吕 卓,李 涛,贺 茜,史朝烨,雷会宁,樊少娟,马 月,乔蓉霞.高效液相色谱法测定保健食品中的羟基酪醇[J].食品安全质量检测学报,2020,11(19):6781-6786
高效液相色谱法测定保健食品中的羟基酪醇
Determination of hydroxytyrosol in health food by high performance liquid chromatography
投稿时间:2020-07-23  修订日期:2020-09-23
DOI:
中文关键词:  保健食品  羟基酪醇  高效液相色谱法
英文关键词:health food  hydroxytyrosol  high performance liquid chromatography
基金项目:食品安全风险物质筛查检测服务平台建设(2019PT-22)
作者单位
吕 卓 陕西省食品药品监督检验研究院 
李 涛 陕西省食品药品监督检验研究院 
贺 茜 陕西省食品药品监督检验研究院 
史朝烨 陕西省食品药品监督检验研究院 
雷会宁 陕西省食品药品监督检验研究院 
樊少娟 陕西省食品药品监督检验研究院 
马 月 陕西省食品药品监督检验研究院 
乔蓉霞 陕西省食品药品监督检验研究院 
AuthorInstitution
LV Zhuo Shaanxi Institute for Food and Drug Control 
LI Tao Shaanxi Institute for Food and Drug Control 
HE Qian Shaanxi Institute for Food and Drug Control 
SHI Zhao-Ye Shaanxi Institute for Food and Drug Control 
LEI Hui-Ning Shaanxi Institute for Food and Drug Control 
FAN Shao-Juan Shaanxi Institute for Food and Drug Control 
MA Yue Shaanxi Institute for Food and Drug Control 
QIAO Rong-Xia Shaanxi Institute for Food and Drug Control 
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中文摘要:
      目的 建立高效液相色谱法测定保健食品中羟基酪醇的方法。方法 样品用二甲基亚砜进行超声提取后, 采用Waters Spherisorb ODS2色谱柱(250 mm×4.6 mm, 5 μm)进行分离, 以0.12%甲酸水溶液?0.12%甲酸甲醇溶液为流动相等度洗脱, 柱温为30 ℃, 流速1 mL/min, 紫外检测器进行检测, 外标法定量。结果 羟基酪醇在12.45~498.0 μg/mL范围内线性关系良好, 相关系数大于0.999; 检出限为0.03 g/100 g; 定量限为 0.12 g/100 g; 平均回收率为99.5%~100.6%, 相对标准偏差值为0.55%~1.13%。结论 该方法简便、快捷、高效、准确, 适用于保健食品中羟基酪醇的测定。
英文摘要:
      Objective To establish a method for the determination of hydroxytyrosol in health food by high performance liquid chromatography. Methods After ultrasonic extraction with dimethyl sulfoxide, the samples were separated with Waters Spherisorb ODS2 column (250 mm×4.6 mm, 5 μm) by using 0.12% formic acid aqueous solution-0.12% formic acid methanol solution as mobile phase for isocratic elution at the flow of 1 mL/min. The temperature of column was 30 ℃. The samples were detected by UV detector and quantified by external standard method. Results Hydroxytyrosol had a good linear relationship in the range of 12.45?498.0 μg/mL, and the correlation coefficient was greater than 0.999. The limit of detection was 0.03 g/100 g. The limit of quantitation was 0.12 g/100 g. The average recoveries were 99.5%?100.6%, and the relative standard deviations were 0.55%?1.13%. Conclusion This method is simple, rapid, efficient and accurate, which can be applied to detect hydroxytyrosol in health food.
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