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气相色谱-串联质谱法同时测定中药中147种农药残留量

Simultaneous Determination of 147 Pesticide Residues in Traditional Chinese Medicines by GC-MS/MS.

作者信息

Ji Chao, Xiao Li, Wang Xingyu, Hua Marti Z, Wu Yifeng, Wang Yifan, Wu Zhiqiang, He Xiahong, Xu Dunming, Zheng Wenjie, Lu Xiaonan

机构信息

Laboratory for Quality Control and Traceability of Food and Agricultural Products, Tianjin Normal University, Tianjin 300387, China.

Department of Food Science and Agricultural Chemistry, McGill University, 21111 Lakeshore Road, Sainte-Anne-de-Bellevue, Quebec H9X 3V9, Canada.

出版信息

ACS Omega. 2023 Jul 26;8(31):28663-28673. doi: 10.1021/acsomega.3c03178. eCollection 2023 Aug 8.

Abstract

Determination of pesticide residues remains a challenge in traditional Chinese medicines in which complex compounds may interfere with analysis signals. This study reports the development of a simple, effective, and high-throughput method combining gas chromatography-tandem mass spectrometry (GC-MS/MS) with either QuEChERS or solid phase extraction (SPE) to determine 147 pesticide residues in traditional Chinese medicines simultaneously. In SPE, the mixture of -hexane and ethyl acetate (1:1, v/v) was selected to extract 147 pesticides in honeysuckle, and the extracted pesticides were determined by GC-MS/MS. The limits of detection for all pesticides were within 0.01-0.05 mg/kg. The recoveries were within 70-120% and the relative standard deviations were below 20% for over 90% pesticides. The coefficients of determination were up to 0.999 for the linearity between MS signals and different concentrations of pesticides (20-200 ng/mL). The analytical performance was confirmed in determining pesticide residues in dried tangerine peel. SPE achieved comparable recoveries for all pesticides compared to the QuEChERS method.

摘要

在中药中,农药残留的测定仍然是一项挑战,因为其中的复杂化合物可能会干扰分析信号。本研究报告了一种简单、有效且高通量的方法,该方法将气相色谱 - 串联质谱法(GC-MS/MS)与QuEChERS或固相萃取(SPE)相结合,以同时测定中药中的147种农药残留。在固相萃取中,选择正己烷和乙酸乙酯的混合物(1:1,v/v)来提取金银花中的147种农药,提取的农药通过GC-MS/MS进行测定。所有农药的检测限在0.01 - 0.05 mg/kg范围内。对于超过90%的农药,回收率在70 - 120%之间,相对标准偏差低于20%。质谱信号与不同浓度农药(20 - 200 ng/mL)之间的线性关系的决定系数高达0.999。在测定陈皮中的农药残留时,证实了该分析性能。与QuEChERS方法相比,固相萃取对所有农药的回收率相当。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb98/10413466/ef65ca8a0f07/ao3c03178_0002.jpg

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