Xie Jianping, Zhang Jiyou, Liu Jiaqin, Tian Jianniao, Chen Xingguo, Hu Zhide
Department of Chemistry, Lanzhou University, Lanzhou 730000, PR China.
J Sep Sci. 2004 Oct;27(14):1211-4. doi: 10.1002/jssc.200401756.
A selective and sensitive micellar electrokinetic chromatography method with laser-induced fluorescence detection was developed for the quantification of ephedrine (E) and pseudoephedrine (PE) derivatized with 4-chloro-7-nitrobenzo-2-oxa-1,3-diazole. After conducting a series of optimizations, a running buffer of 10 mM sodium borate + 16 mM SDS was used for separation of the derivatives. A linear relationship for E and PE was obtained in the range of 0.044-6.6 microg mL(-1) (correlation coefficient: 0.9943 for E, 0.9946 for PE), and the detection limits for E and PE were 0.70 and 0.30 ng mL(-1), respectively. The sensitivity of E and PE was improved by several multiples of ten over those of CZE-LIF method. The method was applied to the analysis of the two alkaloids in ephedra herbal medicine and preparations with recoveries in the range of 98.3-107.1%.
建立了一种具有激光诱导荧光检测的选择性灵敏胶束电动色谱法,用于定量分析用4-氯-7-硝基苯并-2-恶唑-1,3-二唑衍生化的麻黄碱(E)和伪麻黄碱(PE)。经过一系列优化后,使用10 mM硼酸钠+16 mM十二烷基硫酸钠的运行缓冲液分离衍生物。E和PE在0.044-6.6 μg mL(-1)范围内呈线性关系(相关系数:E为0.9943,PE为0.9946),E和PE的检测限分别为0.70和0.30 ng mL(-1)。与毛细管区带电泳-激光诱导荧光法相比,E和PE的灵敏度提高了数十倍。该方法应用于麻黄草药和制剂中两种生物碱的分析,回收率在98.3-107.1%范围内。