任丹丹,谢云峰,刘佳佳,杨永坛,李月琪.高效液相色谱法同时测定食品中9种水溶性维生素[J].食品安全质量检测学报,2014,5(3):899-904
高效液相色谱法同时测定食品中9种水溶性维生素
Simultaneous determination of nine water-soluble vitamins in foods by high performance liquid chromatography
投稿时间:2014-01-18  修订日期:2014-03-17
DOI:
中文关键词:  高效液相色谱法  水溶性维生素  食品
英文关键词:high performance liquid chromatography  water-soluble vitamins  foods.
基金项目:中粮集团有限公司年度科技计划项目(2013-C2-F001L)
作者单位
任丹丹 中粮营养健康研究院;北京市营养健康与食品安全重点实验室 
谢云峰 中粮营养健康研究院;北京市营养健康与食品安全重点实验室 
刘佳佳 中粮营养健康研究院;北京市营养健康与食品安全重点实验室 
杨永坛 中粮营养健康研究院;北京市营养健康与食品安全重点实验室 
李月琪 岛津国际贸易有限公司北京分析中心 
AuthorInstitution
REN Dan-Dan COFCO Nutrition and Health Research Institute;Beijing Key Laboratory of Nutrition Health and Food Safety 
XIE Yun-Feng COFCO Nutrition and Health Research Institute;Beijing Key Laboratory of Nutrition Health and Food Safety 
LIU Jia-Jia COFCO Nutrition and Health Research Institute;Beijing Key Laboratory of Nutrition Health and Food Safety 
YANG Yong-Tan COFCO Nutrition and Health Research Institute;Beijing Key Laboratory of Nutrition Health and Food Safety 
LI Yue-Qi Department of Analytical Instruments, Shimadzu International Trading (Shanghai) Co., Ltd. 
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中文摘要:
      目的建立同时测定食品中9 种水溶性维生素的高效液相色谱分析方法。方法采用 C18 色谱柱进行分离, 以pH 2.5, 25 mmol/L KH2PO4-乙腈二元体系为流动相进行梯度洗脱, 最后用高效液相色谱二极管阵列检测器对9 种维生素进行测定。结果在优化实验条件下, 测得维生素C 的线性范围为0.04~100 μg/mL, 硫胺、核黄素、烟酰胺和吡哆醇的线性范围为0.02~100 μg/mL, 泛酸的线性范围为0.08~400 μg/mL, 生物素的线性范围为0.08~200 μg/mL, 叶酸的线性范围为0.01~50 μg/mL, 氰钴胺的线性范围为0.04~100 μg/mL; 线性相关系数为0.9997~0.9999, 相对标准偏差为0.28%~1.35%, 检出限范围为3~45 ng/mL, 加标回收率为90.6%~105.4%。结论 该方法快速、准确、灵敏, 适合测定营养强化食品中多种水溶性维生素。
英文摘要:
      Objective To develop a high performance liquid chromatography (HPLC) method for the determination of nine water-soluble vitamins in foods. Methods The chromatographic separation was performed on a C18 column with gradient elution, using potassium dihydrogen phosphate and acetonitrile as mobile phase. The analyte was detected by HPLC with diode array detector. Results Under the optimal conditions, the calibration curves of nine vitamins were linear in the range of 0.04~100 μg/mL for vitamin C, 0.02~100 μg/mL for thiamine, riboflavin, nicotinamide and pyridoxine; 0.08~400 μg/mL for pantothenic acid; 0.08~200 μg/mL for biotin; 0.01~50 μg/mL for folic acid; and 0.04~100 μg/mL for cyanocobalamin with correlation coefficient (r) more than 0.9997. The relative standard deviations (RSDs) were less than 1.35%, and the limit of detection (LOD) was found in the range of 3~45 ng/mL and the spiked recoveries were between 90.6~105.4%. The developed method was applied to determine the water-soluble vitamins in functional beverages, multivitamin tablets and fortified rice. Conclusion The proposed method is rapid, accurate and sensitive, and it is suitable for detecting water-soluble vitamins in fortified foods.
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