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超高效液相色谱-串联质谱法(UPLC-MS/MS)测定液态食品中焦糖色素的副产物

Determination of caramel colorants' by-products in liquid foods by ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS).

作者信息

Goscinny Séverine, Hanot Vincent, Trabelsi Hasna, Van Loco Joris

机构信息

a Department of Food, Medicines and Consumer Safety , Scientific Institute of Public Health , B-1050 Brussels , Belgium.

出版信息

Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2014;31(10):1652-60. doi: 10.1080/19440049.2014.940609. Epub 2014 Aug 28.

Abstract

2-Methylimidazole, 4-methylimidazole (2-MI and 4-MI), 2-acetyl-4-(1,2,3,4-tetrahydroxybutyl) imidazole (THI) and 5-hydroxymethylfurfural (5-HMF) are neo-formed compounds generated during the manufacture of caramel colours and are transferred to the processed food. These contaminants are known to have a toxicological profile that may pose health risks. Hence, to characterise THI, 2- and 4-MI and 5-HMF levels in liquid foods, an ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed and sample preparation was divided into two analytical strategies depending on the concentration range expected in the type of foods targeted. For the determination of the imidazole substitutes (THI, 2- and 4-MI), a sample enrichment and clean-up step by strong cation solid-phase extraction was developed. This method is capable of quantifying over a range of 5 ng ml⁻¹ (LOQ) to 500 ng ml⁻¹ with recoveries of 75.4-112.4% and RSDs of 1.5-15%. For determination of 5-HMF, a standard addition method was applied covering the linear range of 0.25-30 µg ml⁻¹ with RSDs from 2.8% (for intraday precision) to 9.2% (for intermediate precision). The validated analytical methods were applied to 28 liquid food samples purchased from local markets. THI was found only in the beer samples at levels up to 141.2 ng ml⁻¹. For 2-MI, non-quantifiable traces were observed for all samples, while 4-MI was observed in all samples with large concentration variations (from < LOQ to 563.9 ng ml⁻¹). 5-HMF was found at expected concentrations, except for a sherry vinegar sample (113 µg ml⁻¹), which required a high level of dilution before following the standard addition protocol.

摘要

2-甲基咪唑、4-甲基咪唑(2-MI和4-MI)、2-乙酰基-4-(1,2,3,4-四羟基丁基)咪唑(THI)和5-羟甲基糠醛(5-HMF)是焦糖色素生产过程中产生的新形成化合物,并转移至加工食品中。已知这些污染物具有可能构成健康风险的毒理学特征。因此,为了表征液态食品中THI、2-MI和4-MI以及5-HMF的含量,开发了一种超高效液相色谱-串联质谱法(UPLC-MS/MS),并根据目标食品类型预期的浓度范围将样品制备分为两种分析策略。对于咪唑替代物(THI、2-MI和4-MI)的测定,开发了一种通过强阳离子固相萃取进行样品富集和净化的步骤。该方法能够在5 ng ml⁻¹(定量限)至500 ng ml⁻¹的范围内进行定量,回收率为75.4 - 112.4%,相对标准偏差为1.5 - 15%。对于5-HMF的测定,采用标准加入法,线性范围为0.25 - 30 µg ml⁻¹,相对标准偏差为2.8%(日内精密度)至9.2%(中间精密度)。将经过验证的分析方法应用于从当地市场购买的28个液态食品样品。仅在啤酒样品中发现了THI,含量高达141.2 ng ml⁻¹。对于2-MI,所有样品中均观察到不可定量的痕量,而在所有样品中均观察到4-MI,其浓度变化较大(从低于定量限至563.9 ng ml⁻¹)。除了一个雪利酒醋样品(113 µg ml⁻¹)外,5-HMF的浓度均在预期范围内,该样品在遵循标准加入方案之前需要进行高度稀释。

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