食品科学 ›› 2020, Vol. 41 ›› Issue (10): 311-316.doi: 10.7506/spkx1002-6630-20190119-232

• 安全检测 • 上一篇    下一篇

QuEChERS-超高效液相色谱-串联质谱法快速测定辣椒红色素中9 种非食用色素

牛瑜琦,马晓斐,李挥,张敬轩,高文惠   

  1. (1.河北科技大学生物科学与工程学院,河北 石家庄 050018;2.河北冠卓检测科技股份有限公司,河北 石家庄 051130;3.河北省医疗器械与药品包装材料检验研究院,河北 石家庄 050061)
  • 出版日期:2020-05-25 发布日期:2020-05-15
  • 基金资助:
    科技部国家国际科技合作专项(2014DFA31220);河北省科技计划项目(16275503D); 石家庄市科学技术研究与发展计划项目(181490372A)

Rapid Determination of Nine Inedible Pigments in Capsanthin by QuEChERS Coupled with Ultra-high Performance Liquid Chromatography-Tandem Mass Spectrometry

NIU Yuqi, MA Xiaofei, LI Hui, ZHANG Jingxuan, GAO Wenhui   

  1. (1. School of Biological Science and Engineering, Hebei University of Science and Technology, Shijiazhuang 050018, China; 2. Hebei Guanzhuo Testing Technology Co. Ltd., Shijiazhuang 051130, China; 3. Hebei Insitute of Medical Equipment and Drugs Packaging Material Inspection, Shijiazhuang 050061, China)
  • Online:2020-05-25 Published:2020-05-15

摘要: 采用QuEChERS前处理方法,结合超高效液相色谱-串联质谱多反应监测模式下的定性和定量分析,实现辣椒红色素中9 种非食用色素的同时检测。辣椒红色素样品经乙腈溶液提取后,氯化钠进行盐析,C18吸附剂净化,取上清液进行超高效液相色谱-串联质谱分析。方法的基质效应影响在-0.17~0.07之间,检出限在0.2~1.5 ng/g之间,定量限在0.6~5.0 ng/g之间,碱性橙II、碱性橙21、碱性橙22、碱性嫩黄在0.2~8 ng/mL范围内线性关系良好,苏丹红I、苏丹红II、苏丹红III、苏丹红IV、罗丹明B在2~40 ng/mL范围内线性关系良好,目标物线性相关系数R2均大于0.995 0,9 种非食用色素在3 个样品加标水平的平均回收率均在69.6%~92.5%之间,相对标准偏差在2.8%~8.5%之间(n=5)。该方法简单快捷、准确可靠,适合于大批量天然植物提取物样品中非食用色素的快速检测。

关键词: 辣椒红色素, QuEChERS, 超高效液相色谱-串联质谱法, 非食用色素, 快速检测

Abstract: A method for simultaneous determination of 9 inedible pigments in capsanthin was developed by a quick, easy, cheap, effective, rugged and safe (QuEChERS) pretreatment method coupled with ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) under the multiple reaction monitoring (MRM) mode. Capsanthin samples were extracted with acetonitrile-water, and then sodium chloride was added for salting out. The extract was cleaned up using C18 sorbent before being analyzed by UPLC-MS/MS. Matrix effect in the method was between ?0.17 and 0.07. The limits of detection (LODs) and limits of quantitation (LOQs) were in the range of 0.2–1.5 ng/g and 0.6–5.0 ng/g, respectively, and good linearity was found in the concentration range of 0.2–8 ng/mL for basic orange II, basic orange 21, basic orange 22 and solvent yellow 34; and of 2–40 ng/mL for sudan I, sudan II, sudan III, sudan IV and rhodamine B chloride with correlation coefficients (R2) higher than 0.995 0. The average recoveries of the 9 inedible pigments at three spiked concentration levels were between 69.6% and 92.5%, with relative standard deviations (RSDs) between 2.8% and 8.5% (n =5). This method proved to be simple, rapid, accurate, reliable, and suitable for the detection of inedible pigments in large quantities of natural plant extract samples.

Key words: capsanthin, QuEChERS, ultra-high performance liquid chromatography-tandem mass spectrometry, inedible pigments, rapid detection

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