Plant-based meat substitute analysis using microextraction with deep eutectic solvent followed by LC-MS/MS to determine acrylamide, 5-hydroxymethylfurfural and furaneol

被引:8
|
作者
Osiecka, Dominika [1 ]
Vakh, Christina [1 ,2 ]
Makos-Chelstowska, Patrycja [3 ]
Kubica, Pawel [1 ]
机构
[1] Gdansk Univ Technol, Fac Chem, Dept Analyt Chem, 11-12 G Narutowicza St, PL-80233 Gdansk, Poland
[2] Gdansk Univ Technol, EcoTech Ctr, 11-12 G Narutowicza St, PL-80233 Gdansk, Poland
[3] Gdansk Univ Technol, Fac Chem, Dept Proc Engn & Chem Technol, 11-12 G Narutowicza St, PL-80233 Gdansk, Poland
关键词
Plant-based meat substitutes; Natural deep eutectic solvent; Acrylamide; 5-Hydroxymethylfurfural; Furaneol; LC-MS/MS; FOOD; IMPACT;
D O I
10.1007/s00216-023-05107-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
For the analysis of plant-based meat substitutes and the determination of Maillard reaction products such as acrylamide, 5-hydroxymethylfurfural and furaneol, a novel and effective procedure based on hydrophobic natural deep eutectic solvent and liquid chromatography coupled with tandem mass spectrometry was developed for the first time. The 49 compositions of the deep eutectic solvents were designed and screened to select the most suitable option. The terpenoids eugenol and thymol in a molar ratio of 2:1 were selected as precursors for solvent formation, allowing effective extraction of the target analytes. The developed procedure comprised two main steps: extraction - in which the analytes are isolated from the solid sample due to the salting-out effect and pre-concentrated in the deep eutectic solvent, and back-extraction - in which the analytes are re-extracted into the formic acid solution for subsequent mass spectrometric detection. As the density of the aqueous phases changed during the extraction and back-extraction steps, the phenomenon of inversion of the coalesced organic phase was observed, which simplified the withdrawing of the phases. The linear range was 1-50 ng/mL for acrylamide, 10-1000 ng/mL for 5-hydroxymethylfurfural and 200-1000 ng/mL for furaneol with coefficients of determination above 0.9952. The developed method was fully validated and found recoveries were in the range 83-120%, with CVs not exceeding 4.9%. The method was applied to real sample analysis of pea-based meat substitutes.
引用
收藏
页码:1033 / 1045
页数:13
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