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

机译:稳定同位素稀释法-气相色谱-串联质谱法测定茶叶中的蒽醌

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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 chromatographytandem 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.
机译:这项研究的目的是开发一种分析方法,通过稳定同位素稀释测定-气相色谱串联质谱法(SIDA)准确测定茶叶样品(普'茶,乌龙茶,绿茶和红茶)中的蒽醌残留量。 -GC-MS / MS)。用正己烷:丙酮(1:1,v / v)萃取后,通过固相萃取纯化样品。然后通过选择的反应监测(SRM)以电子电离模式检测蒽醌残留。在茶叶样品提取过程中加入了蒽醌-d8,以消除基质效应。在不同的加标水平(0.02、0.04和0.08 mg kg〜(-1))下,平均回收率在84.2-98.1%的范围内,相对标准偏差在9.7%以下。以标准偏差的10倍计算的定量限为0.02 mg kg〜(-1)。所开发的方法简单,快速,准确,可以定量茶叶样品中蒽醌残留的浓度。

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