<span id="5nxvn"><dl id="5nxvn"></dl></span>
<strike id="5nxvn"></strike>
<ruby id="5nxvn"><dl id="5nxvn"></dl></ruby>
<strike id="5nxvn"></strike>
<th id="5nxvn"></th>
<span id="5nxvn"><video id="5nxvn"></video></span>
  • EI
  • Scopus
  • 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
  • DOAJ
  • EBSCO
  • 北大核心期刊
  • 中國核心學術期刊RCCSE
  • JST China
  • FSTA
  • 中國精品科技期刊
  • 中國農業核心期刊
  • CA
  • WJCI
  • 中國科技核心期刊CSTPCD
  • 中國生物醫學SinoMed
中國精品科技期刊2020
戴盡波,沈潔,董文靜,等. 微量QuEChERS-超高效液相色譜-串聯質譜法檢測涼茶中59種非法添加化學藥物[J]. 食品工業科技,2024,45(6):242?253. doi: 10.13386/j.issn1002-0306.2023040213.
引用本文: 戴盡波,沈潔,董文靜,等. 微量QuEChERS-超高效液相色譜-串聯質譜法檢測涼茶中59種非法添加化學藥物[J]. 食品工業科技,2024,45(6):242?253. doi: 10.13386/j.issn1002-0306.2023040213.
DAI Jinbo, SHEN Jie, DONG Wenjing, et al. Determining the 59 Chemical Drugs Illegally Added in Herbal Tea by a Micro-QuEChERS-Based UPLC-MS/MS[J]. Science and Technology of Food Industry, 2024, 45(6): 242?253. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023040213.
Citation: DAI Jinbo, SHEN Jie, DONG Wenjing, et al. Determining the 59 Chemical Drugs Illegally Added in Herbal Tea by a Micro-QuEChERS-Based UPLC-MS/MS[J]. Science and Technology of Food Industry, 2024, 45(6): 242?253. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023040213.

微量QuEChERS-超高效液相色譜-串聯質譜法檢測涼茶中59種非法添加化學藥物

Determining the 59 Chemical Drugs Illegally Added in Herbal Tea by a Micro-QuEChERS-Based UPLC-MS/MS

  • 摘要: 目的:建立一種微量QuEChERS(micro-QuEChERS)結合超高效液相色譜-串聯質譜(UPLC-MS /MS)同時檢測涼茶中59種非法添加藥物的分析方法。方法:樣品用乙腈超聲提取5 min,提取液用NaCl及無水Na2SO4進行鹽析分層,上清液用C18吸附劑進行凈化后,經ACQUITY HSS T3(100 mm×2.1 mm,1.8 μm)色譜柱分離,以0.01%甲酸水溶液(A)-乙腈:甲醇(8:2)(B)為流動相進行梯度洗脫,并采用電噴霧正負離子多反應監測模式檢測,空白基質外標法定量。結果:59種化合物在其線性濃度范圍內,線性關系良好,決定系數均大于0.999,檢出限為5.0~10.0 μg/L,定量限為10.0~25.0 μg/L。在25.0、50.0、100.0 μg/L 3個添加水平下,平均回收率為60.3%~128.8%(n=6),相對標準偏差(RSD)1.0%~13.7%。結論:該方法操作簡單,凈化效果好,靈敏度高,可用于涼茶中59種非法添加化學藥物的快速分析。

     

    Abstract: Objective: An analysis method for simultaneous determination of 59 kinds of chemical drugs illegally added in herbal tea by micro-QuEChERS method combined with ultra performance liquid chromatography-tandem mass spectrometric (UPLC-MS/MS) was established. Method: The samples were extracted by ultrasonic extraction from acetonitrile solution for 5 min and salted out with sodium chloride (NaCl) and anhydrous sodium sulfate (Na2SO4). Supernatant was purified with C18 sorbent and separated on a ACQUITY HSS T3 column (100 mm×2.1mm, 1.8 μm) by gradient elution using a mixture of 0.01% formic acid and acetonitrile:methanol (8:2) as the mobile phase. Then the analytes were quantified by UHPLC-MS/MS in multiple reaction monitoring mode (MRM) via positive and negative electrospray ionization quantified by external standard method. Result: The coefficient of determination of the standard calibration curves for the 59 analytes were all above 0.9990. The limit of detection (LOD, S/N≥3) and the limit of quantitation (LOQ, S/N≥10) were 5.0~10.0 and 10.0~25 μg/L. At three spiked of 25.0, 50.0 and 100.0 μg/L, the average recoveries of 59 analytes were 60.3%~128.8% (n=6) with the relative standard deviations in the range of 1.0%~13.7%. Conclusion: The method developed was simple, sensitive, and had good purification effect. It could be applied for the rapid determination of 59 chemical drugs illegally added in herbal tea.

     

/

返回文章
返回
在线观看国产成人综合视频