黎俊威,苏君梅,胡 杰,杨 静,陈汉峰,刘春丽.超高效液相色谱法测定食品中枸杞酸含量[J].食品安全质量检测学报,2024,15(24):56-62
超高效液相色谱法测定食品中枸杞酸含量
Determination of ascorbic acid 2-glucoside content in food by ultra performance liquid chromatography
投稿时间:2024-10-28  修订日期:2024-12-01
DOI:
中文关键词:  超高效液相色谱法(UPLC)  枸杞酸  食品
英文关键词:ultra performance liquid chromatography  ascorbic acid 2-glucoside  food
基金项目:
作者单位
黎俊威 1.捷通(广州)检测技术服务有限公司 
苏君梅 1.捷通(广州)检测技术服务有限公司 
胡 杰 1.捷通(广州)检测技术服务有限公司 
杨 静 1.捷通(广州)检测技术服务有限公司 
陈汉峰 1.捷通(广州)检测技术服务有限公司 
刘春丽 1.捷通(广州)检测技术服务有限公司 
AuthorInstitution
LI Jun-Wei 1.Access (Guangzhou) Testing Technology Service Co., Ltd. 
SU Jun-Mei 1.Access (Guangzhou) Testing Technology Service Co., Ltd. 
HU Jie 1.Access (Guangzhou) Testing Technology Service Co., Ltd. 
YANG Jing 1.Access (Guangzhou) Testing Technology Service Co., Ltd. 
CHEN Han-Feng 1.Access (Guangzhou) Testing Technology Service Co., Ltd. 
LIU Chun-Li 1.Access (Guangzhou) Testing Technology Service Co., Ltd. 
摘要点击次数: 44
全文下载次数: 26
中文摘要:
      目的 建立超高效液相色谱法(ultra performance liquid chromatography, UPLC)测定食品中枸杞酸(ascorbic acid 2-glucoside, AA-2βG)含量的分析方法。方法 采用Torus Diol (3.0 mm×100 mm, 1.7 μm)色谱柱, 以乙腈-乙酸铵溶液(85:15, V:V)为流动相进行AA-2βG的分离, 流速为0.4 mL/min, 柱温为40 ℃, 在紫外检测波长260 nm下检测, 外标法定量。结果 AA-2βG在3.01~15.00 μg/mL质量浓度范围内呈现良好的线性关系, 相关系数r2=0.9997, 加标回收率均大于85% (n=9), 相对标准偏差为2.22%, 精密度相对标准偏差为1.33%, 重复性相对标准偏差为1.15%, 本方法的检出限为0.03 μg/g, 定量限为0.09 μg/g。结论 该方法前处理简便, 检测速度快捷、稳定, 灵敏度和准确度高, 可以满足枸杞相关配方产品中AA-2βG的含量测定和质量控制要求, 同时可为行业内对食品中AA-2βG的定性定量分析提供有价值的参考。
英文摘要:
      Objective To establish a method for the determination of ascorbic acid 2-glucoside (AA-2βG) content in food by ultra performance liquid chromatography (UPLC). Methods A Torus Diol (3.0 mm×100 mm, 1.7 μm) column was used, with acetonitrile-ammonium acetate solution (85:15, V:V) as the mobile phase for the separation of AA-2βG, at a flow rate of 0.4 mL/min, column temperature of 40 ℃, and detected at ultraviolet detection wavelength of 260 nm, with external standard quantification. Results The linearity of AA-2βG was good in the range of 3.01–15.00 μg/mL, with a correlation coefficient r2=0.9997. The recovery rates were all greater than 85% (n=9), the relative standard deviation was 2.22%, the relative standard deviation of precision was 1.33%, the relative standard deviation of repeatability was 1.15%, the limit of detection of method was 0.03 μg/g, and the limit of quantification was 0.09 μg/g. Conclusion This method is convenient for pre-treatment, fast in detection speed, stable, and has high sensitivity and accuracy, which can meet the requirements for the determination and quality control of AA-2βG content in related formula products, and can also provide valuable reference for the qualitative and quantitative analysis of AA-2βG in food within the industry.
查看全文  查看/发表评论  下载PDF阅读器