Multi-allergen detection in food by micro high-performance liquid chromatography coupled to a dual cell linear ion trap mass spectrometry
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25042441
DOI
10.1016/j.chroma.2014.06.092
PII: S0021-9673(14)01037-1
Knihovny.cz E-zdroje
- Klíčová slova
- Cookies, Food allergens, Linear ion trap, Mass spectrometry, Multi-allergen analysis,
- MeSH
- alergeny izolace a purifikace MeSH
- analýza potravin metody MeSH
- lidé MeSH
- limita detekce MeSH
- mléčné bílkoviny izolace a purifikace MeSH
- mléko chemie MeSH
- mouka analýza MeSH
- peptidy analýza MeSH
- proteiny ze sójových bobů izolace a purifikace MeSH
- sójové potraviny analýza MeSH
- tandemová hmotnostní spektrometrie metody MeSH
- vaječné proteiny izolace a purifikace MeSH
- vejce analýza MeSH
- vibrace ultrazvukové MeSH
- vysokoúčinná kapalinová chromatografie metody MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- alergeny MeSH
- mléčné bílkoviny MeSH
- peptidy MeSH
- proteiny ze sójových bobů MeSH
- vaječné proteiny MeSH
There is a raising demand for sensitive and high throughput MS based methods for screening purposes especially tailored to the detection of allergen contaminants in different food commodities. A challenging issue is represented by complex food matrices where the antibody-based kits commercially available might encounter objective limitations consequently to epitope masking phenomena due to a multitude of interfering compounds arising from the matrix. The performance of a method duly optimized for the extraction and simultaneous detection of soy, egg and milk allergens in a cookie food matrix by microHPLC-ESI-MS/MS, is herein reported. Thanks to the innovative configuration and the versatility shown by the dual cell linear ion trap MS used, the most intense and reliable peptide markers were first identified by untargeted survey experiment, and subsequently employed to design an ad hoc multi-target SRM method, based on the most intense transitions recorded for each selected precursor peptide. A sample extraction and purification protocol was optimized also including an additional step based on sonication, which resulted in a considerable improvement in the detection of milk allergen peptides. Data Dependent™ Acquisition scheme allowed to fill out a tentative list of potential peptide markers, which were further filtered upon fulfilling specific requirements. A total of eleven peptides were monitored simultaneously for confirmation purposes of each allergenic contaminant and the two most sensitive peptide markers/protein were selected in order to retrieve quantitative information. Relevant LODs were found to range from 0.1μg/g for milk to 0.3μg/g for egg and 2μg/g for soy.
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