冯 鑫,王珮玥,齐鹤鸣,韩 深,别 玮,梁娜娜.高效液相色谱法测定食品中β-阿朴-8’-胡萝卜素醛的含量[J].食品安全质量检测学报,2021,12(2):794-799
高效液相色谱法测定食品中β-阿朴-8’-胡萝卜素醛的含量
Determination of β-apo-8’-carotenal in food by high performance liquid chromatography
投稿时间:2020-09-09  修订日期:2020-12-24
DOI:
中文关键词:  β-阿朴-8’-胡萝卜素醛  高效液相色谱法  食品添加剂  着色剂
英文关键词:β-apo-8’-carotenal  high performance liquid chromatography  food additives  colorants
基金项目:食品安全国家标准制定项目(spaq-2018-042)
作者单位
冯 鑫 中国海关科学技术研究中心 
王珮玥 中国海关科学技术研究中心 
齐鹤鸣 中国海关科学技术研究中心 
韩 深 中国海关科学技术研究中心 
别 玮 中国海关科学技术研究中心 
梁娜娜 中国海关科学技术研究中心, 
AuthorInstitution
FENG Xin Science and Technology Research Center of China Customs 
WANG Pei-Yue Science and Technology Research Center of China Customs 
QI He-Ming Science and Technology Research Center of China Customs 
HAN Shen Science and Technology Research Center of China Customs 
BIE Wei Science and Technology Research Center of China Customs 
LIANG Na-Na Science and Technology Research Center of China Customs 
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中文摘要:
      目的 建立高效液相色谱法测定多种食品中β-阿朴-8’-胡萝卜素醛的含量的方法。方法 样品经20%氢氧化钾40 ℃皂化30 min后, 用正己烷提取, 浓缩蒸干后经Phenomenonex Luna C18色谱柱分离, 以乙腈-水(95:5, V:V)为流动相等度洗脱, 在二极管阵列检测器460 nm条件下检测, 外标法定量。结果 β-阿朴-8’-胡萝卜素醛在0.05~1 μg/mL质量浓度范围内线性关系良好, 相关系数r2>0.999, 检出限为0.0002 g/kg, 回收率为92.3%~97.0%, 相对标准偏差为2.0%~4.7%(n=6)。结论 本方法检出限与定量限均可以满足国家标准中的限量要求, 适用于多种食品中β-阿朴-8’-胡萝卜素醛的含量的检测。
英文摘要:
      Objective To establish a method for the determination of β-apo-8’-carotenal in food by high performance liquid chromatography. Methods The samples were saponified with 20% potassium hydroxide at 40 ℃ for 30 min, then extracted with n-hexane, concentrated and evaporated to dryness, and then separated with Phenomenonex Luna C18 column using acetonitrile-water (95:5, V:V) as mobile phase for isocratic elution, detected by a diode array detector at 460 nm, and quantified by external standard method. Results β-apo-8’-carotenal had a good linear relationship within the mass concentration range of 0.05?1 μg/mL, and the correlation coefficient r2 was more than 0.999. The limit of detection was 0.0002 g/kg, the recoveries were 92.3%?97.0%, and the relative standard deviations were 2.0%?4.7% (n=6). Conclusion The limit of detection and limit of quantification of this method can meet the limit requirements in the national standard, and it is suitable for the detection of β-apo-8’-carotenal content in various foods.
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