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Field-amplified sample stacking in capillary electrophoresis for the determination of alkaloids in Sinomenium acutum

机译:毛细管电泳中的场放大样品堆积法测定尖竹的生物碱

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摘要

An easy, rapid method for the simultaneous determination of isotetrandrine, curine, sinactine, sinomenine and magnof lorine in Sinomenium acutum was developed by a capillary electrophoresis (CE) method with field-amplified sample stacking (FASS). Parameters affecting CE separation and FASS performance were all carefully investigated to obtain the best sensitivity with the highest speed. Under the optimized conditions: UV detection at 214 nm, separation voltage 25 kV, 40 mM sodium citrate-citric acid (pH 3.5) as running buffer, the detection sensitivity was from 4.8 × 10~(-9) M to 1.0 × 10~(-8) M. This resulted in 20-100-fold improvement in concentration sensitivity relative to conventional capillary electrophoresis methods. The relative standard deviation (RSD) of the peak area ratios for repeatability (intraday, n = 5) and intermediate precision (interday, n = 5) were lower than 4.1% and 5.4%, respectively. Finally, the developed method was successfully applied to qualitatively and quantitatively analyze five alkaloids in Sinomenium acutum, with the recovery ranging from 75.5 to 102.2%.
机译:通过毛细管电泳(CE)和现场放大的样品堆叠(FASS)方法,建立了一种简便,快速的同时测定尖顶青霉中异丁防己碱,姜黄素,半胱氨酸,青藤碱和厚朴药水的方法。仔细研究了影响CE分离和FASS性能的参数,以最快的速度获得最佳灵敏度。在优化条件下:214 nm紫外检测,25 kV分离电压,40 mM柠檬酸钠-柠檬酸(pH 3.5)作为运行缓冲液,检测灵敏度为4.8×10〜(-9)M至1.0×10〜 (-8)M。与传统的毛细管电泳方法相比,这导致浓度灵敏度提高了20-100倍。重复性(盘中,n = 5)和中等精度(盘中,n = 5)的峰面积比的相对标准偏差(RSD)分别低于4.1%和5.4%。最终,该方法成功地用于定性和定量分析了尖竹的5种生物碱,回收率在75.5%至102.2%之间。

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