Determination of synthetic dyes in bean and meat products by liquid chromatography with tandem mass spectrometry

被引:23
作者
Li, Juan [1 ,2 ]
Ding, Xiaoming [1 ]
Zheng, Jiaxin [1 ,2 ]
Liu, Dandan [1 ]
Guo, Fei [1 ]
Liu, Hongmin [1 ,2 ]
Zhang, Yanbing [1 ,2 ]
机构
[1] Zhengzhou Univ, Sch Pharmaceut Sci, Zhengzhou 450001, Peoples R China
[2] Zhengzhou Univ, New Drug Res & Dev Ctr, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
Bean products; Liquid chromatography with mass spectrometry; Meat products; Multiresidue analysis; Synthetic dyes; ILLEGAL DYES; SUDAN DYES; CHILI PRODUCTS; ANIMAL FEEDS; DIODE-ARRAY; FOOD DYES; AZO-DYES; HPLC; FOODSTUFFS; SPECTROPHOTOMETRY;
D O I
10.1002/jssc.201400349
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A sensitive and efficient method was developed for the simultaneous determination of eight synthetic dyes (Chrysoidin, Auramine O, Sudan(I-IV), Para Red, and Rhodamine B) in bean and meat products using high-performance liquid chromatography with tandem mass spectrometry. A simple extraction procedure using acetonitrile has been applied for the extraction of these dyes from spiked bean and meat samples. Chromatographic separation was achieved on a Waters XTerra C-18 column (2.1 x 150 mm, 5 m) with a multistep gradient elution. Detection and quantification were performed using mass spectrometry in multiple reaction monitoring mode. Linear calibrations were obtained with correlation coefficients R-2 > 0.99. The limits of detection and quantification for the eight dyes were in the ranges of 0.03-0.75 and 0.1-2.0 g/kg depending on matrices, respectively. The recoveries of these dyes in different food matrices were between 71.2 and 116.9% with relative standard deviations <15.2%, suggesting that the developed method is promising for the accurate quantification of the eight dyes at trace levels in bean and meat products.
引用
收藏
页码:2439 / 2445
页数:7
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