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中国精品科技期刊2020

QuEChERS-HPLC快速测定食品中七种食用合成色素

QuEChERS-HPLC快速测定食品中七种食用合成色素[J]. 食品工业科技, 2013, (12): 81-85. DOI: 10.13386/j.issn1002-0306.2013.12.026
引用本文: QuEChERS-HPLC快速测定食品中七种食用合成色素[J]. 食品工业科技, 2013, (12): 81-85. DOI: 10.13386/j.issn1002-0306.2013.12.026
QuEChERS-high performance liquid chromatography for the determination of synthetic colorants in food[J]. Science and Technology of Food Industry, 2013, (12): 81-85. DOI: 10.13386/j.issn1002-0306.2013.12.026
Citation: QuEChERS-high performance liquid chromatography for the determination of synthetic colorants in food[J]. Science and Technology of Food Industry, 2013, (12): 81-85. DOI: 10.13386/j.issn1002-0306.2013.12.026

QuEChERS-HPLC快速测定食品中七种食用合成色素

基金项目: 

广东省教育部产学研结合项目(2010B090400362); 广东省科技计划项目(2010A032000001-4);

详细信息
  • 中图分类号: TS207.3;O657.72

QuEChERS-high performance liquid chromatography for the determination of synthetic colorants in food

  • 摘要: 建立了一种同时测定豆制品和肉制品中7种食用合成色素(柠檬黄、日落黄、胭脂红、苋菜红、亮蓝、偶氮玉红、诱惑红)的QuEChERS-HPLC方法。样品采用乙醇-氨水-水(7∶2∶1)超声提取,混合使用C18和乙二胺-N-丙基硅烷(PSA)两种基质分散净化剂净化,浓缩后采用SunFireTMC18色谱柱(250mm×4.6mm,5μm)分离。以甲醇-20mmol/L乙酸铵水溶液为流动相,梯度洗脱,流速为1mL/min,测定波长410nm和520nm。实验通过空白基质溶液稀释标准品建立校正的标准曲线,以消除基质效应。结果表明,7种食用合成色素在0.5~10μg/mL线性范围内具有良好的线性关系(相关系数0.9971~0.9999),样品加标回收率为83.01%~108.84%,相对标准偏差为4.53%~15.23%,方法的检出限在0.1~0.3mg/L之间,定量限在0.3~0.4mg/kg之间。方法操作简便、快速、准确,可满足豆制品和肉制品中食用合成色素的分析要求。 
    Abstract: A high performance liquid chromatographic method was developed for the simultaneous determination of 7 synthetic colours such as tartrazine, sunset yellow, ponceau 4R, amaranth, brilliant blue, carmoisine, allura red in bean and meat products. The analytes were extracted from the samples by ethanol-ammonia -water (volume ratio 7∶2∶1) , and purified by a modified QuEChERS (quick, easy, cheap, effective, rigged, and safe) method, and then separated by a SunFire TM C 18 (250mm×4.6mm, 5μm) after concentrating. Methanol-20mmol/L ammonium acetate was used as mobile phase with a gradient elution at the rate of 1mL/min and the detection wavelength was 410nm and 520nm. The interference of matrix was reduced by the matrix-matched calibration standard curves. The linear range was 0.5~10μg/mL with correlation coefficients from 0.9971 to 0.9999. When 0.5~10μg/mL standard solutions were added to blank samples, the average recoveries were 83.01%~108.84% and the relative standard deviations ranged from 4.53% ~15.23% . The limits of detection were ranged from 0.1mg/L to 0.3mg/L and the limit of quantification from 0.3mg/kg to 0.4mg/kg. This method is simple, accurate and sensitive to screen synthetic colorants residue in bean and meat products.
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出版历程
  • 收稿日期:  2013-01-15

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