色谱

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液相色谱-串联质谱法同时测定不同种类稻米中7种烟酸及衍生物含量

谢满意, 陈铭学, 曹珍珍, 杨欢*   

  1. 中国水稻研究所, 农业农村部稻米及制品检验测试中心, 浙江 杭州 311401
  • 收稿日期:2025-12-05
  • 通讯作者: *E-mail: yanghuan@caas.cn.
  • 基金资助:
    国家水稻产业技术体系(CARS-01); 中央级公益性科研院所基本科研业务费专项(CPSIBRF-CNRRI-202507); 中国农业科学院科技创新工程(ASTIP)

Simultaneous determination of seven nicotinic acid and derivatives contents in different types of rice by liquid chromatography-tandem mass spectrometry

XIE Manyi, CHEN Mingxue, CAO Zhenzhen, YANG Huan*   

  1. Rice Product Quality Inspection Center, Ministry of Agriculture and Rural Affairs, China National Rice Research Institute, Hangzhou 311401, China
  • Received:2025-12-05
  • Supported by:
    National Rice Industrial Technology System (No. CARS-01); Central Public Interest Scientific Institution Basal Research (No. CPSIBRF-CNRRI-202507); the Agricultural Science and Technology Innovation Program (No. ASTIP).

摘要: 烟酸及衍生物作为“全维度抗衰相关关键物质”的重要合成前体,在抗衰、美白和降低慢性疾病发病风险方面具有广阔应用前景。水稻作为全球主要主食之一,被超半数人口消费,其糙米富含烟酸等物质,在天然关键辅酶烟酰胺腺嘌呤二核苷酸(NAD+)前体物的膳食摄入研究中具有重要地位。本研究旨在建立一种可同时分析各类稻米中烟酸及衍生物含量的定量方法,以填补功能稻米产品研发和烟酸及衍生物等天然NAD+前体物监管领域的技术空白。实验比较了提取溶剂、体积和时间等条件对糙米中7种目标化合物提取效率的影响,并优化了吸附材料与净化条件。结果表明,糙米样品采用60%甲醇水溶液(含0.1%甲酸)超声提取20 min,经Oasis HLB固相萃取柱净化,并以乙腈-25 mmol/L碳酸铵溶液梯度洗脱,在XBridgeTM Amide色谱柱(150 mm×2.1 mm, 3.5 μm)上分离,使用多反应监测正离子模式进行检测。实验结果表明,7种烟酸及衍生物在一定浓度范围内线性关系良好,相关系数(r)均大于0.995β0,各物质的检出限为0.001~0.07 mg/kg,定量限为0.004~0.2 mg/kg。7种烟酸及衍生物在籼米、粳米、糯米、红米、紫米和黑米6种稻米基质中的3个加标水平回收率为78.3%~109.8%,相对标准偏差(RSD,n=6)为0.4%~6.7%。将该方法应用于343份稻米样品中7种烟酸及衍生物的含量测定,结果表明7种目标化合物在不同稻米品种间存在显著差异,其中烟酰胺核苷(NR)含量最高,烟酰胺(NAM)最低。本研究建立的方法提取简便,准确度高,重复性好,可实现不同种类稻米中7种烟酸及衍生物的准确定性与定量分析。

关键词: 液相色谱-串联质谱, 固相萃取柱, 烟酸及衍生物, 稻米

Abstract: Nicotinic acid and its derivatives serve as crucial synthetic precursors of "key substances associated with multi-dimensional anti-aging biomarkers". They play significant physiological roles in processes such as anti-aging, skin lightening and reducing the risk of chronic disease. Rice is a major staple food for more than half of the global population. Notably, brown rice contains higher levels of niacin and its related derivatives compared with other foods. Owing to this property, it emerges as a potential candidate for research on the dietary uptake of endogenous nicotinamide adenine dinucleotide (NAD+) precursors. This study aims to establish a quantitative method capable of simultaneously determining the content of nicotinic acid and its derivatives in various types of rice, in order to fill the technical gap in the development of functional rice products and in the regulatory field of natural NAD+ precursors. The effects of extraction solvents, solvent volumes, and extraction time on the extraction efficiencies of the seven target compounds from brown rice were compared. Additionally, the adsorption materials and purification conditions were optimized. The brown rice samples were ultrasonically extracted with 60% methanol aqueous solution (acidified with 0.1% formic acid) for 20 min and purified using an Oasis HLB solid-phase extraction cartridge. Seven target compounds were separated using gradient elution of acetonitrile and 25 mmol/L ammonium carbonate on an XBridgeTM Amide column (150 mm×2.1 mm, 3.5 μm). Detection was carried out in positive ion and multiple reaction monitoring (MRM) modes. The experimental results showed that the seven nicotinic acid and its derivatives exhibited good linearity, with correlation coefficients (r) all greater than 0.995 0. The limits of detection (LODs) and limits of quantification (LOQs) were 0.001-0.07 mg/kg and 0.004-0.2 mg/kg, respectively. The recoveries of the seven target compounds, spiked at three levels in six rice matrices (indica, japonica, glutinous, red, purple, and black rice), ranged from 78.3% to 109.8%, with relative standard deviations (RSDs, n=6) of 0.4%-6.7%. This method was applied to determine the contents of the seven nicotinic acid and its derivatives in 343 rice samples. The results revealed significant differences in the contents of these compounds among different rice varieties. Nicotinamide riboside (NR) was found to be the most abundant derivative among the tested varieties, while nicotinamide (NAM) was the least prevalent consistently. The method established in this study features simple and efficient extraction, high accuracy, and excellent repeatability, thus enabling reliable qualitative and quantitative analysis of the seven nicotinic acid and its derivatives in various rice varieties.

Key words: liquid chromatography-tandem mass spectrometry (LC-MS/MS), solid-phase extraction column, nicotinic acid and its derivatives, rice

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