Madison B L, Kozarek W J, Damo C P
J Assoc Off Anal Chem. 1976 Nov;59(6):1258-61.
A new method is described for the determination of caffeine in coffee, based on high-pressure liquid chromatography. The caffeine is extracted from the sample with water and/or methylene chloride, and then separated from interfering materials by passing an aliquot of the extract through a high-pressure column containing sulfonated cation exchange resin, using 0.01M nitric acid as the mobile phase. An ultraviolet detector measures the absorption of the solution directly. The method is rapid and eliminates the lengthy separations common to other methods. The procedure was applied successfully to decaffeinated and non-decaffeinated green, roasted, and instant coffees. This method gives a more accurate measure of the caffeine content in decaffeinated coffee samples than the micro Bailey-Andrew and modified Levine methods, with equal or better precision. This method gives results equal to those obtained by the official methods for non-decaffeinated samples.
描述了一种基于高压液相色谱法测定咖啡中咖啡因的新方法。咖啡因用水和/或二氯甲烷从样品中萃取出来,然后取一份萃取液通过装有磺化阳离子交换树脂的高压柱,以0.01M硝酸作为流动相,与干扰物质分离。用紫外检测器直接测量溶液的吸光度。该方法快速,消除了其他方法常见的冗长分离过程。该程序已成功应用于脱咖啡因和未脱咖啡因的生咖啡、烘焙咖啡和速溶咖啡。与微量贝利-安德鲁法和改良莱文法相比,该方法能更准确地测定脱咖啡因咖啡样品中的咖啡因含量,且精密度相同或更高。对于未脱咖啡因的样品,该方法给出的结果与官方方法得到的结果相当。