Determination of anthraquinone in tea by stable isotope dilution assay-gas chromatography-tandem mass spectrometry

被引:1
作者
Xie, Wen [1 ]
Huang, Chaoqun [1 ]
Hong, Deng [1 ]
Hou, Jianbo [1 ]
Deng, Xiaojun [2 ]
Han, Chao [3 ]
机构
[1] Zhejiang Acad Sci & Technol Inspect & Quarantine, Hangzhou 310016, Zhejiang, Peoples R China
[2] Tech Ctr Anim Plant & Food Inspect & Quarantine S, Shanghai 200135, Peoples R China
[3] Zhejiang Shuren Univ, Coll Biol & Environm Engn, Hangzhou 310015, Zhejiang, Peoples R China
来源
SN APPLIED SCIENCES | 2020年 / 2卷 / 06期
关键词
Anthraquinone residue; Tea; Stable isotope dilution assay; GC-MS/MS; PERFORMANCE LIQUID-CHROMATOGRAPHY; SOLID-PHASE EXTRACTION; GALLIC ACID; PESTICIDES; IDENTIFICATION; IONIZATION; RESIDUES; L;
D O I
10.1007/s42452-020-2919-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The aim of this study was to develop an analytical method for the accurate determination of the anthraquinone residue in tea samples (Pu'er tea, oolong tea, green tea, and black tea) by stable isotope dilution assay-gas chromatography-tandem mass spectrometry (SIDA-GC-MS/MS). Samples were purified by solid-phase extraction after extraction with n-hexane:acetone (1:1, v/v). The anthraquinone residue was then detected by selected reaction monitoring (SRM) in electron ionization mode. Anthraquinone-d8 was added in the tea sample extraction process to eliminate the matrix effect. The average recoveries were in the range of 84.2-98.1% at different spiked levels (0.02, 0.04 and 0.08 mg kg(-1)), and the relative standard deviations were below 9.7%. The limits of quantification, calculated as 10 times the standard deviation, was 0.02 mg kg(-1). The developed method is simple, rapid, and accurate to quantitate the concentration of anthraquinone residues in tea samples.
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页数:9
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