戚美静,杨冀艳,朱昌磊,姚凌峰,洪春苗.高效液相色谱法测定食品中的碱性橙染料[J].食品安全质量检测学报,2016,7(6):2523-2528
高效液相色谱法测定食品中的碱性橙染料
Determination of basic orange dyes in food by high performance liquid chromatography
投稿时间:2015-12-29  修订日期:2016-04-27
DOI:
中文关键词:  高效液相色谱法  碱性橙染料  食品  色素
英文关键词:high performance liquid chromatography  basic orange dyes  food  dyes
基金项目:
作者单位
戚美静 通标标准技术服务天津有限公司 天津 塘沽 
杨冀艳 通标标准技术服务天津有限公司 
朱昌磊 通标标准技术服务青岛分公司 
姚凌峰 通标标准技术服务天津有限公司 
洪春苗 通标标准技术服务天津有限公司 天津 塘沽 
AuthorInstitution
QI Mei-Jing SGS-CSTC Standards Technical Services Tianjin Co Ltd Tanggu Tianjin 
YANG Ji-Yan SGS-CSTC Standards Technical Services Tianjin Co Ltd Tanggu Tianjin 
ZHU Chang-Lei SGS-CSTC Standards Technical Services Co,Ltd Qingdao Branch 
YAO Ling-Feng SGS-CSTC Standards Technical Services Tianjin Co Ltd 
HONG Chun-Miao SGS-CSTC Standards Technical Services Tianjin Co Ltd Tanggu Tianjin 
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中文摘要:
      目的 采用高效液相色谱法测定食品中非法色素添加剂的碱性橙染料即碱性橙2(chrysoidine G, CDG)、碱性橙21(orange G, AOG)及碱性橙22(astrazon orange R, AOR)。方法 样品经乙腈:水:氨水(60:40:0.5, V:V:V)在25 ℃下超声提取30 min, 以0.02 mol/L的乙酸铵溶液(pH为5)和乙腈作为流动相进行梯度洗脱, 采用Agilent XDB C18色谱柱进行分离, 用二极管阵列检测器在449 nm波长处检测CDG, 在485 nm波长处检测AOG及AOR, 以外标峰面积法定量。结果 3种碱性橙染料在0.01~0.2 mg/L浓度范围内线性关系良好, 方法回收率为80.0%~94.0%, 相对标准偏差均小于2%(n=6), 方法的检出限为0.1 mg/kg。结论 本方法操作简便准确, 可适用于腐竹、干辣椒和辣椒油等不同基质样品中碱性橙的检测。
英文摘要:
      Objective To establish a method for determination of 3 kinds of basic orange dyes by high performance liquid chromatography(HPLC), including chrysoidine G (CDG), astrazon orange G (AOG) and astrazon orange R (AOR). Methods Samples were extracted with ultrasonic for 30 min by acetonitrile: water: ammonium hydroxide (60:40:0.5, V:V:V) at 25 ℃. Ammonium acetate (0.02 mol/L, pH=5) and acetonitrile were used as mobile phase for gradient elution, an Agilent XDB C18 column was used for separation, and diode array detector was used for the determination of CDG at 449 nm and AOG and AOR at 485 nm with external standard method for quantification. Results Three kinds of basic orange dyes had good linear relationships in the range of 0.01~0.2 mg/L. The average recoveries were 80%~94% and the relative standard deviations were less than 2% (n=6). The detection limits of the method were 0.1 mg/kg. Conclusion The method is simple and accurate, which is suitable for the determination of basic orange dyes in yuba, dry chili and chili oil.
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