食品科学 ›› 2011, Vol. 32 ›› Issue (16): 245-248.doi: 10.7506/spkx1002-6630-201116052

• 分析检测 • 上一篇    下一篇

高效液相色谱法测定食品中的安赛蜜

白静   

  1. 北京市通州区产品质量监督检验所
  • 收稿日期:2018-05-21 修回日期:2018-05-21 出版日期:2011-08-25 发布日期:2011-07-26

Determination of Acesulfame K in Food by High Performance Liquid Chromatography

BAI Jing   

  1. (Beijing Tongzhou Institute of Supervision & Testing on Product Quality, Beijing 101100, China)
  • Received:2018-05-21 Revised:2018-05-21 Online:2011-08-25 Published:2011-07-26

摘要: 建立一种高效液相色谱法(high performance liquid chromatography,HPLC)检测食品中人工合成甜味剂安赛蜜的方法。采用C18反相色谱柱,二极管阵列检测器(diode array detector,DAD),以甲醇:0.02mol/L乙酸铵溶液=5.5:94.5(V/V)为流动相,检测波长230nm,流速0.8mL/min,柱温30℃,进样量5μL。安赛蜜出峰时间约在4.6min,样品的检出限为1.7mg/kg,线性范围为1.0~50.0μg/mL,安赛蜜的加标回收率在90%以上,重复性实验的相对标准偏差在2%以下(n=6)。所建立的方法前处理简单,以水为提取溶剂超声波提取安赛蜜,然后在提取液中加入沉淀剂除杂,具有简单、快速、准确、实用性强的特点。

关键词: 安赛蜜, 液相色谱, 测定

Abstract: A high performance liquid chromatography method for the determination of the artificial sweetener acesulfame K in food was developed. Ultrasonic-assisted aqueous extraction followed by the removal of protein impurities by adding zinc acetate and potassium ferrocyanide was used for sample preparation. Acesulfame K was separated on a C18 column using methanol-0.02 mol/L ammonium acetate (5.5:94.5, V/V) as mobile phase at a flow rate of 0.8 mL/min and detected using a diode array detector (DAD) at 230 nm. The column temperature was set at 30 ℃ and the injection volume 5μL. The retention time of acesulfame K was about 4.6 min. The detection limit of the developed method was 1.7 mg/kg, and the linear range was between 1.0 and 50.0μg/mL. The mean spike recoveries for acesulfame K in a blank juice sample exceeded 90%, with a relative standard deviation below 2% (n=6). In this method, acesulfame K was extracted using water as solvent with the assistance of ultrasound, and purified by precipitation. The method proved to be simple, rapid, accurate and practical.

Key words: acesulfame K, high performance liquid chromatography (HPLC), determination

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