化学
毛细管电泳
检出限
色谱法
吡哆醇
分析物
电化学
磷酸盐缓冲盐水
缓冲溶液
电极
褪黑素
工作电极
分析化学(期刊)
物理化学
医学
生物化学
内科学
作者
Gang Chen,Xianghuan Ding,Zhiguang Cao,Jiannong Ye
标识
DOI:10.1016/s0003-2670(99)00809-0
摘要
Melatonin (MT) and pyridoxine (PN) in pharmaceutical preparations for health-caring purposes were determined by capillary electrophoresis (CE) with electrochemical detection (ED). The effects of several factors such as acidity and concentration of running buffer, separation voltage and injection time on CE were investigated to acquire the optimum conditions. CE was performed in 0.025 mol/l phosphate buffer (pH 8.3). The two compounds were separated and detected within 12 min. The working electrode used was a 500-μm diameter carbon electrode operated in a wall-jet configuration. Excellent linearity was observed between peak current and concentration of analytes in the range from 2.5 × 10−6 to 1.0 × 10−3 mol/l for MT and from 5.0 × 10−6 to 1.0 × 10−3 mol/l for PN. The detection limits (S/N = 3) for MT and PN were 1.3 × 10−6 mol/l and 2.7 × 10−6 mol/l, respectively. The proposed method was successfully applied to analyze the actual samples with satisfactory assay results.
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