Faculty of Food and Biochemical Technology, Department of Food Chemistry and Analysis, Institute of Chemical Technology, Prague, Czech Republic.
Anal Bioanal Chem. 2012 Jul;403(10):2883-9. doi: 10.1007/s00216-012-5820-2. Epub 2012 Feb 15.
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.
本研究旨在展示一种快速方法的开发和应用,该方法采用直接实时分析(DART)离子源与高分辨率飞行时间质谱(TOFMS)相结合,用于定量分析各种咖啡样品中的咖啡因。采用热水进行简单的样品提取后,在环境质谱的优化条件下,直接进行高通量(<1 分钟/次运行)检测,无需任何预先的色谱分离。对于 DART-TOFMS 分析中的咖啡因定量,使用外部校准。使用同位素标记咖啡因来补偿咖啡因信号离子强度的变化。DART-TOFMS 方法的回收率在速溶咖啡的加标水平为 20 和 60mg/g 时分别为 97%,而对于烘焙研磨咖啡,在加标水平为 10 和 30mg/g 时,回收率分别为 106%和 107%。整个分析过程的重复性(表示为相对标准偏差,RSD,%)在所有测试的加标水平和基质中均<5%。由于该方法的线性范围相对较窄(两个数量级),因此需要在进行 DART-TOFMS 测量之前对样品进行稀释优化,以避免检测器饱和。