College of Agriculture, Hebei University of Engineering, Handan, P. R. China.
Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2010 Sep;27(9):1215-20. doi: 10.1080/19440049.2010.483600.
An analytical method for the simultaneous determination of Sudan dyes (Sudan Red G, Sudan I, Sudan II, Sudan III, Sudan Red 7B and Sudan IV) and Para Red in food by ultra-performance liquid chromatography-electrospray tandem mass spectrometry (UPLC-ESI-MS/MS) was developed. Samples were extracted with acetonitrile, and water added into the extract. The supernatant was analysed by UPLC-MS/MS after refrigeration and centrifugation. The sample was separated on an Acquity BEH C(18) column, and detected by MS/MS with the multiple reaction monitoring mode. Matrix calibration was used for quantitative testing of the method. The linear matrix calibrations of Sudan dyes and Para Red were 2-50 and 10-250 ng g(-1), respectively, and the regression coefficients were >0.9945. The recoveries were 83.4-112.3% with good coefficients of variation of 2.0-10.8%. The limits of detection were between 0.3 and 1.4 ng g(-1) for the six Sudan dyes, and between 3.7 and 6.0 ng g(-1) for Para Red. The limits of quantification were between 0.9 and 4.8 ng g(-1) for the six Sudan dyes, and between 12.2 and 19.8 ng g(-1) for Para Red.
建立了超高效液相色谱-电喷雾串联质谱(UPLC-ESI-MS/MS)同时测定食品中苏丹红染料(苏丹红 G、苏丹红 I、苏丹红 II、苏丹红 III、苏丹红 7B 和苏丹红 4)和对位红的分析方法。样品用乙腈提取,加入水,提取液经冷藏和离心后用 UPLC-MS/MS 分析。样品在 Acquity BEH C(18)柱上分离,采用多反应监测模式的 MS/MS 进行检测。该方法采用基质校准进行定量检测。苏丹红染料和对位红的线性基质校准范围分别为 2-50 和 10-250 ng g(-1),相关系数均大于 0.9945。6 种苏丹红染料的回收率为 83.4-112.3%,变异系数为 2.0-10.8%。6 种苏丹红染料的检测限为 0.3-1.4 ng g(-1),对位红的检测限为 3.7-6.0 ng g(-1)。6 种苏丹红染料的定量限为 0.9-4.8 ng g(-1),对位红的定量限为 12.2-19.8 ng g(-1)。