Analysis of caffeine, theobromine and theophylline in coffee by near infrared spectroscopy (NIRS) compared to high-performance liquid chromatography (HPLC) coupled to mass spectrometry

被引:153
作者
Huck, CW [1 ]
Guggenbichler, W [1 ]
Bonn, GK [1 ]
机构
[1] Leopold Franzens Univ, Inst Analyt Chem & Radiochem, A-6020 Innsbruck, Austria
关键词
coffee; caffeine; theobromine; theophylline; liquid chromatography; electrospray ionisation mass spectrometry; near infrared spectroscopy;
D O I
10.1016/j.aca.2005.01.064
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Coffee is one of the most important raw materials within the international trade, for which highest quality is demanded. Due to the high number of samples to be analysed, new analytical techniques providing fast and reliable data about the quality are essential. Therefore, we established a new analytical method based on near infrared spectroscopy (NIRS) for the quantitation of the three main alkaloids caffeine (Caf), theobromine (Tbr) and theophylline (Tph) in roasted coffee after discrimination of the rough green beans into Arabic and Robusta. This validated method was compared to the most commonly used liquid chromatography (LC) connected to UV and mass spectrometric (XIS) detection. In this course non-porous silica-C 18 showed to enable the analysis of the three alkaloids with high robustness within similar to 2.5 min, compared to 20 min employing porous silica-C 18 as a stationary phase. As analysis time plays an important role in choosing a reference method for the calibration of the NIR-spectrometer, the non-porous silica-C 18 phase offers a very fast method. Coupling of the optimised LC method to a mass spectrometer (MS) via an electrospray ionisation (ESI) interface not only allowed to identify Caf, Tbr and Tph by their characteristic fragmentation pattern using collisionally induced dissociation (CID), but also to quantitate the content of the three analytes, which was found to be 6% higher compared to UV-detection. The validated LC-UV method was chosen as a reference method for the calibration of the NIRS system. Analysis of 83 liquid coffee extracts in random order resulted for Caf and Thr in values for S.E.E. (standard error of estimation) of 0.34, 0.40 g/100 g, S.E.P. (standard error of prediction) of 0.07 and 0.10 g/100 g with correlation coefficients of 0.86 and 0.85 in a concentration range between 0.10 and 4.13 g/100 g. Compared to LC the lower limit of detection (LOD) of the NIRS-method is found at 0.05 g/100 g compared to 0.244-0.60 ng/100 g in LC, which makes it impossible to analyse Tph by NIRS. Therefore, main focus is put on the NIRS analysis of caffeine and theobromine. Nevertheless, NlRS offers a serious alternative to LC for the coffee producing industry because of the short analysis time of a few seconds and a guaranteed high sample throughput. (C) 2005 Elsevier BV. All rights reserved.
引用
收藏
页码:195 / 203
页数:9
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