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首页> 外文期刊>Analytical and bioanalytical chemistry >Rapid analysis of caffeine in various coffee samples employing direct analysis in real-time ionization-high-resolution mass spectrometry
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Rapid analysis of caffeine in various coffee samples employing direct analysis in real-time ionization-high-resolution mass spectrometry

机译:使用实时电离-高分辨率质谱法中的直接分析快速分析各种咖啡样品中的咖啡因

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摘要

The development and use of a fast method employing a direct analysis in real time (DART) ion source coupled to high-resolution time-of-flight mass spectrometry (TOFMS) for the quantitative analysis of caffeine in various coffee samples has been demonstrated in this study. A simple sample extraction procedure employing hot water was followed by direct, high-throughput (<1 min per run) examination of the extracts spread on a glass rod under optimized conditions of ambient mass spectrometry, without any prior chromatographic separation. For quantification of caffeine using DART-TOFMS, an external calibration was used. Isotopically labeled caffeine was used to compensate for the variations of the ion intensities of caffeine signal. Recoveries of the DART-TOFMS method were 97% for instant coffee at the spiking levels of 20 and 60 mg/g, respectively, while for roasted ground coffee, the obtained values were 106% and 107% at the spiking levels of 10 and 30 mg/g, respectively. The repeatability of the whole analytical procedure (expressed as relative standard deviation, RSD, %) was <5% for all tested spiking levels and matrices. Since the linearity range of the method was relatively narrow (two orders of magnitude), an optimization of sample dilution prior the DART-TOFMS measurement to avoid saturation of the detector was needed.
机译:本文证明了一种快速方法的开发和使用,该方法采用实时直接分析(DART)离子源结合高分辨率飞行时间质谱(TOFMS)来定量分析各种咖啡样品中的咖啡因。研究。使用热水的简单样品提取程序之后,在优化的环境质谱分析条件下直接,高通量(每次运行<1分钟)检查分散在玻璃棒上的提取物,无需进行任何色谱分离。为了使用DART-TOFMS定量咖啡因,使用了外部校准。同位素标记的咖啡因用于补偿咖啡因信号的离子强度变化。在加料水平为20和60 mg / g时,速溶咖啡的DART-TOFMS方法的回收率分别为97%,而在加料水平为10和30的情况下,对于焙炒磨咖啡,回收率分别为106%和107%。毫克/克。对于所有测试的加标水平和基质,整个分析过程的重复性(表示为相对标准偏差,RSD,%)均小于5%。由于该方法的线性范围相对较窄(两个数量级),因此需要在DART-TOFMS测量之前优化样品稀释度以避免检测器饱和。

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