Amadori rearrangement products (ARPs) and α-dicarbonyl compounds (α-DCs) are critical intermediates in the Maillard chemistry. The screening of artificially heated honey (AH) is currently based on chromatography-mass spectrometry, which is commonly accompanied with the longer pretreatment and detection time. Here, low-abundance ARPs were detected directly in high-sugar environment by nanoelectrospray ionization mass spectrometry (nanoESI-MS) coupled with borosilicate glass capillaries (O-tips). When O-tips were replaced by borosilicate theta capillaries (θ-tips), the microdroplets allowed the derivatization of α-DCs to be accomplished on the millisecond timescale, rather than hours in conventional protocols. The results indicated that two ARPs and α-DCs of m/z 235 were significantly up-regulated in AH. Meanwhile, the straightforward differentiation between naturally matured honey (NH) and AH was achieved by nanoESI-MS fingerprints combined with multivariate analysis. The method may provide a rapid characterization of Maillard reaction products (MRPs), which exhibits the great application potential in other complex food matrix.
Keywords: 1,4-dideoxyglucosone (PubChem CID: 275366681); 1-deoxyglucosone (PubChem CID: 11228966); 3,4-dideoxyglucoson-3-ene (PubChem CID: 102132119); 3-deoxyglucosone (PubChem CID: 114839); Amadori rearrangement product; Fructose-phenylalanine (PubChem CID: 193670); Fructose-proline (PubChem CID: 119856); Glucosone (PubChem CID: 159630); Honey; Maillard reaction; Nanoelectrospray ionization mass spectrometry; O-phenylenediamine (PubChem CID: 7243); Thermal treatment; l-phenylalanine (PubChem CID: 6140); l-proline (PubChem CID: 145742); α-Dicarbonyl compound.
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