van Poucke C, De Saeger S. A multi-analyte LC–MS/MS method for the analysis of 23 mycotoxins in different sorghum varieties: the forgotten sample matrix. Food Chem. 2015;177:397–404.

    Article  CAS  PubMed  Google Scholar 

  12. Al-Taher F, Cappozzo J, Zweigenbaum J, Lee HJ, Jackson L, Ryu D. Detection and quantitation of mycotoxins in infant cereals in the U.S. market by LC-MS/MS using a stable isotope dilution assay. Food Control. 2017;72:27–35.

    Article  CAS  Google Scholar 

  13. Commission Recommendation of 15 March 2012 on the monitoring of the presence of ergot alkaloids in feed and food (2012/154/EU). Off J Eur Communities 2012;L77:20–21.

  14. Zachariasova M, Dzuman Z, Veprikova Z, Hajkova K, Jiru M, Vaclavikova M, et al. Occurrence of multiple mycotoxins in European feeding stuffs, assessment of dietary intake by farm animals. Anim Feed Sci Technol. 2014;193:124–40.

    Article  CAS  Google Scholar 

  15. Malachová A, Sulyok M, Beltrán E, Berthiller F, Krska R. Optimization and validation of a quantitative liquid chromatography–tandem mass spectrometric method covering 295 bacterial and fungal metabolites including all regulated mycotoxins in four model food matrices. J Chromatogr A. 2014;1362:145–56.

    Article  CAS  PubMed  Google Scholar 

  16. Sulyok M, Krska R, Schuhmacher R. A liquid chromatography/tandem mass spectrometric multi-mycotoxin method for the quantification of 87 analytes and its application to semi-quantitative screening of moldy food samples. Anal Bioanal Chem. 2007;389:1505–23.

    Article  CAS  PubMed  Google Scholar 

  17. Diana Di Mavungu J, Malysheva SV, Sanders M, Larionova D, Robbens J, Dubruel P, et al. Development and validation of a new LC–MS/MS method for the simultaneous determination of six major EAs and their corresponding epimers. Application to some food and feed commodities. Food Chem. 2012;135:292–303.

    Article  CAS  Google Scholar 

  18. Commission Decision of 12 August 2002 implementing Council Directive 96/23/EC concerning the performance of analytical methods and the interpretation of results (2002/657/EC). Off J Eur Communities 2002;L221:8–36.

  19. Anastassiades M, Lehotay SJ, Stajnbaher D, Schenck FJ. Fast and easy multiresidue method employing acetonitrile extraction/partitioning and “dispersive solid-phase extraction” for the determination of pesticide residues in produce. J AOAC Int. 2003;86:412–31.

    CAS  PubMed  Google Scholar 

  20. De Boevre M, Diana Di Mavungu J, Maene P, Audenaert K, Deforce D, Haesaert G, et al. Development and validation of an LC-MS/MS method for the simultaneous determination of deoxynivalenol, zearalenone, T-2-toxin and some masked metabolites in different cereals and cereal-derived food. Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2012;29:819–35.

    Article  CAS  PubMed  Google Scholar 

  21. Wenzl T, Haedrich J, Schaechtele A, Robouch P, Stroka J, Guidance document on the estimation of LOD and LOQ for measurements in the field of contaminants in feed and food; EUR 28099, Publications Office of the European Union, Luxembourg, ISBN 978-92-79-61768-3; 2016 https://doi.org/10.2787/8931.

  22. Koesukwiwat U, Sanguankaew K, Leepipatpiboon N. Evaluation of a modified QuEChERS method for analysis of mycotoxins in rice. Food Chem. 2014;153:44–51.

    Article  CAS  PubMed  Google Scholar 

  23. Zhou Q, Li F, Chen L, Jiang D. Quantitative analysis of 10 mycotoxins in wheat flour by ultrahigh performance liquid chromatography-tandem mass spectrometry with a modified QuEChERS strategy. J Food Sci. 2016;81:T2886–90.

    Article  CAS  Google Scholar 

  24. Mohamed R, Gremaud E, Rychoz-Payot J, Tabet J-C, Guy PA. Quantitative determination of five ergot alkaloids in rye flour by liquid chromatography–electrospay ionisation tandem mass spectrometry. J Chromatogr A. 2006;1114:62–72.

    Article  CAS  PubMed  Google Scholar 

  25. Müller C, Kemmlein S, Klaffke H, Krauthause W, Preiß-Weigert A, Wittkowski R. A basic tool for risk assessment: a new method for the analysis of ergot alkaloids in rye and selected rye products. Mol Nutr Food Res. 2009;53:500–7.

    Article  CAS  PubMed  Google Scholar 

  26. Remiro R, Gonzalez-Peñas E, Lizarraga E, Lopez de Cerain A. Quantification of ochratoxin A and five analogs in Navarra red wines. Food Control. 2012;27:139–45.

    Article  CAS  Google Scholar 

  27. Carpio A, Arroyo-Manzanares N, Ríos-Moreno A, Garrido-Jurado I, Gámiz-Gracia L, García-Campaña AM, et al. Development of a QuEChERS-based extraction method for the determination of destruxins in potato plants by UHPLC-MS/MS. Talanta. 2016;146:815–22.

    Article  CAS  PubMed  Google Scholar 

  28. Commission Recommendation of 27 March 2013 on the presence of T-2 and HT-2 toxin in cereals and cereal products (2013/165/EU). Off J Eur Communities 2013;L91:12–15.

  29. Kokkonen MK, Jestoi MN. A multi-compound LC-MS/MS method for the screening of mycotoxins in grains. Food Anal Methods. 2009;2:128–40.

    Article  Google Scholar 

  30. Commission Regulation (EC) No. 401/2006 of laying down the methods of sampling and analysis for the official control of the levels of mycotoxins in foodstuffs. Off J Eur Communities 2006;L70:12–34.

Download references

Acknowledgements

The authors thank the Spanish Ministry of Economy and Competitiveness (Project Ref: AGL2015-70708-R). Natalia Arroyo-Manzanares received a post-doctoral grant from the University of Granada.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to José Diana Di Mavungu.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Additional information

Published in the topical collection Food Safety Analysis with guest editor Steven J. Lehotay.

Electronic supplementary material

ESM 1

(PDF 133 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Arroyo-Manzanares, N., De Ruyck, K., Uka, V. et al. In-house validation of a rapid and efficient procedure for simultaneous determination of ergot alkaloids and other mycotoxins in wheat and maize. Anal Bioanal Chem 410, 5567–5581 (2018). https://doi.org/10.1007/s00216-018-1018-6

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00216-018-1018-6

Keywords

Navigation