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                  • EI
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                  • 食品科學與工程領域高質量科技期刊分級目錄第一方陣T1
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                  中國精品科技期刊2020
                  龔蕾,韓智,彭青枝,等. 超高效液相色譜-串聯質譜法同時檢測肉制品中17種合成色素的含量[J]. 食品工業科技,2023,44(21):309?315. doi: 10.13386/j.issn1002-0306.2023010014.
                  引用本文: 龔蕾,韓智,彭青枝,等. 超高效液相色譜-串聯質譜法同時檢測肉制品中17種合成色素的含量[J]. 食品工業科技,2023,44(21):309?315. doi: 10.13386/j.issn1002-0306.2023010014.
                  GONG Lei, HAN Zhi, PENG Qingzhi, et al. Determination of 17 Kinds of Synthetic Colorants in Meat Products by UPLC-MS/MS[J]. Science and Technology of Food Industry, 2023, 44(21): 309?315. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023010014.
                  Citation: GONG Lei, HAN Zhi, PENG Qingzhi, et al. Determination of 17 Kinds of Synthetic Colorants in Meat Products by UPLC-MS/MS[J]. Science and Technology of Food Industry, 2023, 44(21): 309?315. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023010014.

                  超高效液相色譜-串聯質譜法同時檢測肉制品中17種合成色素的含量

                  Determination of 17 Kinds of Synthetic Colorants in Meat Products by UPLC-MS/MS

                  • 摘要: 為了建立超高效液相色譜-串聯質譜法(UPLC-MS/MS)同時快速檢測肉制品中17種合成色素的方法。經水振蕩提取樣品,正己烷除油,弱陰離子固相萃取柱(WAX)富集凈化,以乙腈-5 mmol/L乙酸銨為流動相進行梯度洗脫,采取負離子掃描,在多反應監測模式(MRM)下,使17種目標化合物在ACQUITY UPLC HSS T3反相色譜柱上分離,使用外標法定量。結果表明,17種目標化合物在20~1200 μg/L的線性范圍內相關系數均大于0.99,方法的檢出限為0.01~0.05 mg/kg,定量限為0.03~0.15 mg/kg。17種目標化合物在陰性基質中通過添加3個不同加標水平(0.15、0.30和1.0 mg/kg)進行回收率測試,不同水平下的回收率為71.2%~103.5%,相對標準偏差(RSDs,n=6)范圍為1.3%~4.9%。該方法凈化效果好、操作簡單、定量準確,適用于肉制品中合成色素的快速篩查以及快速定量分析。

                     

                    Abstract: To establish a method for the rapid detection of 17 colorants in meat products by ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS), samples were homogeneously extracted with water, degreased with n-hexane, enriched and purified with weak anion solid phase extraction (WAX) column. The seventeen compounds were separated on ACQUITY UPLC HSS T3 column by the gradient elution using acetonitrile-5 mmol/L ammonium acetate solution as mobile phase, detected by MS/MS with negative mode in multiple reaction monitoring (MRM) mode, and finally quantified by external standard method. The correlation coeffcients (r) of the seventeen compounds were above 0.99 in the mass concentration ranging from 20~1200 μg/L. The limits of detection and the limits of quantification of the method were 0.01~0.05 mg/kg and 0.03~0.15 mg/kg, respectively. The recoveries of seventeen analyses spiked at three levels (0.15, 0.30 and 1.0 mg/kg) in meat products ranged from 71.2% to 103.5% with the relative standard deviations (RSDs, n=6) ranged from 1.3%~4.9%. The method was easy to operate and with good purification effect. It could be applied to the rapid determination of the synthetic colorants in meat products .

                     

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