Chen Pei
U.S. Department of Agriculture, Agricultural Research Service, Beltsville Human Nutrition Research Center, Food Composition Laboratory, Bldg 161, BARC-East, Beltsville, MD 20705, USA.
J AOAC Int. 2006 May-Jun;89(3):612-8.
A new, rapid, and reproducible reversed-phased liquid chromatography (LC) method with ultraviolet (UV) absorption and/or mass spectrometry (MS) detection has been developed and validated for quantitation of cichoric acid, a major constituent of Echinacea spp. The method involves the use of a short Phenomenex Hydro-RP C18 column (4 microm, 50 mm x 3.0 mm id) and a simple isocratic mobile phase profile. Both UV (diode array detector) and selective-ion monitoring (SIM) at m/z 472.8 were used for quantitation of cichoric acid. The limit of detection was 0.75 ng for UV and 0.15 ng for MS-SIM, and the limit of quantitation was is 2.5 ng for UV and 0.5 ng for MS-SIM. Water-methanol (1 + 1) soluble extracts of 6 commercially available Echinacea purpurea aerial parts-based dietary supplements (EPADS). EPADS were first profiled using a traditional HPLC-UV method. Their UV chromatograms were compared, and cichoric acid was identified to be a key biomarker for EPADS. Then the samples were analyzed by the fast LC-UV/MS method. The turnaround time for a single analysis was 3 min, compared to 15 to 60 min needed for traditional reported LC methods. The high-throughput method was able to separate the cichoric acid peak from peaks of other components in extracts of complex matrixes of EPADS.
已开发并验证了一种新的、快速且可重现的反相液相色谱(LC)方法,该方法采用紫外(UV)吸收和/或质谱(MS)检测,用于定量紫锥菊属植物的主要成分菊苣酸。该方法使用短的菲罗门Hydro-RP C18柱(4微米,50毫米×3.0毫米内径)和简单的等度流动相梯度。UV(二极管阵列检测器)和m/z 472.8处的选择性离子监测(SIM)均用于菊苣酸的定量。UV检测限为0.75纳克,MS-SIM检测限为0.15纳克,UV定量限为2.5纳克,MS-SIM定量限为0.5纳克。对6种市售紫锥菊地上部分膳食补充剂(EPADS)的水-甲醇(1 + 1)可溶性提取物进行分析。首先使用传统的HPLC-UV方法对EPADS进行分析。比较它们的UV色谱图,确定菊苣酸是EPADS的关键生物标志物。然后通过快速LC-UV/MS方法对样品进行分析。单次分析的周转时间为3分钟,而传统报道的LC方法需要15至60分钟。该高通量方法能够将菊苣酸峰与EPADS复杂基质提取物中其他成分的峰分开。