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采用亲水相互作用液相色谱法-质谱联用测定食品基质中几种水溶性维生素(硫胺素、核黄素、烟酰胺和吡哆醇)。

Determination of selected water-soluble vitamins (thiamine, riboflavin, nicotinamide and pyridoxine) from a food matrix using hydrophilic interaction liquid chromatography coupled with mass spectroscopy.

机构信息

Department of Applied Sciences, Faculty of Health and Life Sciences, Ellison Building, Northumbria University, Newcastle Upon Tyne NE1 8ST, United Kingdom.

Department of Applied Sciences, Faculty of Health and Life Sciences, Ellison Building, Northumbria University, Newcastle Upon Tyne NE1 8ST, United Kingdom.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2021 May 1;1171:122541. doi: 10.1016/j.jchromb.2021.122541. Epub 2021 Jan 12.

Abstract

Water-soluble vitamins are essential dietary components with a multitude of important functions that require quantification from food sources to characterise the nutritional status of food. In this study, we have developed a hydrophilic interaction chromatography (HILIC) based method coupled to single-quadrupole mass spectrometry (MS) for the analysis of selected water-soluble vitamins. Due to their involvement in energy release from macronutrients, the quantification of thiamine (B), riboflavin (B), nicotinamide (B) and pyridoxine (B) offers significant value in food analysis. A commercially available vegetable soup was selected as the food matrix for this study and utilised to develop an efficient extraction procedure for the vitamins of interest. Vitamins were extracted using meta-phosphoric acid coupled with a reducing agent, DL-dithiothreitol (DTT) to produce the parent compound. The extracted vitamins were then analysed using an LC-MS system with electrospray - atmospheric pressure ionization (ES-API) source, operated in positive single ion monitoring (SIM) mode. The MS provided good linearity within the investigated range from 5 to 400 ng/mL with coefficient of determination (r) ranging from 0.98 to 0.99. Retention times (0.65-9.04 min) were reproducible and no coelution between vitamins was observed. Limit of detection (LOD) varied from 2.4 to 9.0 ng/mL and limit of quantification (LOQ) was from 8 to 30 ng/mL, comparable to previously published studies. The extraction method provided good intra-day (%CV 1.56-6.56) and inter-day precision (%CV 8.07-10.97). Standard injections were used as part of quality control measures and provided excellent reproducibility (%CV 0.9-3.4). The overall runtime of this method was 19 min, including column reconditioning. Using this method, the quantity of thiamine (67 ± 7 ng/g), riboflavin (423 ± 39 ng/g), nicotinamide (856 ± 77 ng/g) and pyridoxine (133 ± 11 ng/g) was determined from a complex food matrix. In conclusion, we have developed a rapid and reliable, HILIC-single quad MS method utilising SIM for the low-level quantification of four B vitamins in a vegetable soup matrix in under 20 min. This method has shown excellent linearity, intra- and inter-day reproducibility and is directly applicable to other plant-based food matrices.

摘要

水溶性维生素是必需的膳食成分,具有多种重要功能,需要从食物来源中定量分析以表征食物的营养状况。在本研究中,我们开发了一种基于亲水相互作用色谱 (HILIC) 并结合单四极杆质谱 (MS) 的方法,用于分析选定的水溶性维生素。由于它们参与从宏量营养素中释放能量,因此定量分析硫胺素 (B)、核黄素 (B)、烟酰胺 (B) 和吡哆醇 (B) 在食品分析中具有重要价值。本研究选择市售的蔬菜汤作为食品基质,并利用该基质开发了一种有效的感兴趣维生素提取方法。使用偏磷酸和还原剂 DL-二硫苏糖醇 (DTT) 提取维生素,以产生母体化合物。然后使用 LC-MS 系统,采用电喷雾 - 大气压电离 (ES-API) 源,在正单离子监测 (SIM) 模式下分析提取的维生素。MS 在 5 至 400ng/mL 的研究范围内提供了良好的线性度,决定系数 (r) 范围为 0.98 至 0.99。保留时间 (0.65-9.04min) 可重现,且未观察到维生素之间的共洗脱。检测限 (LOD) 范围为 2.4 至 9.0ng/mL,定量限 (LOQ) 范围为 8 至 30ng/mL,与之前的研究结果相当。提取方法提供了良好的日内精密度(%CV 为 1.56-6.56)和日间精密度(%CV 为 8.07-10.97)。标准进样作为质量控制措施的一部分,提供了极好的重现性(%CV 为 0.9-3.4)。该方法的整体运行时间为 19 分钟,包括柱平衡。使用该方法,从复杂的食品基质中确定了硫胺素 (67±7ng/g)、核黄素 (423±39ng/g)、烟酰胺 (856±77ng/g) 和吡哆醇 (133±11ng/g) 的含量。总之,我们开发了一种快速可靠的 HILIC-单四极杆 MS 方法,利用 SIM 在 20 分钟内对蔬菜汤基质中的四种 B 族维生素进行低水平定量分析。该方法具有良好的线性、日内和日间重现性,并且可直接应用于其他植物性食品基质。

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