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

机译:与高效液相色谱(HPLC)和质谱联用的近红外光谱(NIRS)分析咖啡中的咖啡因,可可碱和茶碱

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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 (MS) detection.In this course non-porous silica-C18 showed to enable the analysis of the three alkaloids with high robustness within approx2.5 min,compared to 20min employing porous silica-C18 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-C18 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 Tbr in values for S.E.E.(standard error of estimation) of 0.34,0.40 g/100 g,S.E.R (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,NIRS 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.
机译:咖啡是国际贸易中最重要的原材料之一,需要最高的质量。由于要分析的样品数量很多,因此提供快速,可靠的质量数据的新分析技术至关重要。因此,我们建立了咖啡一种基于近红外光谱(NIRS)的新分析方法,用于将焙炒咖啡中的三种主要生物碱咖啡因(Caf),可可碱(Tbr)和茶碱(Tph)进行定量,然后将粗生豆分为阿拉伯和罗布斯塔。将经过验证的方法与连接到UV和质谱(MS)检测的最常用液相色谱(LC)进行比较。在此过程中,无孔硅胶C18显示出能够在约2.5的范围内对三种生物碱进行高稳健性分析与使用多孔二氧化硅C18作为固定相的20分钟相比,分析时间在选择近红外光谱仪的参考方法中起着重要作用r,无孔硅胶C18相提供了一种非常快速的方法。通过电喷雾电离(ESI)接口将优化的LC方法与质谱仪(MS)耦合,不仅可以根据其特征来识别Caf,Tbr和Tph使用碰撞诱导解离(CID)进行碎裂模式分析,同时还定量了三种分析物的含量,发现这三种分析物的含量比紫外检测高6%。经过验证的LC-UV方法被用作校准的参考方法对83种液体咖啡提取物进行随机分析,得出Caf和Tbr的SEE(估计标准误)值为0.34、0.40 g / 100 g,SER(预测标准误)为0.07和0.10 g / 100 g,相关系数为0.86和0.85,浓度范围在0.10和4.13 g / 100 g之间。与LC相比,NIRS方法的检测下限(LOD)为0.05 g / 100 g,而0.244 LC中为-0.60 ng / 100 g,这使得因此,主要的重点放在咖啡因和可可碱的NIRS分析上。尽管如此,NIRS还是咖啡生产行业中LC的重要替代品,因为它的分析时间短,只有几秒钟,并且保证了高样品通量。

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