Development and Validation of a Quantitative Method for Multiple Allergen Detection in Food Using Concatemer-Based Isotope Dilution Mass Spectrometry

Author:

Gavage Maxime1ORCID,Van Vlierberghe Kaatje2ORCID,Dieu Marc3ORCID,Renard Patsy3ORCID,Arnould Thierry3ORCID,De Loose Marc2ORCID,Gevaert Kris45ORCID,Gillard Nathalie1ORCID,Van Poucke Christof2ORCID

Affiliation:

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

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

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

4. VIB-UGent Center for Medical Biotechnology , Technologiepark-Zwijnaarde 75, 9052 Ghent, Belgium

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

Abstract

Abstract Background Accurate food labeling is essential to protect allergic consumers. However, allergen contaminations may occur during the whole food production process. Reliable, sensitive, and robust methods for detecting multiple allergens in food are needed. Objective This work aims to develop and validate an LC coupled to tandem mass spectrometry (MS/MS) method for the detection and quantification of hazelnuts, peanuts, milk, and eggs in processed food products. Methods In-house-produced incurred test materials, cookies and chocolates, were used for the method development and validation. The quantification was based on the standard addition strategy using qualified reference materials as allergen protein standards and an innovative stable isotope-labeled concatemer as an internal standard. Results A method targeting 19 allergen-specific peptides was developed and validated in two laboratories, which strengthens its robustness. The AOAC INTERNATIONAL performance requirements for repeatability, intermediate precision, reproducibility, and recovery were reached for at least one peptide per allergen across both matrixes, and quantification limits complied with the action levels of the Food Industry Guide to the Voluntary Incidental Trace Allergen Labelling (VITAL®) Program Version 3.0. Conclusion The combination of incurred test materials, standard addition strategy, and stable isotope-labeled concatemer as an internal standard allowed us to develop and validate a robust method for detecting and quantifying multiple allergens in food with sufficient sensitivity to protect allergic consumers. Highlights The combination of characterized incurred test material, calibration with certified reference material, a single stable isotope labelled concatemer and cross-lab validation result in the required standardization and harmonization in food allergen detection according to the stakeholders’ group to assess the robustness of our method.

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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