Multi-Allergen Quantification in Food Using Concatemer-Based Isotope Dilution Mass Spectrometry: An Interlaboratory Study

Author:

Gavage Maxime1ORCID,Van Vlierberghe Kaatje23ORCID,Dieu Marc45ORCID,Renard Patsy45ORCID,Arnould Thierry45ORCID,Gevaert Kris6789ORCID,De Loose Marc23ORCID,Van Poucke Christof23ORCID,Huet Anne-Catherine1ORCID,Gillard Nathalie1ORCID

Affiliation:

1. CER Groupe , 8 Rue du Point du Jour , 6900 Marloie, Belgium

2. ILVO Flanders Research Institute for Agriculture, Fisheries and Food , , 370 Brusselsesteenweg , 9090 Melle, Belgium

3. Technology and Food Science Unit , , 370 Brusselsesteenweg , 9090 Melle, Belgium

4. University of Namur , , 61 Rue de Bruxelles , 5000 Namur, Belgium

5. Laboratory of Biochemistry and Cell Biology (URBC), Namur Research Institute for Life Sciences (NARILIS) , , 61 Rue de Bruxelles , 5000 Namur, Belgium

6. VIB-UGent , , 75 Technologiepark-Zwijnaarde , 9052 Ghent, Belgium

7. Center for Medical Biotechnology , , 75 Technologiepark-Zwijnaarde , 9052 Ghent, Belgium

8. Ghent University , , 75 Technologiepark-Zwijnaarde , 9052 Ghent, Belgium

9. Department of Biomolecular Medicine , , 75 Technologiepark-Zwijnaarde , 9052 Ghent, Belgium

Abstract

Abstract Background Food allergen analysis is essential for the development of a risk-based approach for allergen management and labeling. MS has become a method of choice for allergen analysis, even if quantification remains challenging. Moreover, harmonization is still lacking between laboratories, while interlaboratory validation of analytical methods is necessary for such harmonization. Objective This interlaboratory study aimed to evaluate the potential of MS for food allergen detection and quantification using a standard addition quantification strategy and a stable isotope-labeled (SIL) concatemer as an internal standard. Methods In-house-produced test material (cookies), blank and incurred with four allergens (egg, milk, peanut, and hazelnut), allergen standards, an internal standard, and the complete methodology (including sample preparation and ultra-HPLC–MS/MS method) were provided to nine laboratories involved in the study. Method sensitivity and selectivity were evaluated with incurred test material and accuracy with spiked test material. Quantification was based on the standard addition strategy using certified reference materials as allergen protein standards and a SIL concatemer as an internal standard. Results All laboratories were able to detect milk, hazelnut, and peanut in the incurred cookies with sufficient sensitivity to reach the AOAC INTERNATIONAL Standard Method Performance Requirements (SMPR® 2016.002). Egg detection was more complicated due to food processing effects, yet five laboratories reached the sensitivity requirements. Recovery results were laboratory-dependent. Some milk and hazelnut peptides were quantified in agreement with SMPR 2016.002 by all participants. Furthermore, over 90% of the received quantification results agreed with SMPR 2016.002 for method precision. Conclusion The encouraging results of this pioneering interlaboratory study represent an additional step towards harmonization among laboratories testing for allergens. Highlights In this pioneering interlaboratory study, food allergens were analyzed by MS with characterized incurred and spiked test materials, calibrated with a certified reference material, and a single SIL concatemer used as an internal standard.

Funder

Belgian Federal Public Service of Health, Food Chain Safety and Environment

Publisher

Oxford University Press (OUP)

Subject

Pharmacology,Agronomy and Crop Science,Environmental Chemistry,Food Science,Analytical Chemistry

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