湖北农业科学 ›› 2024, Vol. 63 ›› Issue (7): 171-175.doi: 10.14088/j.cnki.issn0439-8114.2024.07.028

• 检测分析 • 上一篇    下一篇

高效液相色谱法同时测定果蔬中有机酸和维生素C含量

李红艳, 李丽梅, 钱训, 张嘉坤, 郑振山, 陈勇达   

  1. 河北省农林科学院生物技术与食品科学研究所,石家庄 050051
  • 收稿日期:2023-07-31 出版日期:2024-07-25 发布日期:2024-07-24
  • 通讯作者: 陈勇达(1975-),男,河北石家庄人,副研究员,主要从事农药残留分析和农产品质量安全研究,(电子信箱)yongdachen@126.com。
  • 作者简介:李红艳(1981-),女,河北石家庄人,助理研究员,主要从事农产品质量安全研究,(电话)13630816338(电子信箱)57946481@qq.com
  • 基金资助:
    河北省重点研发计划项目(21326803D); 河北省农林科学院科技创新专项课题(2022KJCXZX-SSS-7)

Simultaneous determination of organic acids and VC content in fruits and vegetables using high performance liquid chromatography

LI Hong-yan, LI Li-mei, QIAN Xun, ZHANG Jia-kun, ZHENG Zhen-shan, CHEN Yong-da   

  1. Institute of Biotechnology and Food Science, Hebei Academy of Agriculture and Forestry Sciences, Shijiazhuang 050051, China
  • Received:2023-07-31 Published:2024-07-25 Online:2024-07-24

摘要: 采用1%草酸(含10%甲醇)溶液提取果蔬的有机酸(酒石酸、柠檬酸、苹果酸、丁二酸、反丁烯二酸)和维生素C,色谱柱为InertSustain C18(250 mm×4.6 mm,5 μm),流动相A为0.1%磷酸水溶液,流动相B为甲醇,梯度洗脱,进样体积为20 μL,柱温为30 ℃,流速为0.8 mL/min,在210 nm和254 nm波长处分别检测5种有机酸和维生素C的含量。结果表明,该方法在标准曲线范围内线性关系良好,相关系数(R2)均大于0.999 0,检出限为0.01~0.90 μg/mL,定量限为0.15~5.00 μg/mL,方法的相对标准偏差为2.40%~3.75%,回收率在86.4%~115.2%;该方法具有分析速度快、灵敏度高、重复性好、效率高等优点,可用于果蔬中有机酸和维生素C的含量测定。

关键词: 高效液相色谱法, 果蔬, 有机酸, 维生素C, 含量

Abstract: Using a 1% oxalic acid (containing 10% methanol) solution to extract organic acids (tartaric acid, citric acid, malic acid, succinic acid, fumaric acid) and VC from fruits and vegetables,the chromatographic column was InertSustain C18 (250 mm×4.6 mm, 5 μm), with 0.1% phosphoric acid aqueous solution as mobile phase A and methanol as mobile phase B, gradient elution, injection volume of 20 μL, column temperature of 30 ℃, and flow rate of 0.8 mL/min. The content of 5 organic acids and was detected VC at wavelengths of 210 nm and 254 nm, respectively. The results showed that the method had a good linear relationship within the standard curve range, with correlation coefficients (R2) all greater than 0.999 0, detection limits of 0.01~0.90 μg/mL, quantification limits of 0.15~5.00 μg/mL, relative standard deviation of 2.40%~3.75%, and recovery rates of 86.4%~115.2%;this method had the advantages of fast analysis speed, high sensitivity, good repeatability, and high efficiency, and could be used for the determination of organic acids and VC content in fruits and vegetables.

Key words: high performance liquid chromatography, fruits and vegetables, organic acids, VC, content

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