Pól Jaroslav, Hohnová Barbora, Hyötyläinen Tuulia
Laboratory of Analytical Chemistry, Department of Chemistry, University of Helsinki, P.O. Box 55, FIN-00014, Finland.
J Chromatogr A. 2007 May 25;1150(1-2):85-92. doi: 10.1016/j.chroma.2006.09.008. Epub 2006 Sep 25.
Comprehensive two-dimensional liquid chromatography (LC x LC) connected on-line to electrospray ionisation time-of-flight mass spectrometry (ESI-TOF-MS) was employed for analysis of aqueous extract of Stevia rebaudiana. Different combinations of strong cation-exchange (SCX), amino (NH2), and octadecyl siloxane (C18) stationary phases were tested in the separation of all nine known sweet Stevia glycosides. A combination of C18 as the first-dimension column and NH2 as the second-dimension column fully separated all the glycosides from the matrix. The method proved to be quantitative and repeatable. The limit of detection (S/N=3) for stevioside, a widely used natural sweetener, was 43.4 ng/g in dry leaves. The RSD for retention times was <0.1% and that of peak areas 4.5%.
将全二维液相色谱(LC×LC)与电喷雾电离飞行时间质谱(ESI-TOF-MS)在线联用,用于分析甜叶菊水提取物。在分离所有九种已知的甜叶菊糖苷时,测试了强阳离子交换(SCX)、氨基(NH2)和十八烷基硅氧烷(C18)固定相的不同组合。以C18作为第一维色谱柱和NH2作为第二维色谱柱的组合,可将所有糖苷与基质完全分离。该方法经证明具有定量性和可重复性。广泛使用的天然甜味剂甜菊糖苷的检测限(S/N=3)在干叶中为43.4 ng/g。保留时间的相对标准偏差(RSD)<0.1%,峰面积的相对标准偏差为4.5%。