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作 者:李利军[1] 孙科[1] 吴美艳[1] 罗应[1] 胡大春[1] 邓春燕[1] 李彦青[1]
机构地区:[1]广西工学院生物与化学工程系,广西柳州545006
出 处:《分析科学学报》2013年第2期154-158,共5页Journal of Analytical Science
基 金:国家自然科学基金(No.20665001);广西科学基金(No.0832062)
摘 要:建立了电堆集-场放大进样非水毛细管电泳法分离测定苦参中的槐定碱、苦参碱和氧化苦参碱。采用未涂层熔融石英毛细管(50cm×50μm i.d.,有效柱长36cm),紫外检测波长为209nm,运行缓冲溶液为50mmol/L乙酸铵-20%乙腈-0.75%乙酸-55%甲醇,分离电压20kV,电动进样20kV、15s,重力进水柱时间20s时达到最佳的分离效果。在优化条件下,上述三种生物碱均在15min内出峰,峰面积的相对标准偏差(RSD)均小于5%。检出限分别达到2.02μg/L、1.32μg/L和1.01μg/L。An electrostacking-field-amplified sample injection (FASI) method was used for the simultaneous separation and determination of sophoridine, matrine and oxymatrine in Sophora flavescens. The result indicated that a best separation of the three alkaloids was obtained on a uncoated fused silica capillary column(50 cm× 50 μm i. d., effective length 36 cm) by using the background electrolyte containing 50 mmol/L ammonium acetate,20% acetonitrile(by volume),0. 75% acetic acid (by volume) and 55% methanol(by volume). The detection wavelength was set at 209 nm, separation voltage was water was 2 the relative 20 kV,sample injection voltage was 20 0 s. Under the optimum conditions,the standard deviations of peak areas 1 kV and injection time was 15 s,and injection time three alkaloids were separated within 15 minutes w ess than sophoridine,matrine and oxymatrine were 2.02 μg/L,1.32 5%. The detection limits (S/N = 3) μg/L and 1.01μg/L,respectively. of th of
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