食品科学

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毛细管电泳法测定糖果及调制酒中10 种人工合成色素

王丽芳1,2,丁晓静1,2,*,解 娜3,赵 珊1,王 志3   

  1. 1.北京市疾病预防控制中心 食物中毒诊断溯源技术北京市重点实验室,北京 100013;
    2.首都医科大学公共卫生学院,北京 100069;3.河北农业大学理学院,河北 保定 071001
  • 出版日期:2014-07-25 发布日期:2014-08-26
  • 通讯作者: 丁晓静
  • 基金资助:

    北京市科技计划项目(Z111100056811006);北京市卫生系统高层次卫生技术人才培养项目

Simultaneous Determination of Ten Synthetic Food Colorants in Alcoholic Beverages and Candies by Capillary Electrophoresis

WANG Li-fang1,2, DING Xiao-jing1,2,*, XIE Na3, ZHAO Shan1, WANG Zhi3   

  1. 1. Beijing Key Laboratory of Diagnostic and Traceability Technologies for Food Poisoning, Beijing Center for Disease Control and
    Prevention, Beijing 100013, China; 2. College of Public Health, Capital Medical University, Beijing 100069, China;
    3. College of Science, Agricultural University of Hebei, Baoding 071001, China
  • Online:2014-07-25 Published:2014-08-26
  • Contact: DING Xiao-jing

摘要:

建立了糖果及调制酒中10 种常用人工合成色素的毛细管电泳-二极管阵列检测新方法。以75 μm×70 cm
(有效长度60 cm)未涂敷石英毛细管为分离柱,25 min内实现了10 种人工合成色素的同时分离与测定。分离电压
18 kV,检测波长为214 nm。研究了影响10 种人工合成色素分离的因素,如分离缓冲溶液的浓度、pH值及添加剂的
浓度等。调制酒样品过膜后直接进样,粉碎后的糖果样品经提取液提取,离心后取上清液直接进样。10 种人工合
成色素的质量浓度分别在1.0~40.0、1.5~60.0、2.0~80.0、3.0~120.0 mg/L范围内与其对应的校正峰面积呈良好线
性关系(r≥0.999 6)。检出限(RSN=3)在0.3~1.0 mg/L之间,定量限(RSN=10)在1.0~3.0 mg/L之间。方法回收
率在92.1%~106.5%之间,相对标准偏差(n=5)在0.5%~4.4%之间。本方法简便、准确,适用于常规实验室中糖
果及调制酒中常用10 种人工合成色素的检测。

关键词: 人工合成色素, 糖果, 调制酒, 毛细管电泳

Abstract:

A new method for the simultaneous determination of ten synthetic food colorants in alcoholic beverages
and candies by capillary electrophoresis (CE) with photodiode array (PDA) detection was established. The
separation was carried out using an uncoated capillary with 75 μm (i.d.) and total length of 70 cm (60 cm to the
detector) within 25 min. The separation voltage was 18 kV. The detection wavelength was set at 214 nm. The
key factors that affect the separation such as the concentration and pH of the running buffer, the concentration
of additives were investigated in detail. The alcoholic beverage was directly injected after filtration. The candy
sample was first ground and then extracted with sample buffer. The extract was centrifuged and the supernatant
could be directly injected. Good linear relationships between the corrected peak areas and mass concentrations
of the ten synthetic food colorants were obtained in the range of 1.0–40.0, 1.5–60.0, 2.0–80.0, 3.0–120.0 mg/L,
respectively, with correlation coefficients all above 0.999 6. The limits of detection (RSN =3) were 0.3–1.0 mg/L,
and the limits of quantitation (RSN =10) were 1.0–3.0 mg/L, respectively. The average recoveries were between 92.1%–
106.5% with relative standard derivations of 0.5%–4.4%. This method is simple and accurate. It can be applied to the routine
analysis of 10 synthetic colorants in alcoholic beverages and candies.

Key words: synthetic colorants, candy, alcoholic beverages, capillary electrophoresis

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